Early Folding Dynamics of i-Motif DNA Revealed by pH-Jump Time-Resolved X-ray Solution Scattering

被引:0
|
作者
Chan, Arnold M. [1 ,2 ]
Ebrahimi, Sasha B. [2 ,3 ]
Samanta, Devleena [1 ,2 ]
Leshchev, Denis [1 ]
Nijhawan, Adam K. [1 ,2 ]
Hsu, Darren J. [1 ]
Ho, Madeline B. [1 ]
Ramani, Namrata [2 ,4 ]
Kosheleva, Irina [5 ]
Henning, Robert [5 ]
Mirkin, Chad A. [1 ,2 ,3 ,4 ]
Kohlstedt, Kevin L. [1 ,2 ]
Chen, Lin X. [1 ,2 ,6 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem & Biomol Engn, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[5] Univ Chicago, Ctr Adv Radiat Sources, Chicago, IL 60637 USA
[6] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
STRUCTURAL DYNAMICS; STABILITY; PROMOTER; ASSOCIATION; PROTEINS;
D O I
10.1021/jacs.4c11768
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The i-motif is a pH-responsive cytosine-rich oligonucleotide sequence that forms, under acidic conditions, a quadruplex structure. This tunable structural switching has made the i-motif a useful platform for designing pH-responsive nanomaterials. Despite the widespread application of i-motif DNA constructs as biomolecular switches, the mechanism of i-motif folding on the atomic scale has yet to be established. We investigate the early folding structural dynamics of i-motif oligonucleotides with laser-pulse-induced pH-jump time-resolved X-ray solution scattering. Following the pH-jump, we observe that the initial random coil ensemble converts into a contracted intermediate state within 113 ns followed by further folding on the 10 ms time scale. We reveal the representative structures of these transient species, hitherto unknown, with molecular dynamics simulations and ensemble fitting. These results pave the way for understanding metastable conformations of i-motif folding and for benchmarking emerging theoretical models for simulating noncanonical nucleic acid structures.
引用
收藏
页码:33743 / 33752
页数:10
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