The increased availability of sequences raises the need for sequence to reactivity algorithms, SRA, which quantitatively predict the reactivity of members of a family of proteins from their sequence alone. An algorithm for predicting the standard free energies of association between six selected serine proteinases and a large subset of Kazal family inhibitors was just developed in our laboratory. It was tested by comparing its predictions to already known results for 92 natural avian ovomucoid third domains and on five other, quite unrelated, Kazal family inhibitors. The SRA allows us to predict the best possible, most specific possible and least specific possible sequences for the six enzymes. We plan to express these and test them as an additional important test. Numerous other design objectives are possible. This should be highly useful in drug design either directly as proteins or as models for peptidomimetics. The SRA is additivity based and the tests confirm that additivity holds very well for most residue pairs. However, the pair P2 and P1' is a clear exception and at this time, we cannot predict for pairs that we did not measure. We propose to remove this restriction thus greatly widening the SRA. A number of other restrictions will also be eliminated. The SRA will be more useful to biologists when it is extended to more enzymes. Additivity within a family is called intrascaffolding additivity. Additivity between families is called as interscaffolding additivity and will continue to be studied. Aside from the standard free energy of association, the enthalpy, entropy, heat capacity change, the on and off rate constants, the pH dependence and the equilibrium constant for the reactive site peptide bond hydrolysis are expected to be largely additive. These will be studied on the existing variant set. About 10 percent of the cases tested are nonadditive. These will be selected for detailed study with the aim of elucidating how additivity fails and incorporating corrections into the SRA for such failures. It is anticipated that the ability to correct will be even more important when defining SRAs for other less additive systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM063539-01
Application #
6359277
Study Section
Molecular and Cellular Biophysics Study Section (BBCA)
Program Officer
Flicker, Paula F
Project Start
2001-06-01
Project End
2005-05-31
Budget Start
2001-06-01
Budget End
2002-05-31
Support Year
1
Fiscal Year
2001
Total Cost
$459,242
Indirect Cost
Name
Purdue University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
072051394
City
West Lafayette
State
IN
Country
United States
Zip Code
47907
Qasim, Mohammad A; Wang, Lixia; Qasim, Sabiha et al. (2013) Additivity-based design of the strongest possible turkey ovomucoid third domain inhibitors for porcine pancreatic elastase (PPE) and Streptomyces griseus protease B (SGPB). FEBS Lett 587:3021-6
Qasim, Mohammad A; Song, Jikui; Markley, John L et al. (2010) Cleavage of peptide bonds bearing ionizable amino acids at P(1) by serine proteases with hydrophobic S(1) pocket. Biochem Biophys Res Commun 400:507-10
Yi, Zhengping; Vitek, Olga; Qasim, M A et al. (2006) Functional evolution within a protein superfamily. Proteins 63:697-708
Kelly, Clyde A; Laskowski Jr, Michael; Qasim, M A (2005) The role of scaffolding in standard mechanism serine proteinase inhibitors. Protein Pept Lett 12:465-71
Qasim, M A (2005) From the discovery of the reactive site of inhibitors to their sequence to reactivity algorithm. Protein Pept Lett 12:397-401
Li, Jiangtian; Yi, ZhengPing; Laskowski, Michael C et al. (2005) Analysis of sequence-reactivity space for protein-protein interactions. Proteins 58:661-71
Maynes, Jason T; Cherney, Maia M; Qasim, M A et al. (2005) Structure of the subtilisin Carlsberg-OMTKY3 complex reveals two different ovomucoid conformations. Acta Crystallogr D Biol Crystallogr 61:580-8
Newton, Kelly A; Pitteri, Sharon J; Laskowski Jr, Michael et al. (2004) Effects of single amino acid substitution on the collision-induced dissociation of intact protein ions: Turkey ovomucoid third domain. J Proteome Res 3:1033-41
Suzuki, Noriko; Laskowski Jr, Michael; Lee, Yuan C (2004) Phylogenetic expression of Galalpha1-4Gal on avian glycoproteins: glycan differentiation inscribed in the early history of modern birds. Proc Natl Acad Sci U S A 101:9023-8
Song, Jikui; Laskowski Jr, Michael; Qasim, M A et al. (2003) NMR determination of pKa values for Asp, Glu, His, and Lys mutants at each variable contiguous enzyme-inhibitor contact position of the turkey ovomucoid third domain. Biochemistry 42:2847-56

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