Author(s)
O Almog, David Travis Gallagher, Jane E. Ladner, S Strausberg, Patrick Alexander, Phillip Bryan, G L. Gilliland
Abstract
The crystal structures of two thermally stabilized subtilisin BPN' variants, S63 and S88, are reported here at 1.8 and 1.9 resolution, respectively. The micromolar affinity calcium-binding site (site A) has been deleted (δ 75-83) in these variants, enabling the activity and thermostability measurements in chelating conditions. Each of the variants includes mutations known previously to increase the thermostability of calcium independent subtilisin in addition to new stabilizing mutations. S63 has eight amino-acid replacements: D41A, M50F, A73L, Q206W, Y217K, N218S, S221C, and Q271E. S63 has 75-fold greater stability than wild type subtilisin in chelating conditions (10 mM EDTA). The other variant, S88, has ten site-specific changes: Q2K, S3C, P5S, K43N, M50F, A73L, Q206C, Y217K, N218S, and Q271E. The two new cysteines form a disulfide bond, and S88 has 1000 times greater stability than wild type subtilisin in chelating conditions. Comparisons of the two new crystal structures (S63 in space group P21 with cell constants 41.2, 78.1, 36.7, and Β = 114.6 and S88 in space group P212121 with cell constants 54.2 and 60.4, and 82.7) with previous structures of subtilisin BPN reveal the principal changes are in the N-terminal region. The structural basis of the stabilization effects of the new mutations Q2K, S3C, P5S, D41A, Q206C, and Q206W are generally apparent. The effects are attributed to the new disulfide cross-link and to improved hydrophobic packing, new hydrogen bonds, and other rearrangements in the N terminal region.
Citation
Journal of Biological Chemistry
Keywords
calcium-independent, disulfide, enzyme, protein engineering, structure, subtilizin BPN, thermostability
Citation
Almog, O.
, Gallagher, D.
, Ladner, J.
, Strausberg, S.
, Alexander, P.
, Bryan, P.
and Gilliland, G.
(2002),
Structural Basis of Thermostability: Analysis of Stabilizing Mutations in Subtilisin BPN, Journal of Biological Chemistry (Accessed May 15, 2026)
Additional citation formats
Issues
If you have any questions about this publication or are having problems accessing it, please contact [email protected].