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DNA与蛋白质结合动力学40年错误的终结?

An end to 40 years of mistakes in DNA-protein association kinetics?

作者信息

Halford Stephen E

机构信息

Department of Biochemistry, The DNA-Proteins Interaction Unit, School of Medical Sciences, University of Bristol, Bristol, UK.

出版信息

Biochem Soc Trans. 2009 Apr;37(Pt 2):343-8. doi: 10.1042/BST0370343.

Abstract

Proteins that bind to specific sequences in long DNA molecules have to locate their target sites amid myriad alternative sequences, yet they do so at remarkably rapid rates, sometimes approaching 10(10) M(-1) x s(-1). Hence, it has been asserted widely that binding to specific DNA sites can surpass the maximal rate for 3D (three-dimensional) diffusion through solution and that this could only be accounted for by a reduction in the dimensionality of the search for the target in effect by 1D (one-dimensional) diffusion (or 'sliding') along the DNA contour. It will be shown here that there is, in fact, no known example of a protein binding to a specific DNA site at a rate above the diffusion limit, and that the rapidity of these reactions is due primarily to electrostatic interactions between oppositely charged molecules. It will also be shown that, contrary to popular belief, reduced dimensionality does not, in general, increase the rate of target-site location but instead reduces it. Finally, it will be demonstrated that proteins locate their target sites primarily by multiple dissociation/reassociation events to other (nearby or distant) sites within the same DNA molecule, and that 1D diffusion is limited to local searches covering approximately 50 bp around each landing site.

摘要

与长DNA分子中特定序列结合的蛋白质必须在无数的替代序列中找到其靶位点,但它们能以极快的速度做到这一点,有时接近10(10) M(-1)×s(-1)。因此,人们普遍认为,与特定DNA位点的结合可以超过通过溶液进行三维扩散的最大速率,而这只能通过实际上将寻找靶标的维度降低为沿DNA轮廓的一维扩散(或“滑动”)来解释。本文将表明,事实上,没有已知的蛋白质以高于扩散极限的速率与特定DNA位点结合的例子,并且这些反应的快速性主要是由于带相反电荷的分子之间的静电相互作用。还将表明,与普遍看法相反,维度降低通常不会提高靶位点定位的速率,反而会降低它。最后,将证明蛋白质主要通过与同一DNA分子内其他(附近或远处)位点的多次解离/重新结合事件来找到其靶位点,并且一维扩散仅限于围绕每个着陆位点覆盖约50个碱基对的局部搜索。

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