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Tegument Protein pp150 Sequence-Specific Peptide Blocks Cytomegalovirus Infection.

Abstract
Human cytomegalovirus (HCMV) tegument protein pp150 is essential for the completion of the final steps in virion maturation. Earlier studies indicated that three pp150nt (N-terminal one-third of pp150) conformers cluster on each triplex (Tri1, Tri2A and Tri2B), and extend towards small capsid proteins atop nearby major capsid proteins, forming a net-like layer of tegument densities that enmesh and stabilize HCMV capsids. Based on this atomic detail, we designed several peptides targeting pp150nt. Our data show significant reduction in virus growth upon treatment with one of these peptides (pep-CR2) with an IC50 of 1.33 μM and no significant impact on cell viability. Based on 3D modeling, pep-CR2 specifically interferes with the pp150-capsid binding interface. Cells pre-treated with pep-CR2 and infected with HCMV sequester pp150 in the nucleus, indicating a mechanistic disruption of pp150 loading onto capsids and subsequent nuclear egress. Furthermore, pep-CR2 effectively inhibits mouse cytomegalovirus (MCMV) infection in cell culture, paving the way for future animal testing. Combined, these results indicate that CR2 of pp150 is amenable to targeting by a peptide inhibitor, and can be developed into an effective antiviral.
AuthorsDipanwita Mitra, Mohammad H Hasan, John T Bates, Gene L Bidwell 3rd, Ritesh Tandon
JournalViruses (Viruses) Vol. 13 Issue 11 (11 15 2021) ISSN: 1999-4915 [Electronic] Switzerland
PMID34835083 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Capsid Proteins
  • Phosphoproteins
  • Viral Matrix Proteins
  • pp150 protein, Cytomegalovirus
Topics
  • Animals
  • Capsid
  • Capsid Proteins (metabolism, ultrastructure)
  • Cryoelectron Microscopy (methods)
  • Cytomegalovirus (genetics, metabolism, pathogenicity)
  • Cytomegalovirus Infections (metabolism)
  • Humans
  • Mice
  • Muromegalovirus (metabolism, pathogenicity)
  • Phosphoproteins (metabolism, physiology, ultrastructure)
  • Viral Matrix Proteins (metabolism, physiology, ultrastructure)
  • Virion
  • Virus Assembly

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