Targeting Gαi/s Proteins with Peptidyl Nucleotide Exchange Modulators
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...
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Veröffentlicht in: | ACS chemical biology 2022-02, Vol.17 (2), p.463-473 |
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creator | Nubbemeyer, Britta Paul George, Ajay Abisheck Kühl, Toni Pepanian, Anna Beck, Maximilian Steve Maghraby, Rahma Shetab Boushehri, Maryam Muehlhaupt, Maximilian Pfeil, Eva Marie Annala, Suvi Katariina Ammer, Hermann Imhof, Diana Pei, Dehua |
description | 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. |
doi_str_mv | 10.1021/acschembio.1c00929 |
format | Article |
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Biol</addtitle><description>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. 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Biol</addtitle><date>2022-02-18</date><risdate>2022</risdate><volume>17</volume><issue>2</issue><spage>463</spage><epage>473</epage><pages>463-473</pages><issn>1554-8929</issn><eissn>1554-8937</eissn><abstract>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. 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subjects | Heterotrimeric GTP-Binding Proteins - metabolism Heterotrimeric GTP-Binding Proteins - pharmacology Molecular Docking Simulation Nucleotides - metabolism Peptides - chemistry Signal Transduction |
title | Targeting Gαi/s Proteins with Peptidyl Nucleotide Exchange Modulators |
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