Force and velocity measured for single molecules of RNA polymerase

被引:706
作者
Wang, MD
Schnitzer, MJ
Yin, H
Landick, R
Gelles, J
Block, SM [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Princeton Univ, Princeton Mat Inst, Princeton, NJ 08544 USA
[3] Princeton Univ, Dept Phys, Princeton, NJ 08544 USA
[4] Brandeis Univ, Dept Biochem, Waltham, MA 02254 USA
[5] Univ Wisconsin, Dept Bacteriol, Madison, WI 53706 USA
关键词
D O I
10.1126/science.282.5390.902
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
RNA polymerase (RNAP) moves along DNA while carrying out transcription, acting as a molecular motor. Transcriptional velocities for single molecules of Escherichia coli RNAP were measured as progressively larger forces were applied by;a feedback-controlled optical trap. The shapes of RNAP force-velocity curves are distinct from those of the motor enzymes myosin or kinesin, and indicate that biochemical steps limiting transcription rates at Low loads do not generate movement. Modeling the data suggests-that high Loads may halt RNAP by promoting a structural change which moves all or part of the enzyme backwards through a comparatively Large distance, corresponding to 5 to 10 base pairs. This contrasts with previous models that assumed force acts directly upon a single-base translocation step.
引用
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页码:902 / 907
页数:6
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