Literature DB >> 12488001

Relation between peptide backbone solvation and the energetics of peptide hydrogen bonds.

Robert L Baldwin1.   

Abstract

The H-bond inventory approach is used commonly to interpret data involving changes in the number or types of protein hydrogen bonds. I point out here that this approach gives an incorrect answer either for the standard free energy or enthalpy of the reaction between simple amides and water. On the other hand, an electrostatic solvation approach fits almost within error the polar solvation free energies of small molecules, including amides. The electrostatic solvation approach is used here to discuss the relation between peptide backbone solvation and the enthalpy change for forming an alanine helix. Copyright 2002 Elsevier Science B.V.

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Year:  2002        PMID: 12488001     DOI: 10.1016/s0301-4622(02)00195-3

Source DB:  PubMed          Journal:  Biophys Chem        ISSN: 0301-4622            Impact factor:   2.352


  3 in total

Review 1.  Protein-solvent interactions.

Authors:  Ninad Prabhu; Kim Sharp
Journal:  Chem Rev       Date:  2006-05       Impact factor: 60.622

2.  H-Bonding network in fully deuterated N-methylformamide-water mixtures as studied by neutron scattering. Complementarity to X-ray study.

Authors:  Abir Chebaane; Ferid Hammami; Salah Nasr; Mohamed Bahri; Marie-Claire Bellissent-Funel
Journal:  Eur Phys J E Soft Matter       Date:  2015-01-29       Impact factor: 1.890

3.  Energetics and structure of alanine-rich α-helices via adaptive steered molecular dynamics.

Authors:  Yi Zhuang; Hailey R Bureau; Christine Lopez; Ryan Bucher; Stephen Quirk; Rigoberto Hernandez
Journal:  Biophys J       Date:  2021-03-26       Impact factor: 4.033

  3 in total

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