HIV-1 REPRODUCTION IS INHIBITED BY PEPTIDES DERIVED FROM THE N-TERMINI AND C-TERMINI OF HIV-1 PROTEASE

被引:66
作者
SCHRAMM, HJ
NAKASHIMA, H
SCHRAMM, W
WAKAYAMA, H
YAMAMOTO, N
机构
[1] TOKYO MED & DENT UNIV,SCH MED,TOKYO 113,JAPAN
[2] UNIV MUNICH,HAMOSTASEOL ABT,W-8000 MUNICH 2,GERMANY
[3] YAMAGUCHI UNIV,SCH MED,DEPT VIROL & PARASITOL,YAMAGUCHI 753,JAPAN
关键词
D O I
10.1016/0006-291X(91)91895-J
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
Two octapeptides derived from the sequence of the N- and C-termini of HIV-1 protease were tested for their ability to inhibit HIV-1 reproduction. Weak inhibitory activity was found with each of the two peptides. It is assumed that HIV-1 protease is the target of the inhibitory action. In spite of the moderate inhibitory activity the results are encouraging since they may be improved by various means. © 1991.
引用
收藏
页码:847 / 851
页数:5
相关论文
共 10 条
[1]   SPECIFIC-INHIBITION OF HERPESVIRUS RIBONUCLEOTIDE REDUCTASE BY A NONAPEPTIDE DERIVED FROM THE CARBOXY TERMINUS OF SUBUNIT-2 [J].
COHEN, EA ;
GAUDREAU, P ;
BRAZEAU, P ;
LANGELIER, Y .
NATURE, 1986, 321 (6068) :441-443
[2]   SPECIFIC-INHIBITION OF HERPESVIRUS RIBONUCLEOTIDE REDUCTASE BY SYNTHETIC PEPTIDES [J].
DUTIA, BM ;
FRAME, MC ;
SUBAKSHARPE, JH ;
CLARK, WN ;
MARSDEN, HS .
NATURE, 1986, 321 (6068) :439-441
[3]   INFECTION OF HTLV-III/LAV IN HTLV-I-CARRYING CELLS MT-2 AND MT-4 AND APPLICATION IN A PLAQUE-ASSAY [J].
HARADA, S ;
KOYANAGI, Y ;
YAMAMOTO, N .
SCIENCE, 1985, 229 (4713) :563-566
[4]   INHIBITION OF HIV-1 PROTEASE IN INFECTED LYMPHOCYTES-T BY SYNTHETIC PEPTIDE ANALOGS [J].
MEEK, TD ;
LAMBERT, DM ;
DREYER, GB ;
CARR, TJ ;
TOMASZEK, TA ;
MOORE, ML ;
STRICKLER, JE ;
DEBOUCK, C ;
HYLAND, LJ ;
MATTHEWS, TJ ;
METCALF, BW ;
PETTEWAY, SR .
NATURE, 1990, 343 (6253) :90-92
[5]   DELETION OF SEQUENCES UPSTREAM OF THE PROTEINASE IMPROVES THE PROTEOLYTIC PROCESSING OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
PARTIN, K ;
ZYBARTH, G ;
EHRLICH, L ;
DECROMBRUGGHE, M ;
WIMMER, E ;
CARTER, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :4776-4780
[6]   SENSITIVE AND RAPID ASSAY ON MT-4 CELLS FOR DETECTION OF ANTIVIRAL COMPOUNDS AGAINST THE AIDS VIRUS [J].
PAUWELS, R ;
DECLERCQ, E ;
DESMYTER, J ;
BALZARINI, J ;
GOUBAU, P ;
HERDEWIJN, P ;
VANDERHAEGHE, H ;
VANDEPUTTE, M .
JOURNAL OF VIROLOGICAL METHODS, 1987, 16 (03) :171-185
[7]   RATIONAL DESIGN OF PEPTIDE-BASED HIV PROTEINASE-INHIBITORS [J].
ROBERTS, NA ;
MARTIN, JA ;
KINCHINGTON, D ;
BROADHURST, AV ;
CRAIG, JC ;
DUNCAN, IB ;
GALPIN, SA ;
HANDA, BK ;
KAY, J ;
KROHN, A ;
LAMBERT, RW ;
MERRETT, JH ;
MILLS, JS ;
PARKES, KEB ;
REDSHAW, S ;
RITCHIE, AJ ;
TAYLOR, DL ;
THOMAS, GJ ;
MACHIN, PJ .
SCIENCE, 1990, 248 (4953) :358-361
[8]  
SCHRAMM HJ, 1990, 8TH INT C VIR BERL P, V56
[9]  
SCHRAMM HJ, 1991, 7TH INT C AIDS FI MA, V1083
[10]   CONSERVED FOLDING IN RETROVIRAL PROTEASES - CRYSTAL-STRUCTURE OF A SYNTHETIC HIV-1 PROTEASE [J].
WLODAWER, A ;
MILLER, M ;
JASKOLSKI, M ;
SATHYANARAYANA, BK ;
BALDWIN, E ;
WEBER, IT ;
SELK, LM ;
CLAWSON, L ;
SCHNEIDER, J ;
KENT, SBH .
SCIENCE, 1989, 245 (4918) :616-621