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Vol 51(2017) N 3 p. 465-473; DOI 10.1134/S002689331702008X Full Text

A. Cortés1*, J. Coral1, C. McLachlan1, R. Benítez2, L. Pinilla3

Planar molecular arrangements aid the design of MHC class II binding peptides

1Department of Molecular Physics, Synthetic Vaccine and New Drug Research Institute, IVSI, Popayán, Colombia
2Department of Chemistry, Natural Product Chemistry Research Group University of Cauca Popayán, CP 190002 Colombia
3Department of Medicine, Faculty of Medicine National University of Colombia, Bogotá, Colombia

*adrian.cortes205@gmail.com
Received - 2016-04-21; Accepted - 2016-05-19

The coupling between peptides and MHC-II proteins in the human immune system is not well understood. This work presents an evidence-based hypothesis of a guiding intermolecular force present in every human MHC-II protein (HLA-II). Previously, we examined the spatial positions of the fully conserved residues in all HLA-II protein types. In each one, constant planar patterns were revealed. These molecular planes comprise of amino acid groups of the same chemical species (for example, Gly) distributed across the protein structure. Each amino acid plane has a unique direction and this directional element offers spatial selectivity. Constant within all planes, too, is the presence of an aromatic residue possessing electrons in movement, leading the authors to consider that the planes generate electromagnetic fields that could serve as an attractive force in a single direction. Selection and attraction between HLA-II molecules and antigen peptides would, therefore, be non-random, resulting in a coupling mechanism as effective and rapid as is clearly required in the immune response. On the basis of planar projections onto the HLA-II groove, modifications were made by substituting the key residues in the class II-associated invariant chain peptide-a peptide with a universal binding affinity-resulting in eight different modified peptides with affinities greater than that of the unmodified peptide. Accurate and reliable prediction of MHC class II-binding peptides may facilitate the design of universal vaccine-peptides with greatly enhanced binding affinities. The proposed mechanisms of selection, attraction and coupling between HLA-II and antigen peptides are explained further in the paper.

PECC, MHC class II, HLA-II, binding, affinity, CLIP peptide, electromagnetic field



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