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Destabilization of i-Motif DNA at Neutral pH by G-Quadruplex Ligands
被引:27
|作者:
Abdelhamid, Mahmoud A. S.
[1
,2
]
Gates, Andrew J.
[2
,3
]
Waller, Zoe A. E.
[1
,2
]
机构:
[1] Univ East Anglia, Sch Pharm, Norwich Res Pk, Norwich NR4 7TJ, Norfolk, England
[2] Univ East Anglia, Ctr Mol & Struct Biochem, Norwich Res Pk, Norwich NR4 7TJ, Norfolk, England
[3] Univ East Anglia, Sch Biol Sci, Norwich Res Pk, Norwich NR4 7TJ, Norfolk, England
基金:
英国生物技术与生命科学研究理事会;
关键词:
SMALL-MOLECULE;
GENE PROMOTERS;
STABILITY;
SEQUENCES;
D O I:
10.1021/acs.biochem.8b00968
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Numerous studies have been published stressing the importance of finding ligands that can bind specifically to DNA secondary structures. Several have identified ligands that are presented as having specific binding to the G-quadruplex; however, these were not originally tested on the complementary i-motif structure. The i-motif was overlooked and presumed to be irrelevant due to the belief that the hemiprotonated (cytosine- cytosine) base pair at the core of the structure required acidic pH. The pathophysiological relevance of i-motifs has since been documented, as well as the discovery of several genomic sequences, which can form i-motif at neutral pH. Using different biophysical methodologies, we provide experimental evidence to show that widely used G-quadruplex ligands interact with i-motif structures at neutral pH, generally leading to their destabilization. Crucially, this has implications both for the search for quadruplex binding compounds as well as for the effects of compounds reported to have G-quadruplex specificity without examining their effects on i-motif.
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页码:245 / 249
页数:5
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