H-1-NMR STRUCTURE AND BIOLOGICAL STUDIES OF THE HIS(23)-]CYS MUTANT NUCLEOCAPSID PROTEIN OF HIV-1 INDICATE THAT THE CONFORMATION OF THE FIRST ZINC-FINGER IS CRITICAL FOR VIRUS INFECTIVITY

Citation
H. Demene et al., H-1-NMR STRUCTURE AND BIOLOGICAL STUDIES OF THE HIS(23)-]CYS MUTANT NUCLEOCAPSID PROTEIN OF HIV-1 INDICATE THAT THE CONFORMATION OF THE FIRST ZINC-FINGER IS CRITICAL FOR VIRUS INFECTIVITY, Biochemistry, 33(39), 1994, pp. 11707-11716
Citations number
63
Categorie Soggetti
Biology
Journal title
ISSN journal
00062960
Volume
33
Issue
39
Year of publication
1994
Pages
11707 - 11716
Database
ISI
SICI code
0006-2960(1994)33:39<11707:HSABSO>2.0.ZU;2-M
Abstract
The nucleocapsid protein NCp7 of human immunodeficiency virus type 1 ( HIV-1), which has key functions in the virus life cycle, possesses two zinc fingers of the CX(2)CX(4)HX(4)C type characterized by three succ essive loops containing a tetrahedrally coordinated zinc atom, The rep lacement of any cysteine by a serine in either finger has been shown t o result in the production of noninfectious viruses, probably by impai ring the biological functions of NCp7. In order to more precisely eluc idate the structural role of the zinc finger motif, His(23) was replac ed by Cys in the proximal finger of the peptide (13-64)NCp7 which reta ins NCp7 activities in vitro. The peptide Cys(23)(13-64)NCp7 was synth esized by solid phase and studied by 2D H-1 NMR and molecular modeling . The His to Cys modification causes important structural modification s of the N-terminal zinc finger which impair the spatial proximity of the two zinc fingers as shown by the disappearance of several interres idue NOEs. The side chains of Val(13), Lys(14), Phe(16), Thr(24), Ala( 25), Trp(37), Gln(45), and Met(46), which are thought to be involved i n nucleic acid recognition, are no longer found clustered in the Cys(2 3)(13-64)NCp7 mutant as they are in the wild-type NCp7 structure. In v itro, Cys(23)(13-64)NCp7 is unable to tightly interact with the viral RNA or replication primer tRNA(Lys,3). The Cys(23)(NCp7) mutation was introduced into an infectious HIV-1 molecular clone, and virions produ ced upon DNA transfection into cells were analyzed for their viral pro tein and RNA compositions as well as for their infectivity. Results sh ow that, while the Cys(23)(NCp7) mutation does not impair virion produ ction, viruses contain a low amount of degraded viral RNA and are not infectious. These findings suggest that a bona fide conformation of th e HIV-1 NCp7 is critical for the packaging of viral RNA, its stability in virions, and virus infectivity.