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Proceedings of the National Academy of Sciences of the United States of America|November 20, 2025
Structural basis of modified ligand selectivity from N-terminal PAC1R alternative splicingJessica J Lu, Giuseppe Deganutti, Miaomiao Li, et al.Biochemical Pharmacology|March 29, 2020
Rational development of a high-affinity secretin receptor antagonistMaoqing Dong, Kaleeckal G Harikumar, Sweta R Raval, et al.Science (New York, N.Y.)|February 19, 2021
Structure and dynamics of the CGRP receptor in apo and peptide-bound formsTracy M Josephs, Matthew J Belousoff, Yi-Lynn Liang, et al.European Journal of Pharmacology|April 14, 2018
Vascular and molecular pharmacology of the metabolically stable CGRP analogue, SAXMajid Sheykhzade, Bahareh Abdolalizadeh, Cassandra Koole, et al.Journal of the American Chemical Society|August 17, 2019
O-GlcNAc Engineering of GPCR Peptide-Agonists Improves Their Stability and in Vivo ActivityPaul M Levine, Aaron T Balana, Emmanuel Sturchler, et al.Biochemical Pharmacology|August 2, 2021
Insights into agonist-elicited activation of the human glucose-dependent insulinotropic polypeptide receptorElita Yuliantie, Wijnand J C van der Velden, Viktorija Labroska, et al.Plos Biology|June 4, 2021
Structures of the human cholecystokinin 1 (CCK1) receptor bound to Gs and Gq mimetic proteins provide insight into mechanisms of G protein selectivityJesse I Mobbs, Matthew J Belousoff, Kaleeckal G Harikumar, et al.Nature Chemical Biology|August 3, 2023
Structural insight into selectivity of amylin and calcitonin receptor agonistsJianjun Cao, Matthew J Belousoff, Elliot Gerrard, et al.Molecular Cell|February 1, 2020
Toward a Structural Understanding of Class B GPCR Peptide Binding and ActivationYi-Lynn Liang, Matthew J Belousoff, Peishen Zhao, et al.Bioconjugate Chemistry|May 16, 2023
Glycosylation Improves the Proteolytic Stability of ExenatideChaitra Chandrashekar, Yuji Nishiuchi, Barbara Fam White, et al.Pageof 12