THE ADENOVIRUS PROTEASE IS REQUIRED FOR VIRUS ENTRY INTO HOST-CELLS

被引:85
作者
COTTEN, M [1 ]
WEBER, JM [1 ]
机构
[1] UNIV SHERBROOKE, FAC MED, DEPT MICROBIOL, SHERBROOKE, PQ J1H 5N4, CANADA
关键词
D O I
10.1006/viro.1995.0022
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have analyzed the mechanisms used by adenovirus to gain entry into the host cell. Using both virus infection and the ability of adenovirus particles to enhance polylysine/DNA uptake as a measure of virus entry, we have demonstrated that the adenovirus-encoded 23K protease is required for two functions in the infection process. A proteolytic processing of the capsid is required to generate a Virus capsid that can increase membrane interactions at pH 5. We have found that forms of adenovirus capsid that have not undergone the processing reactions (immature capsids) are deficient in their ability to disrupt membranes at pH 5 and are unable to enhance the entry of polylysine/DNA complexes. A second role of the protease was revealed by experiments using inhibitors of the protease, Mature virus capsids lose their ability to enhance gene delivery and become noninfectious after exposure to inhibitors of the protease (1 mu M N-ethylmaleimide, 100-300 PM copper chloride, 1 mu M MDL28170, or anti-protease antiserum), suggesting that the viral protease activity is required during the cellular entry process. (C) 1995 Academic Press. Inc.
引用
收藏
页码:494 / 502
页数:9
相关论文
共 47 条
[1]   THE PROTEINASE POLYPEPTIDE OF ADENOVIRUS SEROTYPE-2 VIRIONS [J].
ANDERSON, CW .
VIROLOGY, 1990, 177 (01) :259-272
[2]   CONDENSATION OF DNA BY TRIVALENT CATIONS .1. EFFECTS OF DNA LENGTH AND TOPOLOGY ON THE SIZE AND SHAPE OF CONDENSED PARTICLES [J].
ARSCOTT, PG ;
LI, AZ ;
BLOOMFIELD, VA .
BIOPOLYMERS, 1990, 30 (5-6) :619-630
[3]  
Berne B. J., 1990, DYNAMIC LIGHT SCATTE
[4]   PH-DEPENDENT LYSIS OF LIPOSOMES BY ADENOVIRUS [J].
BLUMENTHAL, R ;
SETH, P ;
WILLINGHAM, MC ;
PASTAN, I .
BIOCHEMISTRY, 1986, 25 (08) :2231-2237
[5]   REDUNDANT CONTROL OF ADENOVIRUS LATE GENE-EXPRESSION BY EARLY REGION-4 [J].
BRIDGE, E ;
KETNER, G .
JOURNAL OF VIROLOGY, 1989, 63 (02) :631-638
[6]   THE ADENOVIRUS L3 23-KILODALTON PROTEINASE CLEAVES THE AMINO-TERMINAL HEAD DOMAIN FROM CYTOKERATIN 18 AND DISRUPTS THE CYTOKERATIN NETWORK OF HELA-CELLS [J].
CHEN, PH ;
ORNELLES, DA ;
SHENK, T .
JOURNAL OF VIROLOGY, 1993, 67 (06) :3507-3514
[7]   HUMAN ADENOVIRUS-2 TEMPERATURE-SENSITIVE MUTANT-112 CONTAINS 3 MUTATIONS IN THE PROTEIN-IIIA GENE [J].
CHROBOCZEK, J ;
VIARD, F ;
DHALLUIN, JC .
GENE, 1986, 49 (01) :157-160
[8]   PSORALEN TREATMENT OF ADENOVIRUS PARTICLES ELIMINATES VIRUS-REPLICATION AND TRANSCRIPTION WHILE MAINTAINING THE ENDOSOMOLYTIC ACTIVITY OF THE VIRUS CAPSID [J].
COTTEN, M ;
SALTIK, M ;
KURSA, M ;
WAGNER, E ;
MAASS, G ;
BIRNSTIEL, ML .
VIROLOGY, 1994, 205 (01) :254-261
[9]   CHICKEN ADENOVIRUS (CELO VIRUS) PARTICLES AUGMENT RECEPTOR-MEDIATED DNA DELIVERY TO MAMMALIAN-CELLS AND YIELD EXCEPTIONAL LEVELS OF STABLE TRANSFORMANTS [J].
COTTEN, M ;
WAGNER, E ;
ZATLOUKAL, K ;
BIRNSTIEL, ML .
JOURNAL OF VIROLOGY, 1993, 67 (07) :3777-3785
[10]  
COTTEN M, 1993, METHOD ENZYMOL, V217, P618