Affinity isolation and I-DIRT mass spectrometric analysis of the Escherichia coli O157:H7 Sakai RNA polymerase complex.

TitleAffinity isolation and I-DIRT mass spectrometric analysis of the Escherichia coli O157:H7 Sakai RNA polymerase complex.
Publication TypeJournal Article
Year of Publication2008
AuthorsLee DJ, Busby SJW, Westblade LF, Chait BT
JournalJ Bacteriol
Volume190
Issue4
Pagination1284-9
Date Published2008 Feb
ISSN1098-5530
KeywordsBlotting, Western, Chromatography, Affinity, DNA-Directed RNA Polymerases, Electrophoresis, Polyacrylamide Gel, Escherichia coli O157, Escherichia coli Proteins, Gene Expression Regulation, Bacterial, Mass Spectrometry, Models, Biological, Protein Binding, Protein Subunits, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Tandem Mass Spectrometry
Abstract

Bacteria contain a single multisubunit RNA polymerase that is responsible for the synthesis of all RNA. Previous studies of the Escherichia coli K-12 laboratory strain identified a group of effector proteins that interact directly with RNA polymerase to modulate the efficiency of transcription initiation, elongation, or termination. Here we used a rapid affinity isolation technique to isolate RNA polymerase from the pathogenic Escherichia coli strain O157:H7 Sakai. We analyzed the RNA polymerase enzyme complex using mass spectrometry and identified associated proteins. Although E. coli O157:H7 Sakai contains more than 1,600 genes not present in the K-12 strain, many of which are predicted to be involved in transcription regulation, all of the identified proteins in this study were encoded on the "core" E. coli genome.

DOI10.1128/JB.01599-07
Alternate JournalJ Bacteriol
PubMed ID18083804
Grant ListRR022220 / RR / NCRR NIH HHS / United States
GM61898 / GM / NIGMS NIH HHS / United States
RR00862 / RR / NCRR NIH HHS / United States
/ WT_ / Wellcome Trust / United Kingdom
Related Faculty: 
Lars Westblade, Ph.D.

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