Two coexisting pseudo-mirror heteromolecular telomeric G-quadruplexes in opposite loop progressions differentially recognized by a low equivalent of Thioflavin T.
Two coexisting pseudo-mirror heteromolecular telomeric G-quadruplexes in opposite loop progressions differentially recognized by a low equivalent of Thioflavin T.
复制标题
两个共存的伪镜像异分子端粒 G 四链体在相反的环进程中被低当量的硫黄素 T 差异识别
DOI:
10.1093/nar/gkab755
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发表时间:
2021-10-11
影响因子:
14.9
通讯作者:
Zhang N
中科院分区:
文献类型:
--
作者:
Fu W;Jing H;Xu X;Xu S;Wang T;Hu W;Li H;Zhang N
The final 3′-terminal residue of the telomeric DNA G-overhang is inherently less precise. Here, we describe how alteration of the last 3′-terminal base affects the mutual recognition between two different G-rich oligomers of human telomeric DNA in the formation of heteromolecular G-quadruplexes (hetero-GQs). Associations between three- and single-repeat fragments of human telomeric DNA, target d(GGGTTAGGGTTAGGG) and probe d(TAGGGT), in Na+ solution yield two coexisting forms of (3 + 1) hybrid hetero-GQs: the kinetically favourable LLP-form (left loop progression) and the thermodynamically controlled RLP-form (right loop progression). However, only the adoption of a single LLP-form has been previously reported between the same probe d(TAGGGT) and a target variant d(GGGTTAGGGTTAGGGT) having one extra 3′-end thymine. Moreover, the flanking base alterations of short G-rich probe variants also significantly affect the loop progressions of hetero-GQs. Although seemingly two pseudo-mirror counter partners, the RLP-form exhibits a preference over the LLP-form to be recognized by a low equivalent of fluorescence dye thioflavin T (ThT). To a greater extent, ThT preferentially binds to RLP hetero-GQ than with the corresponding telomeric DNA duplex context or several other representative unimolecular GQs.
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DOI:
10.3390/molecules181012368
发表时间:
2013-10-08
期刊:
Molecules (Basel, Switzerland)
影响因子:
--
作者:
Bidzinska J;Cimino-Reale G;Zaffaroni N;Folini M
通讯作者:
Folini M
影响因子:
14.9
作者:
Brcic J;Plavec J
通讯作者:
Plavec J
影响因子:
15
作者:
Clore, GM;Kuszewski, J
通讯作者:
Kuszewski, J
影响因子:
14.9
作者:
Ambrus A;Chen D;Dai J;Bialis T;Jones RA;Yang D
通讯作者:
Yang D
影响因子:
48
作者:
Ivani I;Dans PD;Noy A;Pérez A;Faustino I;Hospital A;Walther J;Andrio P;Goñi R;Balaceanu A;Portella G;Battistini F;Gelpí JL;González C;Vendruscolo M;Laughton CA;Harris SA;Case DA;Orozco M
通讯作者:
Orozco M