4.7 Article

Strain-Level Typing and Identification of Bacteria Using Mass Spectrometry-Based Proteomics

期刊

JOURNAL OF PROTEOME RESEARCH
卷 11, 期 5, 页码 2710-2720

出版社

AMER CHEMICAL SOC
DOI: 10.1021/pr2010633

关键词

LPI-FlowCell; mass spectrometry; proteomics; bacterial typing; bacterial identification

资金

  1. W.R. Wiley Environmental Molecular Science Laboratory
  2. U.S. Department of Energy's Office of Biological and Environmental Research and located at PNNL
  3. Battelle Memorial Institute for the U.S. Department of Energy [DE-AC05-76RL0 1830]
  4. Health & Medical Care Committee of the Regional Executive Board, Region Vastra Gotaland [72241]
  5. ALF-Medel for Forskning Projects [ALFGBG-11574, ALFGBG-210591]
  6. FoU-Vastra Gotaland Region Projects [VGFOUREG-30781, 83080, 157801]
  7. Wellcome Trust
  8. European Union
  9. Knut and Alice Wallenberg Foundation [KAW2007.0118]

向作者/读者索取更多资源

Because of the alarming expansion in the diversity and occurrence of bacteria displaying virulence and resistance to antimicrobial agents, it is increasingly important to be able to detect these microorganisms and to differentiate and identify closely related species, as well as different strains of a given species. In this study, a mass spectrometry proteomics approach is applied, exploiting lipid-based protein immobilization (LPI), wherein intact bacterial cells are bound, via membrane-gold interactions, within a FlowCell. The bound cells are subjected to enzymatic digestion for the generation of peptides, which are subsequently identified, using LC-MS. Following database matching, strain-specific peptides are used for subspecies-level discrimination. The method is shown to enable a reliable typing and identification of closely related strains of the same bacterial species, herein illustrated for Helicobacter pylori.

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