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Quantitative proteomic identification of host factors involved in the salmonella typhimurium infection cycle

Research output: Chapter in Book/Report/Conference proceedingChapterAcademicpeer-review

Abstract

Quantitative proteomics, based on stable isotope labeling by amino acids in cell culture (SILAC), can be used to identify host proteins involved in the intracellular interplay with pathogens. This method allows identification of proteins subject to degradation or upregulation in response to intracellular infection. It can also be used to study intracellular dynamics (trafficking) of proteins in response to the infection. Here, we describe the analysis of changes in protein profiles determined in Golgi-enriched fractions isolated from cells that were either mock-infected or infected with Salmonella typhimurium. Using the SILAC approach we were able to identify 105 proteins in Golgi-enriched fractions that were significantly changed in their abundance as a result of Salmonella infection.

Original languageEnglish
Title of host publicationSalmonella
Subtitle of host publicationMethods and Protocols
PublisherSpringer New York
Pages29-45
Edition2
DOIs
Publication statusPublished - 1 Jan 2015

Publication series

NameMethods in molecular biology
PublisherHumana Press Inc.
Volume1225
ISSN (Print)1064-3745

Keywords

  • Cellular fractionation
  • Golgi membrane enrichment
  • Host–pathogen interactions
  • Salmonella typhimurium
  • SILAC

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