The capsid-spacer peptide 1 Gag processing intermediate is a dominant-negative inhibitor of HIV-1 maturation

被引:53
作者
Checkley, Mary Ann [1 ]
Luttge, Benjamin G. [1 ]
Soheilian, Ferri [2 ]
Nagashima, Kunio [2 ]
Freed, Eric O. [1 ]
机构
[1] NCI, Virus Cell Interact Sect, HIV Drug Resistance Program, Frederick, MD 21702 USA
[2] NCI, Image Anal Lab, Res Technol Program, SAIC Frederick, Frederick, MD 21702 USA
关键词
HIV-1; Gag; Virus maturation; Assembly; Retrovirus; Protease; HUMAN-IMMUNODEFICIENCY-VIRUS; TYPE-1; GAG; PARTICLE MATURATION; HELICAL STRUCTURE; VIRAL PROTEASE; CLEAVAGE SITES; LIFE-CYCLE; AMINO-ACID; POLYPROTEIN; CORE;
D O I
10.1016/j.virol.2010.01.028
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The human immunodeficiency virus type 1 (HIV-1) maturation inhibitor bevirimat disrupts virus replication by inhibiting the cleavage of the capsid-spacer peptide 1 (CA-SP1) Gag processing intermediate to mature CA. The observation that bevirimat delays but does not completely block CA-SP1 processing suggests that the presence of uncleaved CA-SP1 may disrupt the maturation process in trans. In this study, we validate this hypothesis by using a genetic approach to demonstrate that a non-cleavable CA-SP1 Mutant exerts a dominant-negative effect on Maturation of wild-type HIV-1. In contrast, a mutant in which cleavage can occur internally within SP1 is significantly less potent as a dominant-negative inhibitor. We also show that bevirimat blocks processing at both the major CA-SP1 cleavage site and the internal site. These data underscore the importance of full CA-SP1 processing for HIV-1 maturation and highlight the therapeutic potential of inhibitors that target this Gag cleavage event. Published by Elsevier Inc.
引用
收藏
页码:137 / 144
页数:8
相关论文
共 36 条
[1]   Efficient particle production by minimal gag constructs which retain the carboxy-terminal domain of human immunodeficiency virus type 1 capsid-p2 and a late assembly domain [J].
Accola, MA ;
Strack, B ;
Göttlinger, HG .
JOURNAL OF VIROLOGY, 2000, 74 (12) :5395-5402
[2]   A putative α-helical structure which overlaps the capsid-p2 boundary in the human immunodeficiency virus type 1 Gag precursor is crucial for viral particle assembly [J].
Accola, MA ;
Höglund, S ;
Göttlinger, HG .
JOURNAL OF VIROLOGY, 1998, 72 (03) :2072-2078
[3]   PRODUCTION OF ACQUIRED IMMUNODEFICIENCY SYNDROME-ASSOCIATED RETROVIRUS IN HUMAN AND NONHUMAN CELLS TRANSFECTED WITH AN INFECTIOUS MOLECULAR CLONE [J].
ADACHI, A ;
GENDELMAN, HE ;
KOENIG, S ;
FOLKS, T ;
WILLEY, R ;
RABSON, A ;
MARTIN, MA .
JOURNAL OF VIROLOGY, 1986, 59 (02) :284-291
[4]  
Adamson CS, 2007, ADV PHARMACOL, V55, P347, DOI 10.1016/S1054-3589(07)55010-6
[5]   In vitro resistance to the human immunodeficiency virus type 1 maturation inhibitor PA-457 (Bevirimat) [J].
Adamson, Catherine S. ;
Ablan, Sherimay D. ;
Boeras, Ioana ;
Goila-Gaur, Ritu ;
Soheilian, Ferri ;
Nagashima, Kunio ;
Li, Feng ;
Salzwedel, Karl ;
Sakalian, Michael ;
Wild, Carl T. ;
Freed, Eric O. .
JOURNAL OF VIROLOGY, 2006, 80 (22) :10957-10971
[6]  
ADAMSON CS, 2009, TARGETS, V13, P895
[7]   CLEAVAGE OF HIV-1 GAG POLYPROTEIN SYNTHESIZED INVITRO - SEQUENTIAL CLEAVAGE BY THE VIRAL PROTEASE [J].
ERICKSONVIITANEN, S ;
MANFREDI, J ;
VIITANEN, P ;
TRIBE, DE ;
TRITCH, R ;
HUTCHISON, CA ;
LOEB, DD ;
SWANSTROM, R .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1989, 5 (06) :577-591
[8]   SINGLE AMINO-ACID CHANGES IN THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 MATRIX PROTEIN BLOCK VIRUS PARTICLE-PRODUCTION [J].
FREED, EO ;
ORENSTEIN, JM ;
BUCKLERWHITE, AJ ;
MARTIN, MA .
JOURNAL OF VIROLOGY, 1994, 68 (08) :5311-5320
[9]   HIV-1 Gag proteins: Diverse functions in the virus life cycle [J].
Freed, EO .
VIROLOGY, 1998, 251 (01) :1-15
[10]   EVIDENCE FOR A FUNCTIONAL INTERACTION BETWEEN THE V1/V2 AND C4 DOMAINS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ENVELOPE GLYCOPROTEIN GP120 [J].
FREED, EO ;
MARTIN, MA .
JOURNAL OF VIROLOGY, 1994, 68 (04) :2503-2512