Studies on biomolecules using single molecule imaging and manipulation techniques

被引:4
作者
Harada, Y [1 ]
机构
[1] Tokyo Metropolitan Inst Med Sci, Dept Mol Physiol, JST, CREST,Bunkyo Ku, Tokyo 1138613, Japan
关键词
single molecule imaging; optical microscope; optical tweezers; fluorescent dye; RNA polymerase; DNA;
D O I
10.1016/j.stam.2004.02.014
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The best way to obtain unambiguous information about the function of biomolecules is to study their function at the single molecule level. By attaching a small tag such as a single fluorescent dye molecule to biomolecules, or a tag that is huge compared to the size of a biomolecule, we have been able to image the individual behaviours in real time under an optical microscope. Huge tags such as micrometer-sized plastic beads also allow the manipulation of individual molecules with, e.g. optical or magnetic tweezers. Using these techniques, we have observed individual behaviours, of RNA polymerase, a molecular machine that copies the genetic information on DNA onto a messenger RNA. We found that some of the RNA polymerase molecules underwent linear diffusion along DNA, helping RNA polymerase to search for the promoter. We also found that a single RNA polymerase molecule rotated around the right-handed screw axis of the double helix of DNA during transcription with a rotary torque of > 5 pN nm. The present methods are potentially applicable to the examination of a wide variety of protein-nucleic acid interactions, especially those involved in the process of transcription. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:709 / 713
页数:5
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