Mapping of Protein-Protein Interactions of E. coli RNA Polymerase with Microfluidic Mechanical Trapping

被引:4
|
作者
Bates, Steven R. [1 ]
Quake, Stephen R. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[3] Stanford Univ, HHMI, Stanford, CA 94305 USA
来源
PLOS ONE | 2014年 / 9卷 / 03期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
ESCHERICHIA-COLI; MASS-SPECTROMETRY; ALPHA-SUBUNIT; CONTACT SITE; SIGMA-FACTOR; TRANSCRIPTION ACTIVATORS; IN-VITRO; REGION; YEAST; COMPLEX;
D O I
10.1371/journal.pone.0091542
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The biophysical details of how transcription factors and other proteins interact with RNA polymerase are of great interest as they represent the nexus of how structure and function interact to regulate gene expression in the cell. We used an in vitro microfluidic approach to map interactions between a set of ninety proteins, over a third of which are transcription factors, and each of the four subunits of E. coli RNA polymerase, and we compared our results to those of previous large-scale studies. We detected interactions between RNA polymerase and transcription factors that earlier high-throughput screens missed; our results suggest that such interactions can occur without DNA mediation more commonly than previously appreciated.
引用
收藏
页数:7
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