Flexibility of Amino Acid Residues at Position Four of Nonapeptides Enhances Their Binding to Human Leucocyte Antigen (HLA) Molecules

The binding affinity of synthetic nonapeptides to human leucocyte antigens (HLA) molecules of the A0201 allotype, the most common in Caucasian, is enhanced or reduced by suitable amino acid substitutions at position 4, as a result of increased or decreased chain flexibility. A higher flexibility of...

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Veröffentlicht in:Zeitschrift für Naturforschung C. A journal of biosciences 2000-01, Vol.55 (1), p.109-114
Hauptverfasser: Chersi, Alberto, Modugno, Francesca di, Rosano, Laura
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Modugno, Francesca di
Rosano, Laura
description The binding affinity of synthetic nonapeptides to human leucocyte antigens (HLA) molecules of the A0201 allotype, the most common in Caucasian, is enhanced or reduced by suitable amino acid substitutions at position 4, as a result of increased or decreased chain flexibility. A higher flexibility of the bond at this position correlates with an easier accomodation of the fragment into the HLA groove, while rigidity of the peptide chain appears to interfere. These data are based on two lines of evidence: a) most natural high affnity ligands for HLA-A0201 possess, at position 4, flexible residues b) substitutions of such residues by rigid amino acids results in a decrease of binding affinity.
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subjects Amino Acid Sequence
Binding Sites
European Continental Ancestry Group
HLA-A Antigens - chemistry
Human Leucocyte Antigen (HLA)
Humans
Kinetics
Oligopeptides - chemistry
Peptide Binding
Protein Conformation
Secondary Interactions
title Flexibility of Amino Acid Residues at Position Four of Nonapeptides Enhances Their Binding to Human Leucocyte Antigen (HLA) Molecules
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