Rapid peptide exchange on MHC class I by small molecules elucidates dynamics of bound peptide

Abstract

Complexes of peptides with recombinant major histocompatibility complex class I molecules (rpMHCs) are an important tool for T cell detection, isolation, and activation in cancer immunotherapy. The rapid preparation of rpMHCs is aided by peptide exchange, for which several technologies exist. Here, we show peptide exchange with small-molecule alcohols and demonstrate that they accelerate the dissociation of pre-bound peptides, creating a novel method for rapid production of rpMHCs and increasing the understanding of the conformational flexibility of the MHC-bound peptides.

Keywords

• Peptide exchange
• Small molecule
• Major histocompatibility complex
• MHC class I
• Fluorescence anisotropy
• Nanoscale differential scanning fluorimetry