Title | Affinity isolation and I-DIRT mass spectrometric analysis of the Escherichia coli O157:H7 Sakai RNA polymerase complex. |
Publication Type | Journal Article |
Year of Publication | 2008 |
Authors | Lee DJ, Busby SJW, Westblade LF, Chait BT |
Journal | J Bacteriol |
Volume | 190 |
Issue | 4 |
Pagination | 1284-9 |
Date Published | 2008 Feb |
ISSN | 1098-5530 |
Keywords | Blotting, 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. |
DOI | 10.1128/JB.01599-07 |
Alternate Journal | J Bacteriol |
PubMed ID | 18083804 |
Grant List | RR022220 / 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.