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Evosep Biosystems
Evosep Biosystems
Evosep develops new solutions to make clinical proteomics 100 times more robust and 10 times faster. We are basing our design on years of experience with nano-UHPLC R&D and application support, critically rethinking the necessary system architectures for successful sample separation before mass spectrometric analysis.
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Sample prep
LC/MS
LC/MS/MS
LC/TOF
LC/HRMS
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SEPSIS

RECORD | Already taken place Th, 23.2.2023
In this webinar we will uncover how our users combine technology with the Evosep One to further research into sepsis and its biomarkers.
Go to the webinar
Evosep: SEPSIS
Evosep: SEPSIS

Sepsis is a growing global challenge due to factors such as high mortality rate and the increasing prevalence of antimicrobial resistance.

A single and rapid Zeno SWATH DIA proteomic analysis for concomitant identification and antibiotic resistance profiling of micro-organisms from positive blood cultures

  • Presenter: Iulia MACAVEI, PhD (student in Analytical Chemistry, Biological Analysis and Mass Spectrometry, University of lyon)

Today, approximately 1.3 million people die each year worldwide from bacterial antimicrobial resistance (AMR). AMR is of great concern in the context of bloodstream infections (BSIs) when it evolves into sepsis. If MALDI-TOF has markedly shortened the delay of the pathogen identification step, AMR evaluation is still based on growth tests in the presence of antibiotics. With the aim of streamlining this turnaround time to less than 90min from a positive blood culture, the LC/Zeno SWATH DIA sensitivity and specificity performances were evaluated to concomitantly provide the identity and antibiotic resistance profile of etiological agents related to BSIs based on peptide surrogates.

Plasma proteomic landscape and patient heterogeneity in sepsis revealed by high-throughput mass spectrometry

  • Presenter: Dr. Yuxin Mi (Researcher at Wellcome Centre for Human Genetics, University of Oxford)

Incomplete knowledge of the sepsis plasma proteome has limited our understanding of pathophysiology in the heterogeneous syndrome of sepsis. Here we apply high-throughput liquid chromatography – tandem mass spectrometry to delineate the plasma proteome for sepsis and comparator groups, involving 2622 samples in a single batch. We show how this scale of data can establish shared and specific proteins, pathways and co-expression modules in sepsis, and be integrated with paired leukocyte transcriptomic data. This work reveals novel subphenotypes informative for the response state and differential outcome, highlighting opportunities for a systems-based precision medicine approach to sepsis.

Evosep Biosystems
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