COMPARISON OF THE HIV-1 AND HIV-2 PROTEINASES USING OLIGOPEPTIDE SUBSTRATES REPRESENTING CLEAVAGE SITES IN GAG AND GAG-POL POLYPROTEINS

被引:143
|
作者
TOZSER, J [1 ]
BLAHA, I [1 ]
COPELAND, TD [1 ]
WONDRAK, EM [1 ]
OROSZLAN, S [1 ]
机构
[1] NCI, FREDERICK CANC RES & DEV CTR, ABL BASIC RES PROGRAM, MOLEC VIROL & CARCINOGENESIS LAB,POB B, FREDERICK, MD 21702 USA
来源
FEBS LETTERS | 1991年 / 281卷 / 1-2期
关键词
HIV-1; PROTEINASE; HIV-2; OLIGOPEPTIDE SUBSTRATE; ENZYME KINETICS; SUBSTRATE SPECIFICITY;
D O I
10.1016/0014-5793(91)80362-7
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
The substrate specificity of the human immunodeficiency virus type 1 (HIV-1) and type 2 (HIV-2) proteinases was compared using oligopeptides corresponding to cleavage sites in the Gag and Gag-Pol polyproteins of both viruses. All peptides mimicking cleavage sites at the junction of major functional protein domains were correctly cleaved by both enzymes. However, some other peptides thought to represent secondary cleavage sites remained intact. The kinetic parameters (K(m) and k(cat)) obtained for the different substrates showed several hundred-fold variation but were similar for the same substrate.
引用
收藏
页码:77 / 80
页数:4
相关论文
共 50 条
  • [1] Effects of reduced gag cleavage efficiency on HIV-1 Gag-Pol package
    Yi-Ru Lin
    Shih-Ming Chu
    Fu-Hsien Yu
    Kuo-Jung Huang
    Chin-Tien Wang
    BMC Microbiology, 22
  • [2] Effects of reduced gag cleavage efficiency on HIV-1 Gag-Pol package
    Lin, Yi-Ru
    Chu, Shih-Ming
    Yu, Fu-Hsien
    Huang, Kuo-Jung
    Wang, Chin-Tien
    BMC MICROBIOLOGY, 2022, 22 (01)
  • [3] Modulation of HIV-1 Gag/Gag-Pol frameshifting by tRNA abundance
    Korniy, Natalia
    Goyal, Akanksha
    Hoffmann, Markus
    Samatova, Ekaterina
    Peske, Frank
    Poehlmann, Stefan
    Rodnina, Marina V.
    NUCLEIC ACIDS RESEARCH, 2019, 47 (10) : 5210 - 5222
  • [4] HIV-1 PROTEASE SPECIFICITY OF PEPTIDE CLEAVAGE IS SUFFICIENT FOR PROCESSING OF GAG AND POL POLYPROTEINS
    DARKE, PL
    NUTT, RF
    BRADY, SF
    GARSKY, VM
    CICCARONE, TM
    LEU, CT
    LUMMA, PK
    FREIDINGER, RM
    VEBER, DF
    SIGAL, IS
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 156 (01) : 297 - 303
  • [5] A comparison of gag-pol precursor cleavage in naturally arising HIV variants
    Bloom, G
    Perez, E
    Parikh, S
    Kay, J
    Mills, J
    Goodenow, M
    Dunn, BM
    ASPARTIC PROTEINASES: RETROVIRAL AND CELLULAR ENZYMES, 1998, 436 : 53 - 57
  • [6] CHARACTERIZATION OF RIBOSOMAL FRAMESHIFTING IN HIV-1 GAG-POL EXPRESSION
    JACKS, T
    POWER, MD
    MASIARZ, FR
    LUCIW, PA
    BARR, PJ
    VARMUS, HE
    NATURE, 1988, 331 (6153) : 280 - 283
  • [7] Persistence of processed HIV-1 Gag and Gag-Pol proteins following treatment with HIV-1 protease inhibitors.
    Speck, RR
    Yu, XF
    Flexner, C
    FASEB JOURNAL, 2000, 14 (04): : A185 - A185
  • [8] Subcellular Localization of HIV-1 gag-pol mRNAs Regulates Sites of Virion Assembly
    Becker, Jordan T.
    Sherer, Nathan M.
    JOURNAL OF VIROLOGY, 2017, 91 (06)
  • [9] EFFECT OF 2 NOVEL INHIBITORS OF THE HUMAN-IMMUNODEFICIENCY-VIRUS PROTEASE ON THE MATURATION OF THE HIV GAG AND GAG-POL POLYPROTEINS
    OVERTON, HA
    MCMILLAN, DJ
    GRIDLEY, SJ
    BRENNER, J
    REDSHAW, S
    MILLS, JS
    VIROLOGY, 1990, 179 (01) : 508 - 511
  • [10] Efavirenz Enhances HIV-1 Gag Processing at the Plasma Membrane through Gag-Pol Dimerization
    Sudo, Sho
    Haraguchi, Hiyori
    Hirai, Yoko
    Gatanaga, Hiroyuki
    Sakuragi, Jun-ichi
    Momose, Fumitaka
    Morikawa, Yuko
    JOURNAL OF VIROLOGY, 2013, 87 (06) : 3348 - 3360