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ACS Chem Biol ; 17(2): 463-473, 2022 02 18.
Artigo em Inglês | MEDLINE | ID: mdl-35042325

RESUMO

Chemical probes that specifically modulate the activity of heterotrimeric G proteins provide excellent tools for investigating G protein-mediated cell signaling. Herein, we report a family of selective peptidyl Gαi/s modulators derived from peptide library screening and optimization. Conjugation to a cell-penetrating peptide rendered the peptides cell-permeable and biologically active in cell-based assays. The peptides exhibit potent guanine-nucleotide exchange modulator-like activity toward Gαi and Gαs. Molecular docking and dynamic simulations revealed the molecular basis of the protein-ligand interactions and their effects on GDP binding. This study demonstrates the feasibility of developing direct Gαi/s modulators and provides a novel chemical probe for investigating cell signaling through GPCRs/G proteins.


Assuntos
Proteínas Heterotriméricas de Ligação ao GTP , Nucleotídeos , Proteínas Heterotriméricas de Ligação ao GTP/metabolismo , Proteínas Heterotriméricas de Ligação ao GTP/farmacologia , Simulação de Acoplamento Molecular , Nucleotídeos/metabolismo , Peptídeos/química , Transdução de Sinais
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