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表面如何影响杂交动力学。

How Surfaces Affect Hybridization Kinetics.

机构信息

Department of Chemical and Biomolecular Engineering, New York University Tandon School of Engineering, Brooklyn, New York 11201, United States.

出版信息

J Phys Chem B. 2021 Mar 25;125(11):2976-2986. doi: 10.1021/acs.jpcb.0c11400. Epub 2021 Mar 12.

DOI:10.1021/acs.jpcb.0c11400
PMID:33709715
Abstract

Hybridization between nucleic acid strands immobilized on a solid support with partners in solution is widely practiced in bioanalytical technologies and materials science. An important fundamental aspect of understanding these reactions is the role played by immobilization in the dynamics of duplex formation and disassembly. This report reviews and analyzes literature kinetic data to identify commonly observed trends and to correlate them with probable molecular mechanisms. The analysis reveals that while under certain conditions impacts from immobilization are minimal so that surface and solution hybridization kinetics are comparable, it is more typical to observe pronounced offsets between the two scenarios. In the forward (hybridization) direction, rates at the surface commonly decrease by one to two decades relative to solution, while in the reverse direction rates of strand separation at the surface can exceed those in solution by tens of decades. By recasting the deviations in terms of activation barriers, a consensus of how immobilization impacts nucleation, zipping, and strand separation can be conceived within the classical mechanism in which duplex formation is rate limited by preassembly of a nucleus a few base pairs in length, while dehybridization requires the cumulative breakup of base pairs along the length of a duplex. Evidence is considered for how excess interactions encountered on solid supports impact these processes.

摘要

核酸链在固体支持物上的杂交与溶液中的伴侣的杂交在生物分析技术和材料科学中得到了广泛的应用。理解这些反应的一个重要基本方面是固定化在双链体形成和拆卸动力学中的作用。本报告回顾和分析文献动力学数据,以确定常见的趋势,并将其与可能的分子机制相关联。分析表明,虽然在某些条件下,固定化的影响可以忽略不计,因此表面和溶液杂交动力学可以相比较,但更常见的是观察到两种情况之间明显的偏差。在正向(杂交)方向上,表面上的速率通常比溶液中的速率降低一个到两个数量级,而在反向方向上,表面上的链分离速率可以比溶液中的速率高出数十个数量级。通过根据活化能垒重新表述偏差,可以在经典机制中设想固定化如何影响成核、拉链和链分离,在该机制中,双链体的形成受到预组装几个碱基对长的核的速率限制,而去杂交则需要沿着双链体的长度累积打破碱基对。考虑了在固体支持物上遇到的多余相互作用如何影响这些过程的证据。

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