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HIV-1 integrase inhibitor T30177 forms a stacked dimeric G-quadruplex structure containing bulges
被引:85
|作者:
Mukundan, Vineeth Thachappilly
[1
]
Ngoc Quang Do
[1
,2
]
Anh Tuan Phan
[1
]
机构:
[1] Nanyang Technol Univ, Sch Phys & Math Sci, Singapore, Singapore
[2] Nanyang Technol Univ, Sch Biol Sci, Singapore, Singapore
关键词:
ANTI-HIV-1;
ACTIVITY;
POTENT INHIBITOR;
DNA QUADRUPLEX;
HUMAN TELOMERE;
LOOP-LENGTH;
OLIGONUCLEOTIDES;
SEQUENCE;
LONG;
SITE;
TETRAPLEX;
D O I:
10.1093/nar/gkr540
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:
T30177 is a G-rich oligonucleotide with the sequence (GTGGTGGGTGGGTGGGT) which inhibits the HIV-1 integrase activity at nanomolar concentrations. Here we show that this DNA sequence forms in K+ solution a dimeric G-quadruplex structure comprising a total of six G-tetrad layers through the stacking of two propeller-type parallel-stranded G-quadruplex subunits at their 5'-end. All twelve guanines in the sequence participate in the G-tetrad formation, despite the interruption in the first G-tract by a thymine, which forms a bulge between two adjacent G-tetrads. In this work, we also propose a simple analytical approach to stoichiometry determination using concentration-dependent melting curves.
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页码:8984 / 8991
页数:8
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