Backbone equilibrium in mismatched DNA influenced by solution conditions

IF 2.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biophysical chemistry Pub Date : 2026-02-01 Epub Date: 2025-10-29 DOI:10.1016/j.bpc.2025.107548
A. Pilarski , Gary A. Meints
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引用次数: 0

Abstract

The impact of solution conditions on the 31P isotropic chemical shifts of DNA phosphates and therefore the sequence-dependent backbone conformational equilibrium has not been well-documented. There are no previous studies of DNA backbone equilibrium in the presence of crowding agents, nor any on mismatched DNA. A systematic study of several experimental conditions (Na+ concentration, K+ concentration, Mg2+ concentration, pH, the presence of PEG molecular crowders) was performed and the effect quantified in mismatched DNA compared to a canonical control sequence. Na+ concentration, pH and crowding agents have only a minimal effect on the backbone equilibrium (<5 % perturbation on backbone populations). But in the mismatched DNA, both K+ and Mg2+ shift the backbone equilibrium on both DNA strands but most significantly perturb the phosphates in proximity to the mismatch. This indicates a possible role of counterions in mismatch recognition or nucleotide flipping, and suggests knowledge of solutions conditions continue to be relevant for conformational processes.

Abstract Image

溶液条件对错配DNA主链平衡的影响
溶液条件对DNA磷酸盐的31P各向同性化学位移的影响以及序列依赖的主链构象平衡尚未得到充分的证明。以前没有关于拥挤剂存在下的DNA骨架平衡的研究,也没有关于错配DNA的研究。系统研究了几种实验条件(Na+浓度、K+浓度、Mg2+浓度、pH值、PEG分子聚集物的存在),并将错配DNA的影响与标准对照序列进行了量化。钠离子浓度、pH值和拥挤剂对骨架平衡的影响很小(对骨架种群的扰动为5%)。但在错配DNA中,K+和Mg2+都改变了两条DNA链上的主链平衡,但最显著的是干扰了错配DNA附近的磷酸盐。这表明反离子在错配识别或核苷酸翻转中的可能作用,并表明解决条件的知识仍然与构象过程相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biophysical chemistry
Biophysical chemistry 生物-生化与分子生物学
CiteScore
6.10
自引率
10.50%
发文量
121
审稿时长
20 days
期刊介绍: Biophysical Chemistry publishes original work and reviews in the areas of chemistry and physics directly impacting biological phenomena. Quantitative analysis of the properties of biological macromolecules, biologically active molecules, macromolecular assemblies and cell components in terms of kinetics, thermodynamics, spatio-temporal organization, NMR and X-ray structural biology, as well as single-molecule detection represent a major focus of the journal. Theoretical and computational treatments of biomacromolecular systems, macromolecular interactions, regulatory control and systems biology are also of interest to the journal.
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