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Real time in vitro analysis of transcription by RNA polymerase on immobilized DNA fibres.

作者信息

Pemberton I K, Buckle M

机构信息

Unité de Physicochimie des Macromolécules Biologiques (URA 1149 du CNRS), Institut Pasteur, 25 Rue du Dr Roux, 75724 Paris cédex 15, France.

出版信息

J Mol Recognit. 1999 Sep-Oct;12(5):322-7. doi: 10.1002/(SICI)1099-1352(199909/10)12:5<322::AID-JMR471>3.0.CO;2-W.

Abstract

We have used surface plasmon resonance (SPR) to follow variations in the concentrations of binary complexes as RNA polymerase moves into a transcriptionally competent initiation complex with immobilized DNA fibres containing promoter sequences. The use of SPR to follow complex binding phenomena is described. We have also followed the changes in the mass of initiation complexes following addition of the nucleotide triphosphates prerequisite for transcription on the immobilized template. These signals are interpreted in terms of the escape of RNA polymerase into elongation mode and the subsequent synthesis of nascent RNA molecules.

摘要

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