J Biol Chem, Vol. 273, Issue 44, 28759-28765, October 30, 1998

New Synthetic Non-peptide Ligands for Classical Major Histocompatibility Complex Class I Molecules

Alberto Bianco, Carsten Brock^¶, Claus Zabel^¶, Tilmann Walk, Peter Walden^¶, and Günther Jung

From the  Institut für Organische Chemie, Universität Tübingen, D-72076 Tübingen, Germany and the ^¶ Dermatologische Klinik, Charité, Humboldt-Universität, D-10089 Berlin, Germany

Poly-N-acylated amines, as a new class of synthetic non-peptide ligands for the murine major histocompatibility complex (MHC) class I molecule H-2K^b, were developed on the basis of the ovalbumin-derived peptide epitope SIINFEKL. Non-peptidic structural elements were introduced at the C-terminal part of the ligand and include the two dominant anchors at positions 5 and 8. Several oligomers and five different combinatorial libraries were synthesized and tested for their H-2K^b-binding capacities in an MHC stabilization assay. First, the optimal spacing and geometry of the side chains were determined using a series of oligomers with different main chain modifications. Then, based on the structure with the highest binding efficiency, randomized libraries were designed that contain 26 different aromatic, heteroaromatic, or pseudoaromatic side chains for the dominant anchor at position 5, which is deeply buried inside the MHC peptide-binding groove and is crucial for the conformational stability of the entire peptide-MHC complex. Similarly, a series of aliphatic side chains were tested for the second dominant anchor at position 8. MHC-binding and MHC-stabilizing oligomers with defined structures were derived from these libraries by deconvolution.