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  • Woessmann, JakobKTH,Science for Life Laboratory, SciLifeLab,Systembiologi,Department of Biotechnology and Biomedicine, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark (författare)

Assessing the Role of Trypsin in Quantitative Plasma and Single-Cell Proteomics toward Clinical Application

  • Artikel/kapitelEngelska2023

Förlag, utgivningsår, omfång ...

  • American Chemical Society (ACS),2023
  • printrdacarrier

Nummerbeteckningar

  • LIBRIS-ID:oai:DiVA.org:kth-349635
  • https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-349635URI
  • https://doi.org/10.1021/acs.analchem.3c02543DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:ref swepub-contenttype
  • Ämneskategori:art swepub-publicationtype

Anmärkningar

  • QC 20240703
  • Mass spectrometry-based bottom-up proteomics is rapidly evolving and routinely applied in large-scale biomedical studies. Proteases are a central component of every bottom-up proteomics experiment, digesting proteins into peptides. Trypsin has been the most widely applied protease in proteomics due to its characteristics. With ever-larger cohort sizes and possible future clinical application of mass spectrometry-based proteomics, the technical impact of trypsin becomes increasingly relevant. To assess possible biases introduced by trypsin digestion, we evaluated the impact of eight commercially available trypsins in a variety of bottom-up proteomics experiments and across a range of protease concentrations and storage times. To investigate the universal impact of these technical attributes, we included bulk HeLa cell lysate, human plasma, and single HEK293 cells, which were analyzed over a range of selected reaction monitoring (SRM), data-independent acquisition (DIA), and data-dependent acquisition (DDA) instrument methods on three LC-MS instruments. The quantification methods employed encompassed both label-free approaches and absolute quantification utilizing spike-in heavy-labeled recombinant protein fragment standards. Based on this extensive data set, we report variations between commercial trypsins, their source, and their concentration. Furthermore, we provide suggestions on the handling of trypsin in large-scale studies.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Petrosius, ValdemarasDepartment of Biotechnology and Biomedicine, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark (författare)
  • Üresin, NilThe Finsen Laboratory, Rigshospitalet, Faculty of Health Sciences and Biotech Research and Innovation Centre (BRIC), University of Copenhagen, 2200 Copenhagen, Denmark (författare)
  • Kotol, DavidKTH,Systembiologi,Science for Life Laboratory, SciLifeLab(Swepub:kth)u1yd1hdh (författare)
  • Aragon-Fernandez, PedroDepartment of Biotechnology and Biomedicine, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark (författare)
  • Hober, Andreas,1992-KTH,Science for Life Laboratory, SciLifeLab,Systembiologi(Swepub:kth)u15bkxsl (författare)
  • Auf Dem Keller, UlrichDepartment of Biotechnology and Biomedicine, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark (författare)
  • Edfors, FredrikKTH,Science for Life Laboratory, SciLifeLab,Systembiologi(Swepub:kth)u149ml0e (författare)
  • Schoof, Erwin M.Department of Biotechnology and Biomedicine, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark (författare)
  • KTHScience for Life Laboratory, SciLifeLab (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Analytical Chemistry: American Chemical Society (ACS)95:36, s. 13649-136580003-27001520-6882

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