作者: O. P. Zhirnov , T. E. Konakova , W. Garten , H.-D. Klenk
DOI: 10.1128/JVI.73.12.10158-10163.1999
关键词: Oligopeptide 、 Influenza A virus 、 Apoptosis 、 Biology 、 Cleavage (embryo) 、 Virology 、 Caspase 、 Peptide sequence 、 Virus 、 Antibody 、 Molecular biology
摘要: The nucleocapsid protein (NP) (56 kDa) of human influenza A viruses is cleaved in infected cells into a 53-kDa form. Likewise, B virus NP (64 55-kDa with 62-kDa intermediate (O. P. Zhirnov and A. G. Bukrinskaya, Virology 109:174–179, 1981). We show now that an antibody specific for the N terminus reacted uncleaved 56-kDa form but not truncated NP53 form, indicating removal 3-kDa peptide from terminus. Amino acid sequencing revealed cleavage sites ETD16*G A/Aichi/68 DID7*G EAD61*V B/Hong Kong/72 NP. With D at position −1, acidic amino acids −3, aliphatic ones positions −2 +1, recognition motif typical caspases, key enzymes apoptosis. These caspase demonstrated evolutionary stability were retained NPs all viruses. avian viruses, which cells, contains G instead 16. Oligopeptide DEVD derivatives, inhibitors, shown to prevent intracellular All three events, cleavage, increase activity, development apoptosis, coincide data suggest exerted by host caspases associated apoptosis late stages infection.