Discriminating small molecule DNA binding modes by single molecule force spectroscopy

被引:95
作者
Krautbauer, R
Pope, LH
Schrader, TE
Allen, S
Gaub, HE
机构
[1] Univ Munich, Lehrstuhl Angew Phys & CeNS, D-80799 Munich, Germany
[2] Univ Nottingham, Sch Pharmaceut Sci, Lab Biophys & Surface Anal, Nottingham NG7 2RD, England
基金
英国生物技术与生命科学研究理事会;
关键词
force spectroscopy; single molecule; DNA; small molecule binding; cisplatin; berenil; ethidium; bromide;
D O I
10.1016/S0014-5793(01)03257-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Drugs may interact with double stranded DNA via a variety of binding modes, each mode giving rise to a specific pharmacological function. Here we demonstrate the ability of single molecule force spectroscopy to discriminate between different interaction modes by measuring the mechanical properties of DNA and their modulation upon the binding of small molecules. Due to the unique topology of double stranded DNA and due to its base pair stacking pattern, DNA undergoes several well-characterised structural transitions upon stretching. We show that small molecule binding markedly affects these transitions in ways characteristic to the binding mode and that these effects can be detected at the level of an individual molecule. The minor groove binder berenil, the crosslinker cisplatin and the intercalator ethidium bromide are compared. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:154 / 158
页数:5
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