| Literature DB >> 26602187 |
Krzysztof M Zak1, Radoslaw Kitel2, Sara Przetocka1, Przemyslaw Golik1, Katarzyna Guzik3, Bogdan Musielak3, Alexander Dömling4, Grzegorz Dubin5, Tad A Holak6.
Abstract
Targeting the PD-1/PD-L1 immunologic checkpoint with monoclonal antibodies has recently provided breakthrough progress in the treatment of melanoma, non-small cell lung cancer, and other types of cancer. Small-molecule drugs interfering with this pathway are highly awaited, but their development is hindered by insufficient structural information. This study reveals the molecular details of the human PD-1/PD-L1 interaction based on an X-ray structure of the complex. First, it is shown that the ligand binding to human PD-1 is associated with significant plasticity within the receptor. Second, a detailed molecular map of the interaction surface is provided, allowing definition of the regions within both interacting partners that may likely be targeted by small molecules.Entities:
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Year: 2015 PMID: 26602187 PMCID: PMC4752817 DOI: 10.1016/j.str.2015.09.010
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006