A comparative molecular similarity index analysis (CoMSIA) study identifies an HLA-A2 binding supermotif

J Comput Aided Mol Des. 2002 Aug-Sep;16(8-9):535-44. doi: 10.1023/a:1021917203966.

Abstract

The 3D-QSAR CoMSIA technique was applied to a set of 458 peptides binding to the five most widespread HLA-A2-like alleles: A*0201, A*0202, A*0203, A*0206 and A*6802. Models comprising the main physicochemical properties (steric bulk, electron density, hydrophobicity and hydrogen-bond formation abilities) were obtained with acceptable predictivity (q2 ranged from 0.385 to 0.683). The use of coefficient contour maps allowed an A2-supermotif to be identified based on common favoured and disfavoured areas. The CoMSIA definition for the best HLA-A2 binder is as follows: hydrophobic aromatic amino acid at position 1; hydrophobic bulky side chains at positions 2, 6 and 9; non-hydrogen-bond-forming amino acids at position 3; small aliphatic hydrogen-bond donors at position 4; aliphatic amino acids at position 5; small aliphatic side chains at position 7; and small aliphatic hydrophilic and hydrogen-bond forming amino acids at position 8.

Publication types

  • Comparative Study

MeSH terms

  • Alleles
  • Amino Acid Motifs
  • Binding Sites
  • Chemical Phenomena
  • Chemistry, Physical
  • Computer Simulation
  • HLA-A Antigens / chemistry
  • HLA-A Antigens / genetics
  • HLA-A Antigens / metabolism
  • HLA-A2 Antigen / chemistry*
  • HLA-A2 Antigen / genetics
  • HLA-A2 Antigen / metabolism*
  • Humans
  • Hydrogen Bonding
  • Hydrophobic and Hydrophilic Interactions
  • In Vitro Techniques
  • Models, Molecular
  • Oligopeptides / chemistry*
  • Oligopeptides / metabolism*
  • Protein Binding
  • Protein Conformation
  • Quantitative Structure-Activity Relationship
  • Static Electricity

Substances

  • HLA-A Antigens
  • HLA-A*02:01 antigen
  • HLA-A2 Antigen
  • Oligopeptides