Functional oligomeric state of avian sarcoma virus integrase

被引:59
作者
Bao, KK
Wang, H
Miller, JK
Erie, DA
Skalka, AM
Wong, I
机构
[1] Oregon State Univ, Dept Biochem & Biophys, Corvallis, OR 97331 USA
[2] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[3] Fox Chase Canc Ctr, Inst Canc Res, Philadelphia, PA 19111 USA
关键词
D O I
10.1074/jbc.C200550200
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
Retroviral integrase, one of only three enzymes encoded by the virus, catalyzes the essential step of inserting a DNA copy of the viral genome into the host during infection. Using the avian sarcoma virus integrase, we demonstrate that the enzyme functions as a tetramer. In presteady-state active site titrations, four integrase protomers were required for a single catalytic turnover. Volumetric determination of integrase-DNA complexes imaged by atomic force microscopy during the initial turnover additionally revealed substrate-induced assembly of a tetramer. These results suggest that tetramer formation may be a requisite step during catalysis with ramifications for antiviral design strategies targeting the structurally homologous human immunodeficiency virus, type 1 (HIV-1) integrase.
引用
收藏
页码:1323 / 1327
页数:5
相关论文
共 30 条
[21]   THE AVIAN RETROVIRAL IN PROTEIN IS BOTH NECESSARY AND SUFFICIENT FOR INTEGRATIVE RECOMBINATION INVITRO [J].
KATZ, RA ;
MERKEL, G ;
KULKOSKY, J ;
LEIS, J ;
SKALKA, AM .
CELL, 1990, 63 (01) :87-95
[22]   ENHANCED AND COORDINATED PROCESSING OF SYNAPSED VIRAL-DNA ENDS BY RETROVIRAL INTEGRASES IN-VITRO [J].
KUKOLJ, G ;
SKALKA, AM .
GENES & DEVELOPMENT, 1995, 9 (20) :2556-2567
[23]   IDENTIFICATION OF A HEXAPEPTIDE INHIBITOR OF THE HUMAN-IMMUNODEFICIENCY-VIRUS INTEGRASE PROTEIN BY USING A COMBINATORIAL CHEMICAL LIBRARY [J].
LUTZKE, RAP ;
EPPENS, NA ;
WEBER, PA ;
HOUGHTEN, RA ;
PLASTERK, RHA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11456-11460
[24]   Antiretroviral agents as inhibitors of both human immunodeficiency virus type 1 integrase and protease [J].
Mazumder, A ;
Wang, SM ;
Neamati, N ;
Nicklaus, M ;
Sunder, S ;
Chen, J ;
Milne, GWA ;
Rice, WG ;
Burke, TR ;
Pommier, Y .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (13) :2472-2481
[25]   Effect of HIV integrase inhibitors on the RAG1/2 recombinase [J].
Melek, M ;
Jones, JM ;
O'Dea, MH ;
Pais, G ;
Burke, TR ;
Pommier, Y ;
Neamati, N ;
Gellert, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :134-137
[26]   A novel single-molecule study to determine protein-protein association constants [J].
Ratcliff, GC ;
Erie, DA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (24) :5632-5635
[27]   CHARACTERIZATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INTEGRASE EXPRESSED IN ESCHERICHIA-COLI AND ANALYSIS OF VARIANTS WITH AMINO-TERMINAL MUTATIONS [J].
VINCENT, KA ;
ELLISON, V ;
CHOW, SA ;
BROWN, PO .
JOURNAL OF VIROLOGY, 1993, 67 (01) :425-437
[28]   Structure of a two-domain fragment of HIV-1 integrase: implications for domain organization in the intact protein [J].
Wang, JY ;
Ling, H ;
Yang, W ;
Craigie, R .
EMBO JOURNAL, 2001, 20 (24) :7333-7343
[29]   A minimal exonuclease domain of WRN forms a hexamer on DNA and possesses both 3′-5′ exonuclease and 5′-protruding strand endonuclease activities [J].
Xue, Y ;
Ratcliff, GC ;
Wang, H ;
Davis-Searles, PR ;
Gray, MD ;
Erie, DA ;
Redinbo, MR .
BIOCHEMISTRY, 2002, 41 (09) :2901-2912
[30]   Crystal structure of an active two-domain derivative of Rous sarcoma virus integrase [J].
Yang, ZN ;
Mueser, TC ;
Bushman, FD ;
Hyde, CC .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 296 (02) :535-548