Modelling of poliovirus. HIV-1 antigen chimaeras

M J Crabbe, D J Evans, J W Almond

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

We have used laboratory-based molecular modelling to identify structural features of antigen chimaeras of poliovirus expressing epitopes from human immunodeficiency virus (HIV-1) that may affect virus viability. Chimaeras were constructed by replacement of antigenic site 1 of VP1 by sequences corresponding to epitopes from HIV-1. Loop volume, estimated by approximating the loop to an ellipsoid was significantly (P less than 0.001) lower in viable (2062.1 A3 +/- 400.2) than in non-viable (3617 A3 +/- 650.7) constructs. Our results suggest that viable virus will only be formed when antigen chimeras modified at antigenic site of VP1 have a loop occupying a similar volume in space to that occupied by the antigenic site 1 loop. In addition, the modified loop must fit with the peptide bond angles and distances at the top of the beta-barrel of VP1.
Original languageEnglish
Pages (from-to)194-8
Number of pages5
JournalFEBS Letters
Volume271
Issue number1-2
Publication statusPublished - 1 Oct 1990

Keywords

  • Amino Acid Sequence
  • Chimera
  • Computer Simulation
  • Epitopes
  • HIV Antigens
  • HIV-1
  • Models, Molecular
  • Molecular Sequence Data
  • Poliovirus
  • Protein Conformation
  • Solubility

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