Capsid assembly in a family of animal viruses primes an autoproteolytic maturation that depends on a single aspartic acid residue.
Capsid assembly in a family of animal viruses primes an autoproteolytic maturation that depends on a single aspartic acid residue.
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DOI:
10.1016/s0021-9258(17)36883-7
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发表时间:
1994-05
期刊:
影响因子:
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通讯作者:
A. Zlotnick;V. Reddy;R. Dasgupta;A. Schneemann;W. Ray;R. Rueckert;J. Johnson
中科院分区:
文献类型:
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作者:
A. Zlotnick;V. Reddy;R. Dasgupta;A. Schneemann;W. Ray;R. Rueckert;J. Johnson
Maturation of noninfectious nodavirus provirions occurs by autoproteolytic cleavage of most of the 180 copies of the alpha-protein that make up the icosahedral capsid. This maturation, which is much slower than viral assembly, produces an infectious particle that is more stable than the provirion and makes viral uncoating thermodynamically distinct from assembly, allowing assembly and (a time-delayed) uncoating to occur under similar conditions. The results of structural, computational, and molecular genetic studies suggest that maturation depends both on intrasubunit strain, produced during assembly, and on a critical aspartic acid residue. This residue lies in a hydrophobic pocket that is stabilized by intersubunit contacts. It is close to the scissile bond and exhibits an environmentally elevated pKa. The apparent involvement of a single acidic residue in the hydrolytic cleavage of a peptide bond contrasts with the involvement of 2 such residues in acid proteases.