Validation of molecular force field parameters for peptides including isomerized amino acids. Issue 4 (2nd February 2018)

• Record Type: Journal Article
• Authors: Oda, Akifumi; Nakayoshi, Tomoki; Fukuyoshi, Shuichi; Kurimoto, Eiji; Yamaotsu, Noriyuki; Hirono, Shuichi; Takahashi, Ohgi
• Is Part Of: Chirality. Volume 30:Issue 4(2018)
• Page Start: 332
• Page End: 341
• Publication Date: 2018-02-02
• Subjects: d‐amino acid -- density functional theory -- force field -- molecular mechanics -- β‐amino acid; Chirality -- Periodicals; Pharmaceutical chemistry -- Periodicals; 541.22
• DOI: 10.1002/chir.22821
• Languages: English
• ISSNs: 0899-0042

Abstract

Abstract: Recently, stereoinversions and isomerizations of amino acid residues in the proteins of living beings have been observed. Because isomerized amino acids cause structural changes and denaturation of proteins, isomerizations of amino acid residues are suspected to cause age‐related diseases. In this study, AMBER molecular force field parameters were tested by using computationally generated nonapeptides and tripeptides including stereoinverted and/or isomerized amino acid residues. Energy calculations by using density functional theory were also performed for comparison. Although the force field parameters were developed by parameter fitting forl ‐α‐amino acids, the accuracy of the computational results ford ‐amino acids and β‐amino acids was comparable to those forl ‐α‐amino acids. The conformational energies for tripeptides calculated by using density functional theory were reproduced more accurately than those for nonapeptides calculated by using the molecular mechanical force field. The evaluations were performed for the ff99SB, ff03, ff12SB, and the latest ff14SB force field parameters. Abstract :