4.6 Article

Three-dimensional localization of the smallest capsid protein in the human cytomegalovirus capsid

Journal

JOURNAL OF VIROLOGY
Volume 79, Issue 2, Pages 1327-1332

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.79.2.1327-1332.2005

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Funding

  1. NATIONAL CENTER FOR RESEARCH RESOURCES [P41RR002250] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI046420, R01AI035602] Funding Source: NIH RePORTER
  3. NCRR NIH HHS [P41 RR002250, P41RR02250] Funding Source: Medline
  4. NIAID NIH HHS [R01 AI035602, R01 AI046420, AI35602, AI46420] Funding Source: Medline

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The smallest capsid proteins (SCPs) of the human herpesviruses differ substantially in size and sequence and are thought to impart some unique aspects of infection to their respective viruses. We used electron cryomicroscopy and antibody labeling to show that the 8-kDa SCP of human cytomegalovirus is attached only to major capsid protein subunits of the hexons, not the pentons. Thus, the SCPs of different herpesviruses illustrate that a protein can evolve significantly in sequence, structure, and function, while preserving its role in the architecture of the virus by binding to a specific partner in a specific oligomeric state.

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