Literature DB >> 24841313

Detection of Protein Posttranslational Modifications from Whole-Cell Extracts in Saccharomyces cerevisiae.

Lindsay G Ball1, Wei Xiao.   

Abstract

Saccharomyces cerevisiae is an ideal model organism as numerous cellular mechanisms are conserved in mammalian cells. This includes posttranslational modifications (PTMs) such as ubiquitination, sumoylation, and phosphorylation. For ubiquitination, target proteins are readily modified via a cascade reaction, which can result in various forms of ubiquitination known to be associated with numerous cellular mechanisms. Therefore it becomes imperative for researchers to detect PTMs of their favorite proteins in order to determine how the target proteins function and are regulated. However, detection of ubiquitination in vivo, as well as some other PTMs, has proven challenging for researchers due to the presence of deconjugating enzymes in the cell. This chapter describes a step-by-step protocol on how to preserve and subsequently detect PTMs of your favorite protein from budding yeast S. cerevisiae whole-cell extracts.

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Year:  2014        PMID: 24841313     DOI: 10.1007/978-1-4939-0799-1_19

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Sgs1 helicase is required for efficient PCNA monoubiquitination and translesion DNA synthesis in Saccharomyces cerevisiae.

Authors:  Fangfang Li; Lindsay G Ball; Li Fan; Michelle Hanna; Wei Xiao
Journal:  Curr Genet       Date:  2017-09-16       Impact factor: 3.886

  1 in total

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