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
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
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.