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
相关论文
共 50 条
  • [21] HIV-1 nucleocapsid proteins as molecular chaperones for tetramolecular antiparallel g-quadruplex formation
    Endo, M. (endo@kuchem.kyoto-u.ac.jp), 1600, American Chemical Society (135):
  • [22] Major G-Quadruplex Form of HIV-1 LTR Reveals a (3+1) Folding Topology Containing a Stem-Loop
    Butovskaya, Elena
    Heddi, Brahim
    Bakalar, Blaz
    Richter, Sara N.
    Anh Tuan Phan
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (42) : 13654 - 13662
  • [23] U3 Region in the HIV-1 Genome Adopts a G-Quadruplex Structure in Its RNA and DNA Sequence
    Piekna-Przybylska, Dorota
    Sullivan, Mark A.
    Sharma, Gaurav
    Bambara, Robert A.
    BIOCHEMISTRY, 2014, 53 (16) : 2581 - 2593
  • [24] Structure-based HIV-1 integrase inhibitor design: a future perspective
    Neamati, N
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2001, 10 (02) : 281 - 296
  • [25] Structure-Based Predictors of Resistance to the HIV-1 Integrase Inhibitor Elvitegravir
    Masso, Majid
    Chuang, Grace
    Jain, Shinar
    Hao, Kate
    Vaisman, Iosif I.
    BIOPHYSICAL JOURNAL, 2014, 106 (02) : 409A - 409A
  • [26] Selective Recognition of a Single HIV-1 G-Quadruplex by Ultrafast Small-Molecule Screening
    Scalabrin, Matteo
    Nadai, Matteo
    Tassinari, Martina
    Lago, Sara
    Doria, Filippo
    Frasson, Ilaria
    Freccero, Mauro
    Richter, Sara N.
    ANALYTICAL CHEMISTRY, 2021, 93 (46) : 15243 - 15252
  • [27] Novel dimeric aryldiketo containing inhibitors of HIV-1 integrase: Effects of the phenyl substituent and the linker orientation
    Zeng, Li-Fan
    Jiang, Xiao-Hua
    Sanchez, Tino
    Zhang, Hu-Shan
    Dayam, Raveendra
    Neamati, Nouri
    Long, Ya-Qiu
    BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (16) : 7777 - 7787
  • [28] Structure-based predictors of resistance to the HIV-1 integrase inhibitor Elvitegravir
    Masso, Majid
    Chuang, Grace
    Hao, Kate
    Jain, Shinar
    Vaisman, Iosif I.
    ANTIVIRAL RESEARCH, 2014, 106 : 5 - 12
  • [29] Structure of the catalytic domain of avian sarcoma virus integrase with a bound HIV-1 integrase-targeted inhibitor
    Lubkowski, J
    Yang, F
    Alexandratos, J
    Wlodawer, A
    Zhao, H
    Burke, TR
    Neamati, N
    Pommier, Y
    Merkel, G
    Skalka, AM
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) : 4831 - 4836
  • [30] Structure of the catalytic domain of avian sarcoma virus integrase with a bound HIV-1 integrase-targeted inhibitor
    Lubkowski, J.
    Yang, F.
    Alexandratos, J.
    Wlodawer, A.
    Proceedings of the National Academy of Sciences of the United States of America, 95 (09):