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.
引用
收藏
页码:8984 / 8991
页数:8
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