Title

Evaluation of the substrate envelope hypothesis for inhibitors of HIV-1 protease

UMMS Affiliation

Department of Biochemistry and Molecular Pharmacology

Publication Date

2007-05-03

Document Type

Article

Subjects

Binding Sites; Crystallography, X-Ray; HIV Protease; HIV Protease Inhibitors; HIV-1; Kinetics; Models, Molecular; Molecular Conformation; Mutation; Recombinant Proteins; Substrate Specificity

Disciplines

Biochemistry, Biophysics, and Structural Biology | Pharmacology, Toxicology and Environmental Health

Abstract

Crystallographic data show that various substrates of HIV protease occupy a remarkably uniform region within the binding site; this region has been termed the substrate envelope. It has been suggested that an inhibitor that fits within the substrate envelope should tend to evade viral resistance because a protease mutation that reduces the affinity of the inhibitor will also tend to reduce the affinity of substrate, and will hence decrease the activity of the enzyme. Accordingly, inhibitors that fit the substrate envelope better should be less susceptible to clinically observed resistant mutations, since these must also allow substrates to bind. The present study describes a quantitative measure of the volume of a bound inhibitor falling outside the substrate envelope, and observes that this quantity correlates with the inhibitor's losses in affinity to clinically relevant mutants. This measure may thus be useful as a penalty function in the design of robust HIV protease inhibitors.

DOI of Published Version

10.1002/prot.21431

Source

Proteins. 2007 Aug 1;68(2):561-7. Link to article on publisher's site

Journal/Book/Conference Title

Proteins

Related Resources

Link to Article in PubMed

PubMed ID

17474129

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