Disruption of energetic and dynamic base pairing cooperativity in DNA duplexes by an abasic site

被引:12
作者
Ashwood, Brennan [1 ,2 ]
Jones, Michael S. [3 ]
Ferguson, Andrew L. [3 ]
Tokmakoff, Andrei [1 ,2 ]
机构
[1] Univ Chicago, Inst Biophys Dynam, Dept Chem, Chicago, IL 60637 USA
[2] Univ Chicago, James Franck Inst, Chicago, IL 60637 USA
[3] Univ Chicago, Pritzker Sch Mol Engn, Chicago, IL 60637 USA
关键词
DNA; hybridization; cooperativity; molecular dynamics; time-resolved spectroscopy; MARKOV STATE MODELS; TEMPERATURE-JUMP; KINETICS; STABILITY; OLIGONUCLEOTIDES; HYBRIDIZATION; 8-OXOGUANINE; LESION; REPAIR;
D O I
10.1073/pnas.2219124120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA duplex stability arises from cooperative interactions between multiple adjacent nucleotides that favor base pairing and stacking when formed as a continuous stretch rather than individually. Lesions and nucleobase modifications alter this stability in complex manners that remain challenging to understand despite their centrality to biology. Here, we investigate how an abasic site destabilizes small DNA duplexes and reshapes base pairing dynamics and hybridization pathways using temperature-jump infrared spectroscopy and coarse-grained molecular dynamics simulations. We show how an abasic site splits the cooperativity in a short duplex into two segments, which destabilizes small duplexes as a whole and enables metastable half-dissociated configurations. Dynamically, it introduces an additional barrier to hybridization by constraining the hybridization mechanism to a step-wise process of nucleating and zipping a stretch on one side of the abasic site and then the other.
引用
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页数:10
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