Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5416517 | Journal of Molecular Structure: THEOCHEM | 2010 | 6 Pages |
Abstract
Computation of accurate intramolecular hydrogen-bonding energies in proteins and peptides is of great importance in understanding the conformational stabilities of peptides and developing a more accurate force field for proteins. In this paper, we apply the analytic potential energy function we proposed previously to estimate the intramolecular hydrogen-bonding energies in α-peptide and β-peptide conformers. The scheme is validated by applying it to four α-peptides and nine β-peptides. The estimated intramolecular hydrogen-bonding energies are in good agreement with those calculated by substitution method. The dipole-dipole interaction of the intramolecular N-Hâ¦OC hydrogen bond lie in the range of 6-8 kcal/mol and the dipole-dipole interaction of the Cα-Hâ¦OC hydrogen bond lie in the range of 1.5-1.8 kcal/mol. All of the results demonstrate that our scheme can simply and quickly yield reasonably correct intramolecular hydrogen-bonding energy in peptides.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Chang-Liang Sun, Chang-Sheng Wang,