Catalysis of cis/trans isomerization in native HIV-1 capsid by human cyclophilin A

Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5247-52. doi: 10.1073/pnas.082100499. Epub 2002 Apr 2.

Abstract

Packaging of cyclophilin A (CypA) into HIV-1 virions is essential for efficient replication; however, the reason for this is unknown. Incorporation is mediated through binding to the Gly-89-Pro-90 peptide bond of the N-terminal domain of HIV-1 capsid (CA(N)). Despite the fact that CypA is a peptidyl-prolyl cis/trans isomerase, catalytic activity on CA(N) has not been observed previously. We show here, using NMR exchange spectroscopy, that CypA does not only bind to CA(N) but also catalyzes efficiently the cis/trans isomerization of the Gly-89-Pro-90 peptide bond. In addition, conformational changes in CA(N) distal to the CypA binding loop are observed on CypA binding and catalysis. The results provide experimental evidence for efficient CypA catalysis on a natively folded and biologically relevant protein substrate.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Capsid / chemistry*
  • Catalysis
  • Crystallography, X-Ray
  • Cyclophilin A / chemistry*
  • Genetic Vectors
  • HIV-1 / chemistry*
  • HIV-1 / pathogenicity
  • Humans
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Models, Chemical
  • Models, Molecular
  • Peptides / chemistry
  • Protein Binding
  • Protein Conformation
  • Protein Folding
  • Protein Structure, Tertiary
  • Stereoisomerism
  • Virulence

Substances

  • Peptides
  • Cyclophilin A