Polar Group Burial Contributes More to Protein Stability than Nonpolar Group Burial
- 14 December 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 40 (2) , 310-313
- https://doi.org/10.1021/bi001574j
Abstract
On the basis of studies of Asn to Ala mutants, the gain in stability from burying amide groups that are hydrogen bonded to peptide groups is 80 cal/(mol Å3). On the basis of similar studies of Leu to Ala and Ile to Val mutants, the gain in stability from burying −CH2− groups is 50 cal/(mol Å3). Thus, the burial of an amide group contributes more to protein stability than the burial of an equivalent volume of −CH2− groups. Applying these results to folded proteins leads to the surprising conclusion that peptide group burial makes a larger contribution to protein stability than nonpolar side chain burial. Several studies have shown that the desolvation penalty for burying peptide groups is considerably smaller than generally thought. This suggests that the hydrogen bonding and van der Waals interactions of peptide groups in the tightly packed interior of folded protein are more favorable than similar interactions with water in the unfolded protein.Keywords
This publication has 9 references indexed in Scilit:
- Protein packing: dependence on protein size, secondary structure and amino acid compositionJournal of Molecular Biology, 2000
- Protein folding: from the levinthal paradox to structure predictionJournal of Molecular Biology, 1999
- The packing density in proteins: standard radii and volumes 1 1Edited by J. M. ThorntonJournal of Molecular Biology, 1999
- Native proteins are surface-molten solids: application of the lindemann criterion for the solid versus liquid state 1 1Edited by A. R. FershtJournal of Molecular Biology, 1999
- Hydrogen bonding stabilizes globular proteinsBiophysical Journal, 1996
- Satisfying Hydrogen Bonding Potential in ProteinsJournal of Molecular Biology, 1994
- Contribution of Hydration to Protein Folding ThermodynamicsJournal of Molecular Biology, 1993
- On the nature of the protein interiorBiochimica et Biophysica Acta (BBA) - Protein Structure, 1971
- The general theory of molecular forcesTransactions of the Faraday Society, 1937