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. 1989 Feb;86(3):807–811. doi: 10.1073/pnas.86.3.807

Activity of purified biosynthetic proteinase of human immunodeficiency virus on natural substrates and synthetic peptides.

H G Kräusslich 1, R H Ingraham 1, M T Skoog 1, E Wimmer 1, P V Pallai 1, C A Carter 1
PMCID: PMC286566  PMID: 2644644

Abstract

Retroviral capsid proteins and replication enzymes are synthesized as polyproteins that are proteolytically processed to the mature products by a virus-encoded proteinase. We have purified the proteinase of human immunodeficiency virus (HIV), expressed in Escherichia coli, to approximately 90% purity. The purified enzyme at a concentration of approximately 20 nM gave rapid, efficient, and specific cleavage of an in vitro synthesized gag precursor protein. Purified HIV proteinase also induced specific cleavage of five decapeptide substrates whose amino acid sequences corresponded to cleavage sites in the HIV polyprotein but not of a peptide corresponding to a cleavage site in another retrovirus. Competition experiments with different peptides allowed a ranking of cleavage sites. Inhibition studies indicated that the HIV proteinase was inhibited by pepstatin A with an IC50 of 0.7 microM.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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