Human cytomegalovirus virion proteins

被引:59
作者
Britt, WJ
Boppana, S
机构
[1] Univ Alabama Birmingham, Sch Med, Dept Pediat, Birmingham, AL USA
[2] Univ Alabama Birmingham, Sch Med, Dept Microbiol, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Sch Med, Dept Neurobiol, Birmingham, AL USA
关键词
human cytomegalovirus; virion structural proteins; viron proteins;
D O I
10.1016/j.humimm.2004.02.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Human cytomegalovirus (HCMV) is the largest member of the family of human herpesviruses. The number of virus encoded proteins and the complexity of their functions in the life cycle of this virus are reflected in the size of its genome. There continues to be some controversy surrounding the exact protein coding capacity of the virus with estimates ranging from 160 open reading frames to more than 200 open reading frames. Very recent studies using mass spectrometry to determine the viral proteome suggests that the number of viral proteins may be even greater than previous estimates. The proteins of the virion capsid have readily identifiable homologous proteins in the capsid of the more extensively studied herpes simplex virus, likely because of similar capsid structure and assembly pathways. In contrast, the tegument and the envelope of HCMV contain a significant number of proteins that lack structural homology to proteins found in either a or gamma-herpesviruses. This brief overview discusses some of the general features and possible functions of the HCMV virion structural proteins in the replicative cycle of this virus. Human Immunology 65, 395-402 (2004). (C) American Society for Histocompatibility and Immunogenetics, 2004. Published by Elsevier Inc.
引用
收藏
页码:395 / 402
页数:8
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