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钾诱导的人端粒单链 DNA 中慢 G-四链体构象重排和可及性改变。

Slow G-Quadruplex Conformation Rearrangement and Accessibility Change Induced by Potassium in Human Telomeric Single-Stranded DNA.

机构信息

Department of Chemistry, University of Alabama at Birmingham, 901 14th Street South, Birmingham, Alabama 35294, United States.

出版信息

J Phys Chem B. 2024 Jun 27;128(25):5950-5965. doi: 10.1021/acs.jpcb.4c00719. Epub 2024 Jun 14.

Abstract

The guanine-rich telomeric repeats can form G-quadruplexes (G4s) that alter the accessibility of the single-stranded telomeric overhang. In this study, we investigated the effects of Na and K on G4 folding and accessibility through cation introduction and exchange. We combined differential scanning calorimetry (DSC), circular dichroism (CD), and single molecule Förster resonance energy transfer (smFRET) to monitor the stability, conformational dynamics, and complementary strand binding accessibility of G4 formed by single-stranded telomeric DNA. Our data showed that G4 formed through heating and slow cooling in K solution exhibited fewer conformational dynamics than G4 formed in Na solution, which is consistent with the higher thermal stability of G4 in K. Monitoring cation exchange with real time smFRET at room temperature shows that Na and K can replace each other in G4. When encountering high K at room or body temperature, G4 undergoes a slow conformational rearrangement process which is mostly complete by 2 h. The slow conformational rearrangement ends with a stable G4 that is unable to be unfolded by a complementary strand. This study provides new insights into the accessibility of G4 forming sequences at different time points after introduction to a high K environment in cells, which may affect how the nascent telomeric overhang interacts with proteins and telomerase.

摘要

富含鸟嘌呤的端粒重复序列可以形成 G-四链体 (G4s),改变单链端粒突出端的可及性。在这项研究中,我们通过引入和交换阳离子研究了 Na 和 K 对 G4 折叠和可及性的影响。我们结合差示扫描量热法 (DSC)、圆二色性 (CD) 和单分子Förster 共振能量转移 (smFRET) 来监测单链端粒 DNA 形成的 G4 的稳定性、构象动力学和互补链结合可及性。我们的数据表明,在 K 溶液中通过加热和缓慢冷却形成的 G4 比在 Na 溶液中形成的 G4 具有更少的构象动力学,这与 K 中 G4 的更高热稳定性一致。实时 smFRET 监测阳离子交换表明,Na 和 K 可以相互替代 G4 中的阳离子。当在室温或体温下遇到高 K 时,G4 会经历一个缓慢的构象重排过程,该过程在 2 小时内基本完成。缓慢的构象重排以无法被互补链展开的稳定 G4 结束。这项研究为细胞内引入高 K 环境后不同时间点 G4 形成序列的可及性提供了新的见解,这可能影响新生端粒突出端与蛋白质和端粒酶的相互作用方式。

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