In closed communities such as the Amish in North America, rare genetic disorders occur more frequently. In children from this community, a condition has been described that affects the development of the nervous system and manifests, for example, as muscle weakness or epileptic seizures. The disorder is linked to a small change in a single protein, but for a long time it was unclear which cellular process this change disrupts. This question has now been answered by researchers from CEITEC Masaryk University, who show that the disease is caused by a disruption of a key mechanism required for the proper processing of genetic information in the cell.Every cell must first transcribe genetic information and then modify it before it can be used. From the original “working transcript,” unnecessary parts are removed and the remaining pieces are precisely joined together. This process, known as RNA splicing, consists of many consecutive steps and is tightly regulated. If the process does not proceed correctly or stops at any point, the cell cannot properly convert the copied genetic information into a usable form and therefore cannot function as it should.Researchers from CEITEC Masaryk University have now described one of the key steps in this process – a specific signal inside the cell. This signal acts as a checkpoint: only once it is fulfilled, the entire mechanism is activated and the process can continue.“We showed that during RNA splicing, a chemical modification of the protein SF3B1 is required at a precisely timed step. This modification allows another protein, SNIP1, to bind. If this signal is not transmitted correctly, the cell cannot proceed with the splicing process,” explains first author <a target="_blank" rel="noopener noreferrer" href="https://www.ceitec.eu/pavla-gajduskova-ph-d/u26136?page=publication">Pavla Gajdušková</a>.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CEITEC_Vzacna_geneticka_porucha_z_amisske_komunity_pomohla_potvrdit_klicovy_mechanismus_v_bunce_4_79e003984a.jpeg" alt="CEITEC: A Rare Genetic Disorder in the Amish Community Helped Confirm a Key Cellular Mechanism: Pavla Gajdušková" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_CEITEC_Vzacna_geneticka_porucha_z_amisske_komunity_pomohla_potvrdit_klicovy_mechanismus_v_bunce_4_79e003984a.jpeg 235w," sizes="100vw" width="1600" height="1067">This is where the research connects to patients in the Amish community. In affected children, a small genetic change in the SNIP1 protein disrupts its ability to respond properly to the signal mediated by the modified SF3B1 protein, making RNA splicing less efficient than in healthy individuals. As a result, errors occur during RNA splicing that the cell cannot correct, impairing its function – especially in the nervous system.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CEITEC_Vzacna_geneticka_porucha_z_amisske_komunity_pomohla_potvrdit_klicovy_mechanismus_v_bunce_44a7e2ef17.jpg" alt="CEITEC/Blažek Lab: A Rare Genetic Disorder in the Amish Community Helped Confirm a Key Cellular Mechanism: Interaction between SF3B1 and SNIP1 proteins." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_CEITEC_Vzacna_geneticka_porucha_z_amisske_komunity_pomohla_potvrdit_klicovy_mechanismus_v_bunce_44a7e2ef17.jpg 156w," sizes="100vw" width="1600" height="1600"><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CEITEC_Vzacna_geneticka_porucha_z_amisske_komunity_pomohla_potvrdit_klicovy_mechanismus_v_bunce_2_85826d711e.jpg" alt="CEITEC/Blažek Lab: A Rare Genetic Disorder in the Amish Community Helped Confirm a Key Cellular Mechanism: The effect of mutations in SNIP1 on cell proliferation." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_CEITEC_Vzacna_geneticka_porucha_z_amisske_komunity_pomohla_potvrdit_klicovy_mechanismus_v_bunce_2_85826d711e.jpg 235w," sizes="100vw" width="1600" height="1067">The researchers were thus able to clarify the cause of this rare neurodevelopmental disorder. “Additionally, the cause of this disease also confirms the correctness of the checkpoint we described. It shows that even a small change in one of the proteins involved can disrupt the RNA splicing mechanism on which the cell depends,” adds group leader <a target="_blank" rel="noopener noreferrer" href="https://www.ceitec.eu/dalibor-blazek-ph-d/u25918">Dalibor Blažek</a>.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CEITEC_Vzacna_geneticka_porucha_z_amisske_komunity_pomohla_potvrdit_klicovy_mechanismus_v_bunce_3_f95cfd68eb.jpeg" alt="CEITEC/Martin Indruch: A Rare Genetic Disorder in the Amish Community Helped Confirm a Key Cellular Mechanism: Dalibor Blažek." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_CEITEC_Vzacna_geneticka_porucha_z_amisske_komunity_pomohla_potvrdit_klicovy_mechanismus_v_bunce_3_f95cfd68eb.jpeg 235w," sizes="100vw" width="1600" height="1067">Although the study focuses on basic research, its implications are broader. It suggests that the same mechanism may also play a role in regulating cell division – a process that is often disrupted in cancer.<blockquote>The research was carried out by scientists from CEITEC Masaryk University in collaboration with researchers from Spain and Germany. The study was published in the journal <a target="_blank" rel="noopener noreferrer" href="https://www.nature.com/articles/s41467-026-71119-2">Nature Communications</a>.</blockquote>

A Rare Genetic Disorder in the Amish Community Helped Confirm a Key Cellular Mechanism

This study investigates the pathogenesis of neurosyphilis through cerebrospinal fluid proteomics using LC–MS/MS and ELISA validation. Comparative analysis identified 234 differentially expressed proteins, with major alterations linked to lysosomal dysfunction, axon guidance, and neurodegeneration pathways.Key lysosomal proteins, including PSAP and DNASE2, together with the axonal protein EPHA4, were significantly downregulated in neurosyphilis patients. These proteins showed potential as biomarkers for neurodegeneration and may provide new insights into disease mechanisms, diagnostics, and therapeutic targets.<blockquote><h4>The original article</h4><h4><a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689">Cerebrospinal Fluid Proteome Reveals Dysregulation of Lysosomal and Axonal Proteins in Neurosyphilis</a></h4>Huayang Tang*, Junjie Hu, Yifan Wu, Jinping Gao, Wenjun Wang, Xiaodong Zheng, Ran Zhang, Bo Liang, Fusheng Zhou, Ze Guo*J. Proteome Res. 2026, 25, 2, 713–722<a target="_blank" rel="noopener noreferrer" href="https://doi.org/10.1021/acs.jproteome.5c00689">https://doi.org/10.1021/acs.jproteome.5c00689</a><h6>licensed under <a target="_blank" rel="noopener noreferrer" href="https://creativecommons.org/licenses/by/4.0/">CC-BY 4.0</a></h6></blockquote>Selected sections from the article follow. Formats and hyperlinks were adapted from the original.<div>Neurosyphilis (NS) is a group of clinical syndromes characterized by neuroinflammation caused by Treponema pallidum (T. pallidum), which occurs in all stages of syphilis. <a href="javascript:void(0);">(1,2)</a> NS is classified based on clinical presentation as either asymptomatic (ANS) or symptomatic (SNS), and based on disease stage as either early (occurring 1–2 years after primary infection) or late. <a href="javascript:void(0);">(1)</a> T. pallidum can cause local nonspecific and central nervous system (CNS) inflammation, leading to possible degenerative changes. <a href="javascript:void(0);">(3)</a> The immune response of CNS in neurosyphilis is comparable to that observed in other neuroinflammatory diseases. Consequently, the presence of neurological symptoms may not reliably indicate active CNS inflammation in syphilis patients. <a href="javascript:void(0);">(3)</a> A cerebrospinal fluid (CSF) proteomic study identified three biomarkers (SEMA7A, SERPINA3, and ITIH4) that contribute to NS and have potential implications for diagnosis and therapeutic strategies. <a href="javascript:void(0);">(4)</a> Through integrated proteomics and single-cell transcriptomics analyses, Toll-like/NF-κB signaling was identified as the key pathway involved in CNS damage caused by T. pallidum. <a href="javascript:void(0);">(5)</a> Despite an increasing understanding of the biomarkers and possible neuroinflammatory damage mechanisms of neurosyphilis, the mechanisms of neurodegeneration caused by T. pallidum infection remain elusive. <a href="javascript:void(0);">(6)</a>Patients with neurosyphilis exhibit stage-specific profiles of soluble factors in their CSF, which are linked to both immune status and the extent of neuronal damage. <a href="javascript:void(0);">(7)</a> In this study, we analyzed differentially expressed proteins (DEPs) in the CSF proteomes from 28 individuals, including neurosyphilis (NS), suspected neurosyphilis (spNS) and non-neurosyphilis (nNS) individuals, by LC–MS/MS and analyzed a public data set of the neurosyphilis CSF proteome. Validation was then performed by ELISA in an independent group comprising 110 samples. The results revealed that neuroinflammation by T. pallidum infection results in dysregulation of the key proteins in lysosomal and axonal pathway, which suggesting a potential contribution to neurodegeneration in neurosyphilis.<h4>Materials and Methods</h4><h5>LC–MS/MS</h5>The tryptic peptides were dissolved in 0.1% formic acid (solvent A) and loaded onto a custom-made reversed-phase column (15 cm × 75 μm). Using an EASY-nLC 1000 UPLC system, a gradient was run at 400 nL/min as follows: 6% to 23% solvent B (0.1% formic acid in 98% acetonitrile) over 26 min, 23% to 35% in 8 min, up to 80% in 3 min, and held at 80% for 3 min. Peptides were ionized via an NSI source at 2.0 kV and analyzed online by a <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/559">Q Exactive Plus mass spectrometer</a>. Full scans (m/z 350–1800) were acquired in the Orbitrap at 70,000 resolution. The top precursors were selected for MS/MS with an NCE of 28, and fragments were detected at 17,500 resolution. A data-dependent method cycled between one MS scan and 20 MS/MS scans with a 15.0 s dynamic exclusion. AGC was set at 5E4. MS/MS data were processed with MaxQuant (v.1.5.2.8) using Trypsin/P as the enzyme (up to 2 missed cleavages). Precursor mass tolerance was 20 ppm (first search) and 5 ppm (main search); fragment mass tolerance was 0.02 Da. Fixed modification: carbamidomethyl (C); variable modification: oxidation (M). The FDR threshold was &lt;1%, and the minimum peptide score was &gt;40.<h5>ELISA</h5>CSF levels of host proteins were quantified using commercial ELISA kits according to the manufacturers’ protocols. Proteins analyzed included PSAP (OKEH07124, Aviva, USA), CTSL (abx150963, Abbexa, UK), NPC2 (A-QEK07857, Biogradetech, USA), and DNASE2 (abx386953, Abbexa, UK). Briefly, 100 μL of CSF was added to precoated plates and incubated at 37 °C for 2 h. After washing, 100 μL of detection antibody was added to each well and incubated at 37 °C for another 2 h. Following a wash, 100 μL of streptavidin-HRP working solution was added and incubated at room temperature for 20 min in the dark. The reaction was stopped with 50 μL of stop solution, and the optical density was measured at 450 nm.<h4>Results</h4><h5>Downregulation of Key Lysosomal Proteins in CSF from Patients With Neurosyphilis</h5>By analyzing the DEPs in NS vs nNS, we observed a significant enrichment of downregulated proteins in the lysosome pathway (P = 0.007) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>A), with 9 lysosomal proteins showing significant downregulation (Padj &lt; 0.05) in the NS group (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Table S4</a>). To validate this finding, we examined the public CSF proteomics data set of neurosyphilis (PXD033034) and identified 18 proteins in the lysosomal pathway that were significantly downregulated in patients with NS (Padj &lt; 0.05) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Table S4</a>). PPI network analysis determined the top 10 hub genes within the lysosome pathway (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>B). A Venn diagram revealed 3 proteins (PSAP, CTSL, and NPC2) shared across our current data, the public data set (PXD033034) and the top 10 hub genes (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>C). The mass spectrometry results indicated that the levels of PSAP (Padj = 0.043), CTSL (Padj = 0.028) and NPC2 (Padj = 0.013) were significantly lower in the NS group compared to the nNS group (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>D). The PXD033034 data set revealed consistent changes in the PSAP, CTSL, and NPC2 levels in the NS group (Padj &lt; 0.05) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Figure S1 and Table S4</a>). In addition, associations between the lysosomal protein DNASE2 and NS were observed in both the present study (Padj = 0.003) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>D) and the PXD033034 data set (Padj &lt; 0.05) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Figure S1 and Table S4</a>), with subgroup analysis revealing a significantly lower expression level of DNASE2 in the SNS group compared to the ANS group (P = 0.035) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>D and <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Table S3</a>). Further validation by ELISA (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Table S5</a>) in an independent group (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#tbl1">Table 1</a>) confirmed significantly downregulated CSF levels of PSAP (P &lt; 0.0001), CTSL (P &lt; 0.0001), NPC2 (P = 0.0024) and DNASE2 (P &lt; 0.0001) in patients with NS (n = 21) than in nNS individuals (n = 56) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>E) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Table S6</a>), as well as decreased in the SNS subgroup (P &lt; 0.05) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Figure S2 and Table S6</a>). Receiver operating characteristic (ROC) curve analysis supported PSAP (AUC = 0.91, 95% CI: 0.83–0.99) and DNASE2 (AUC = 0.95, 95% CI: 0.91–0.99) for distinguishing NS from nNS and as potential biomarkers for assessing neurodegeneration in NS (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>F). These results indicate that T. pallidum infection may lead to lysosomal dysfunction in CNS.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/J_Proteome_Res_2026_25_2_713_722_Figure_2_Downregulation_of_key_lysosomal_proteins_in_the_cerebrospinal_fluid_of_neurosyphilis_patients_bbccd95f44.jpg" alt="J. Proteome Res. 2026, 25, 2, 713–722: Figure 2. Downregulation of key lysosomal proteins in the cerebrospinal fluid of neurosyphilis patients. (a) KEGG pathway analysis demonstrated that downregulated proteins in patients with NS were significantly enriched in the lysosome pathway, as well as in axon guidance and neurodegeneration. (b) The top 10 hub genes involved in the lysosome pathway were identified using the STRING network data set and PPI analysis. (c) A Venn diagram revealed 3 proteins (PSAP, CTSL, and NPC2) shared across our current data, the public data set (PXD033034) and the top 10 hub genes. (d) The CSF levels of PSAP (Padj = 0.043), CTSL (Padj = 0.028), DNASE2 (Padj = 0.003) and NPC2 (Padj = 0.013) were significantly decreased in the NS group than in the nNS group. Subgroup analysis found a significantly lower expression level of DNASE2 in the SNS group than in the ANS group (P = 0.035). (e) PSAP, DNASE2, CTSL and NPC2 levels in CSF were tested by ELISA in the nNS (n = 56) and NS (n = 21) groups. Compared with those in the nNS group, significantly lower PSAP (P &lt; 0.0001), CTSL (P &lt; 0.0001), DNASE2 (P &lt; 0.0001) and NPC2 (P = 0.0024) levels were detected in the NS group. (f) ROC curve analysis for NS revealed that PSAP had an AUC = 0.91 (95% CI: 0.83–0.99), DNASE2 had an AUC = 0.95 (95% CI: 0.91–0.99), CTSL had an AUC = 0.85 (95% CI: 0.76–0.95), and NPC2 had an AUC = 0.72 (95% CI: 0.59–0.85). NS: neurosyphilis; nNS: non-neurosyphilis; ANS: asymptomatic neurosyphilis; SNS: symptomatic neurosyphilis. ROC: receiver operating characteristic; AUC: area under the curve. * P &lt; 0.05, ** P &lt; 0.01, ****P &lt; 0.0001." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_J_Proteome_Res_2026_25_2_713_722_Figure_2_Downregulation_of_key_lysosomal_proteins_in_the_cerebrospinal_fluid_of_neurosyphilis_patients_bbccd95f44.jpg 140w," sizes="100vw" width="2100" height="2339"><h5>Downregulation of Key Axonal Proteins Correlated with Lysosomal Protein Reduction in Neurosyphilis CSF</h5>Lysosomes play crucial roles in neuronal health by maintaining axonostasis. <a href="javascript:void(0);">(10)</a> The enrichment analysis indicated that the downregulated proteins in NS were implicated in the biological processes of axonostasis (such as axon development and axonogenesis) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig1">Figure 1</a>F) and the pathway of axon guidance (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig2">Figure 2</a>A). Our proteomic data revealed a total of 24 downregulated (Padj &lt; 0.05) axonal proteins and 1 upregulated (Padj &lt; 0.05) axonal protein in the CSF of patients with NS (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Table S9</a>). Furthermore, the PXD033034 data set revealed 55 downregulated (Padj &lt; 0.05) and 4 upregulated (Padj &lt; 0.05) axonal proteins in NS (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acs.jproteome.5c00689/suppl_file/pr5c00689_si_001.zip">Table S9</a>). The top 10 hub genes involved in the biological processes of axon development and axonogenesis were identified by PPI network analysis (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig4">Figure 4</a>A). Considering the overlap of our current data, the PXD033034 data set and the top 10 hub genes (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig4">Figure 4</a>B), one key protein, EPHA4, was identified across 3 data sets, with significant downregulation in our current data (Padj = 0.011) and in the PXD033034 data set (Padj = 0.028) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig4">Figure 4</a>C). Correlation analysis further revealed a positive correlation between the levels of PSAP and EPHA4 (r = i 0.83, P &lt; 0.05) (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jproteome.5c00689#fig4">Figure 4</a>D). Reduced levels of PSAP and EPHA4 in CSF have been implicated in neurodegenerative diseases, including Alzheimer’s disease (AD) and Parkinson’s disease (PD). <a href="javascript:void(0);">(11,12)</a> Our findings suggest that coordinated dysregulation of lysosomal and axonal proteins may contribute to neurodegeneration in NS.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/J_Proteome_Res_2026_25_2_713_722_Figure_4_Key_axonal_protein_downregulated_in_CSF_from_patients_with_neurosyphilis_66f5533e94.jpg" alt="J. Proteome Res. 2026, 25, 2, 713–722: Figure 4. Key axonal protein downregulated in CSF from patients with neurosyphilis. (a) The top 10 hub genes involved in axonostasis were identified by the STRING network data set and PPI analysis. (b) A Venn diagram revealed 1 protein (EPHA4) shared across DEPs related to axonostasis in our current data and in the public data set (PXD033034) and the top 10 hub genes. (c) EPHA4 was significantly downregulated both in our present study (Padj = 0.011) and in the PXD033034 data set (Padj = 0.028). (d) Correlation analysis demonstrated that the EPHA4 level was significantly positively correlated (P &lt; 0.05) with the levels of PSAP (r = 0.83), CTSL (r = 0.6), NPC2 (r = 0.69), DNASE2 (r = 0.61) and SEMA7A (r = 0.83). NS: neurosyphilis; nNS: non-neurosyphilis. * P &lt; 0.05." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_J_Proteome_Res_2026_25_2_713_722_Figure_4_Key_axonal_protein_downregulated_in_CSF_from_patients_with_neurosyphilis_66f5533e94.jpg 178w," sizes="100vw" width="1250" height="1096"><h4>Conclusions</h4>The present study reveals the associations of dysregulated proteins in lysosomal and axonal pathways with neurosyphilis, and potential evidence of shared pathophysiological mechanisms between neuroinflammation caused by T. pallidum infection and neurodegenerative diseases.However, this study has certain limitations. First, the use of ELISA to validate a limited number of proteins has certain limitations, such as the inherent cross-reactivity of ELISA. In the future, we can optimize the validation experiments by adding techniques such as Western blotting for verification. Second, this study uses a cross-sectional sampling method for research, which limits our ability to infer disease progression and treatment responses. In the future, we will conduct follow-up on the subjects, continue collecting cerebrospinal fluid samples after treatment, and observe whether the protein dysregulation is reversible after treatment. For spNS patients, follow-up should also be conducted to determine if they have transformed into NS, which will be very valuable for validating the predictive utility of our biomarkers. Finally, although multiple discovery and validation cohort studies have been conducted, we currently lack direct mechanistic evidence. Future work will investigate whether exposing neural cell coculture models to outer-membrane antigens of T. pallidum reproduces the lysosome and axon alterations observed in CSF, clarifying their role in neural damage of neurosyphilis and potential biomarkers for diagnosis and treatment of neurodegeneration in neurosyphilis.</div>

Cerebrospinal Fluid Proteome Reveals Dysregulation of Lysosomal and Axonal Proteins in Neurosyphilis

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Watrex Streamline™ P1 HPLC Pump, Stainless Steel

The Watrex Streamline™ P1 pump is a versatile and powerful dual-piston HPLC pump.

Streamline P1 pump, stainless steel fully meets the demanding requirements for HPLC pumps and can be combined seamlessly with HPLC detectors and instruments from other manufacturers.<blockquote>Price 4 935 € ex VAT</blockquote>In the analytical version of the pump, the flow rate range from 0.001 ml/min to 10 ml/min is adjustable in 1 ul increments with a maximum working pressure of 42 MPa (6,000 psi). Flow rate adjustment accuracy is ±1% and flow rate variation is better than ±0.1%. The pump’s extremely smooth flow profile is ensured by an efficient pulse damper and optimized cam shape.A unique feature is the active piston and seal rinse, which prevents crystallization of buffers. A touch screen display on the front panel allows intuitive control of the pump.The display shows the flow rate, the current pressure and the pump is equipped with pressure limits. A PRIME function is also directly available for flushing at increased flow rates.<figure class="image"><img style="aspect-ratio:611/408;" src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Streamline_P1_Pump_Stainless_Steel_23a7bf9f11.jpg" alt="Watrex: Streamline™ P1 Pump, Stainless Steel." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Watrex_Streamline_P1_Pump_Stainless_Steel_23a7bf9f11.jpg 234w," sizes="100vw" width="611" height="408"></figure><h3>TECHNICAL SPECIFICATION</h3><ul><li>Flow Rates: 0.001 to 10.000 mL/min</li><li>Pressure: 0 to 6,000 psi (42 MPa)</li><li>Flow precision: &gt; 0.2% RSD</li><li>Flow accuracy: ± 1 % @ 1mL/min and 7 MPa,</li><li>Pressure accuracy: ± 2% of full-scale, with 80:20 H2O/IPA @ 7 MPa</li><li>Pulsation: ± 0.5 % @ 1mL/min and 7 MPa</li><li>Remote inputs: USB</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/pumps/isocratic-pumps/streamline-p1-pump-stainless-steel/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Watrex Streamline™ UV1 HPLC detector, Stainless Steel

The Streamline™ UV1 HPLC detector offers an excellent signal-to-noise ratio, making it ideal for demanding applications.

Watrex Streamline™ UV1 programmable UV/VIS detector exhibits excellent signal-to-noise ratio for even the most demanding applications. It is equipped with standard analytical cell. It has a 2-lamp source (deuterium + tungsten), variable wavelength detector configuration suitable for operation between 190 and 800 nm.<blockquote>Price 4 788 € ex VAT</blockquote><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Watrex_Streamline_UV_1_UV_VIS_detector_686c6c9937.jpg" alt="Watrex: Streamline™ UV1 detector, Stainless Steel" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Watrex_Watrex_Streamline_UV_1_UV_VIS_detector_686c6c9937.jpg 245w," sizes="100vw" width="945" height="436"><h3>TECHNICAL SPECIFICATION</h3><ul><li>Light Source: Deuterium Lamp, Tungsten Lamp</li><li>Wavelength Range: 190 – 800 nm</li><li>Baseline Noise: 1 x 10-5 AU (@240 nm, 2 sec. risetime)</li><li>Baseline Drift: better than 3 x 10-4 AU/h</li><li>Wavelenghth Reproducibility: ± 0.1 nm</li><li>Linearity: better than 2.5 AU</li><li>Analog Output: 1x 1 V</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/detectors/uv-vis-detectors/streamline-uv1-detector/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Watrex Streamline™ PDA1 HPLC Detector, Stainless Steel

Photo-diode-array (PDA) HPLC detector with the optimum wavelength can be selected for each analyzed substance.

Watrex Streamline™ PDA1 is a photo-diode-array (PDA) detector for routine analysis and sophisticated research.<blockquote>Price 9 972 € ex VAT</blockquote>The dual lamp design offers a wavelength range of 190 – 720 nm (256 Diodes) with a low baseline noise.The front-accessible flow cell can easily bHPLCe exchanged, as can be the lamps which are accessible through a side panel in the instrument housing.Streamline™ PDA1 features 4-Wavelength channels to measure chromatograms at 4 different wavelengths at the same time. With this feature the optimum wavelength can be selected for each analyzed substance.<figure class="image"><img style="aspect-ratio:945/435;" src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Watrex_Streamline_PDA_1_Photodiode_array_detector_3784ec588b.jpg" alt="Watrex: Streamline™ PDA1 Detector, Stainless Steel" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Watrex_Watrex_Streamline_PDA_1_Photodiode_array_detector_3784ec588b.jpg 245w," sizes="100vw" width="945" height="435"></figure><h3>TECHNICAL SPECIFICATION</h3><ul><li>Wetted Materials: Stainless Steel/ PEEK*, teflon, Glass (*depending on configuration)</li><li>Light Source: Deuterium Lamp, Tungsten Lamp</li><li>Wavelength Range: 190 – 720 nm</li><li>Number of Diodes: 256</li><li>Baseline Noise: ± 1 x 10-5 AU (@240 nm, 1 sec. risetime)</li><li>Baseline Drift: better than 3 x 10-4 AU/h</li><li>Wavelength Accuracy: 0.5 nm</li><li>Mean Pixel Pitch: 2.2 nm</li><li>Resolution: 7 nm</li><li>Linearity: higher than 2.0 AU</li><li>Data Rate: 1 Hz – 100 Hz</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/detectors/uv-vis-detectors/streamline-pda1-detector-256-diodes/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Watrex Streamline RI1 Refractive index HPLC detector

The Watrex Streamline RI1 Refractive Index Detector is an essential component in high-performance liquid chromatography (HPLC) systems.

Streamline™ RI1 refractive index detector is suitable for detecting compounds with little or no UV activity such as alcohols, sugars, lipids or polymers. This instrument is designed for use in analytical HPLC (high performance liquid chromatography) as well as for GPC (gel permeation chromatography) applications.<h3>FEATURES</h3><ul><li>Advanced temperature control for high sensitivity and reproducibility</li><li>Prime purge valve</li><li>Long-life LED light source</li><li>Pressure resistant flow cell</li></ul><h3>TECHNICAL SPECIFICATION</h3><ul><li>Light Source: Long-life LED</li><li>Refractive index Range: 1.00 - 1.75 RIU</li><li>Baseline Noise: ± 2.5 nRIU</li><li>Baseline Drift: 200 nRIU/h</li><li>Linearity: &gt; 1000 μRIU</li><li>Flow cell pressure resistance: 5 bar</li><li>Flow cell volume: 15 μl</li><li>Time constant: 0.00/0.01/0.02/0.05/0.1/0.2/0.5/1.0/2.0/5.0/10.0 s</li><li>Analog Output: 1x 0-2.5V</li><li>Outputs: Event 1, Start (OUT), Error (OUT), + 5 V, 24 V Valve</li></ul><h3>Ordering information:</h3><h5>PN/Component:</h5><ul><li>SRI101-001 Watrex Streamline™ RI refractive index detector (Price 7 018 € ex VAT)</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/detectors/other-hplc-detectors/streamline-ri1-detector/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Watrex Streamline VD1 Viscosimetric HPLC detector

 Watrex Streamline™ VD1 viscosimetric detector is designed for detailed characterization of polymer compounds in both aqueous and organic solvents.

Streamline™ VD1 viscosimetric detector measures absolute intrinsic viscosity and is ideal as a detector for online monitoring in any GPC system. VD1 enables measurement of absolute molecular size using Wheatstone bridge operating principle.<h3>FEATURES</h3><ul><li>High sensitivity and stability</li><li>Low-noise</li><li>Open protocol digital data format</li><li>Direct dual analog output</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Watrex_Streamline_VD_1_Viscosimetric_detector_Universal_calibration_from_VD_1_data_1_149c741933.jpg" alt="Watrex: Watrex Streamline VD1 Viscosimetric detector - Universal calibration from VD1 data 1"><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Watrex_Streamline_VD_1_Viscosimetric_detector_Universal_calibration_from_VD_1_data_2_a616c498e8.jpg" alt="Watrex: Watrex Streamline VD1 Viscosimetric detector - Universal calibration from VD1 data 2"><h3>TECHNICAL SPECIFICATION</h3><ul><li>Wavelength Range: 190 – 720 nm</li><li>Baseline Noise: ± 1 x 10-5 AU (@240 nm, 2 sec. risetime)</li><li>Baseline Drift: &lt; 3 x 10-4 AU/h</li><li>Wavelength Accuracy: ± 0.5 nm</li><li>Wavelenghth Reproducibility: ± 0.1 nm</li><li>Mean Pixel Pitch: 2.2 nm</li><li>Resolution (λ FWHM): 7 nm</li><li>Linearity: &gt; 2.5 AU</li><li>Wavelength Program: Programmable, 10 steps</li><li>Analog Output (optional): 1x 1 V</li><li>Options: Dual channel configuration, thermostated flow cell</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Watrex_Streamline_VD_1_Viscosimetric_detector_Technical_specification_76756715f6.jpg" alt="Watrex: Watrex Streamline VD1 Viscosimetric detector - Technical specification"><h3>Ordering information:</h3><h5>PN/Component:</h5><ul><li>SVD101-001 Watrex Streamline™ VD1 viscosimetric detector (Price 19 741 € ex VAT)</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/detectors/other-hplc-detectors/streamline-vd1-detector/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Watrex Streamline CT1/CT1i HPLC Column thermostat

Watrex Streamline™ CT1i column thermostat is an ideal tool for maintaining stable separation temperatures.

Watrex Streamline CT1/CT1i column thermostat is an ideal tool to grant stable separation temperature even if laboratory temperature fluctuates during the day. It is also essential instrument in sugar analysis and/or many applications requiring higher column temperature. An optional built-in manual syringe front loaded sample injector increases usage comfort.<h3>FEATURES</h3><ul><li>Excellent temperature stability</li><li>Heating up to 100°C</li><li>Thermal fuse against overheating</li><li>Up to 3 columns with length of 250 mm can be placed in the thermostat</li><li>Color touch panel control</li><li>Possibility of installing manual injection valve</li></ul><h3>TECHNICAL SPECIFICATION</h3><ul><li>Temperature range: 10 °C above ambient temperature to 100 °C</li><li>Temperature accuracy: max. 0,5 % of actual temperature</li><li>Temperature stability: RSD &lt; 0,4 %</li><li>Settability: 0,1 °C</li><li>Internal dimensions: 320 x 50 x 30 mm (L x W x H)</li><li>Compartment material: PTFE coated metal</li><li>Compartment connection: USB</li><li>Control: build-in color touch panel, datasystem</li></ul><h3>Ordering information:</h3><h5>PN/Component:</h5><ul><li>ST101-001 Streamline CT1 Columm Thermostat (Price 1 720 € ex VAT)</li><li>ST101-002 Streamline CT1i Columm Thermostat with manual injector</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/column-thermostats/streamline-ct1-columm-thermostat/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Watrex Streamline™ P1 HPLC Pump, PEEK

Streamline P1 pump, PEEK fully meets the demanding requirements for HPLC pumps and can be combined seamlessly with HPLC detectors and instruments from other manufacturers.<blockquote>Price 4 935 € ex VAT</blockquote>In the analytical version of the pump, the flow rate range from 0.001 ml/min to 10 ml/min is adjustable in 1 ul increments with a maximum working pressure of 42 MPa (6,000 psi). Flow rate adjustment accuracy is ±1% and flow rate variation is better than ±0.1%. The pump’s extremely smooth flow profile is ensured by an efficient pulse damper and optimized cam shape.A unique feature is the active piston and seal rinse, which prevents crystallization of buffers. A touch screen display on the front panel allows intuitive control of the pump.The display shows the flow rate, the current pressure and the pump is equipped with pressure limits. A PRIME function is also directly available for flushing at increased flow rates.<figure class="image"><img style="aspect-ratio:1024/768;" src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Streamline_P1_Pump_PEEK_dbc4418900.jpg" alt="Watrex: Streamline™ P1 Pump, PEEK." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Watrex_Streamline_P1_Pump_PEEK_dbc4418900.jpg 208w," sizes="100vw" width="1024" height="768"></figure><h3>TECHNICAL SPECIFICATION</h3><ul><li>Flow Rates: 0.001 to 10.000 mL/min</li><li>Pressure: 0 to 6,000 psi (42 MPa)</li><li>Flow precision: &gt; 0.2% RSD</li><li>Flow accuracy: ± 1 % @ 1mL/min and 7 MPa,</li><li>Pressure accuracy: ± 2% of full-scale, with 80:20 H2O/IPA @ 7 MPa</li><li>Pulsation: ± 0.5 % @ 1mL/min and 7 MPa</li><li>Remote inputs: USB</li></ul>

Watrex Streamline™ PDA1 HPLC Detector, PEEK

Watrex Streamline™ PDA1 is a photo-diode-array (PDA) detector for routine analysis and sophisticated research.<blockquote>Price 9 972 € ex VAT</blockquote>The dual lamp design offers a wavelength range of 190 – 720 nm (256 Diodes) with a low baseline noise.The front-accessible flow cell can easily be exchanged, as can be the lamps which are accessible through a side panel in the instrument housing.Streamline™ PDA1 features 4-Wavelength channels to measure chromatograms at 4 different wavelengths at the same time. With this feature the optimum wavelength can be selected for each analyzed substance.<figure class="image"><img style="aspect-ratio:945/435;" src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Watrex_Streamline_PDA_1_Photodiode_array_detector_3784ec588b.jpg" alt="Watrex: Streamline™ PDA1 Detector, Stainless Steel" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Watrex_Watrex_Streamline_PDA_1_Photodiode_array_detector_3784ec588b.jpg 245w," sizes="100vw" width="945" height="435"></figure><h3>TECHNICAL SPECIFICATION</h3><ul><li>Wetted Materials: Stainless Steel/ PEEK*, teflon, Glass (*depending on configuration)</li><li>Light Source: Deuterium Lamp, Tungsten Lamp</li><li>Wavelength Range: 190 – 720 nm</li><li>Number of Diodes: 256</li><li>Baseline Noise: ± 1 x 10-5 AU (@240 nm, 1 sec. risetime)</li><li>Baseline Drift: better than 3 x 10-4 AU/h</li><li>Wavelength Accuracy: 0.5 nm</li><li>Mean Pixel Pitch: 2.2 nm</li><li>Resolution: 7 nm</li><li>Linearity: higher than 2.0 AU</li><li>Data Rate: 1 Hz – 100 Hz</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/detectors/uv-vis-detectors/streamline-pda1-detector-256-diodes-2/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Watrex Streamline™ UV1 HPLC detector, PEEK

The Streamline™ UV1 detector offers an excellent signal-to-noise ratio, making it ideal for demanding applications.

Watrex Streamline™ UV1 programmable UV/VIS detector exhibits excellent signal-to-noise ratio for even the most demanding applications. It is equipped with standard analytical cell. It has a 2-lamp source (deuterium + tungsten), variable wavelength detector configuration suitable for operation between 190 and 800 nm.<blockquote>Price 4 788 € ex VAT</blockquote><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Watrex_Streamline_UV_1_UV_VIS_detector_686c6c9937.jpg" alt="Watrex: Streamline™ UV1 detector, PEEK" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Watrex_Watrex_Streamline_UV_1_UV_VIS_detector_686c6c9937.jpg 245w," sizes="100vw" width="945" height="436"><h3>TECHNICAL SPECIFICATION</h3><ul><li>Light Source: Deuterium Lamp, Tungsten Lamp</li><li>Wavelength Range: 190 – 800 nm</li><li>Baseline Noise: 1 x 10-5 AU (@240 nm, 2 sec. risetime)</li><li>Baseline Drift: better than 3 x 10-4 AU/h</li><li>Wavelenghth Reproducibility: ± 0.1 nm</li><li>Linearity: better than 2.5 AU</li><li>Analog Output: 1x 1 V</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/detectors/uv-vis-detectors/streamline-uv1-detector-2/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Watrex Streamline™ Binary High Pressure Gradient system, PEEK

Binary high pressure gradient Streamline system in PEEK version, consisting of two P1m+P1s pumps with programmable mixing of two mobile phase components at high pressure with 0.1% accuracy.

Binary high pressure gradient Streamline system in PEEK version, consisting of two P1m+P1s pumps with programmable mixing of two mobile phase components at high pressure with 0.1% accuracy (between 10% and 90% mixing ratios).<blockquote>Price 9 333 € ex VAT</blockquote>An integrated two-channel degasser is a recommended part locvated on the top in the solvent cabinet. In the analytical version, the flow rate range from 0.001 ml/min to 10 ml/min is adjustable to 0.001 ml/min accuracy with a maximum working pressure of 35 MPa (5,000 psi). Flow rate adjustment accuracy is ±1% and flow rate variation is better than ±0.1%. A unique feature is an active piston and seal rinse that prevents crystallization of buffers.A touch screen display on the front panel allows intuitive control of the pump. The display shows the flow rate. A PRIME function is also directly available for flushing at increased flow rates. A cabinet is included for placing bottles with mobile phases. Control and programming of the gradient is done from the Clarity data station.<figure class="image"><img style="aspect-ratio:800/600;" src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Watrex_Streamline_P1q_HPLC_Pump_PEEK_c4ca5fdaa4.jpg" alt="Watrex: Streamline™ Binary High Pressure Gradient system, PEEK" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Watrex_Streamline_P1q_HPLC_Pump_PEEK_c4ca5fdaa4.jpg 208w," sizes="100vw" width="800" height="600"></figure><h3>PUMP FEATURES</h3><ul><li>Each pump has a single stepper motor driven, dual head positive displacement pump (pump heads 180° out of phase)</li><li>PEEK pump heads and fluid path</li><li>Incorporates a diaphragm-type pulse damper, which reduces pulsation in the system by as much as 90% and includes an isolated pressure transducer (i.e., the transducer adds no dead volume).</li><li>Ruby/Sapphire Check Valves (1/16” ball)</li><li>Front panel flow adjustment in 0.001 mL/min increments</li><li>Upper and Lower Pressure Limits: Automatically turns the pump OFF if the system pressure exceeds the maximum pressure limit, or drops below minimum pressure limit</li><li>Microprocessor advanced control with advanced pre-compression algorithm and user calibration feature</li><li>Back panel USB communications port for complete control and status monitoring; Clarity Driver available</li><li>Automatic piston wash (self-flush)</li></ul><h3>TECHNICAL SPECIFICATION</h3><ul><li>Flow Rates: 0.001 ml/min – 10 ml/min with step 0.001 ml/min</li><li>Pressure: 35 MPa/5000 psi</li><li>Pulsation: ± 1% @ from 7 MPa to 42 MPa</li><li>Pressure Accuracy: ± 2% of full-scale, with IPA</li><li>Flow Accuracy:&nbsp;better than ± 1% @ 10mL/min</li><li>Flow Precision: better then 0.1% RSD or 0.2 min SD, whichever is greater, across the full flow range, 20 MPa, with degassed methanol</li><li>Remote control: USB</li><li>I/O connector:&nbsp;Start, Stop, Status, Error</li></ul>You can also visit this product on the <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/obchod/chromatography/pumps/gradient-pumps/streamline-binary-high-pressure-gradient-system-peek/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex website</a>.

Products focused on HPLC from Watrex Prague - page 2

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