7z3t
From Proteopedia
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7z3t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7z3t OCA], [https://pdbe.org/7z3t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7z3t RCSB], [https://www.ebi.ac.uk/pdbsum/7z3t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7z3t ProSAT]</span></td></tr> | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7z3t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7z3t OCA], [https://pdbe.org/7z3t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7z3t RCSB], [https://www.ebi.ac.uk/pdbsum/7z3t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7z3t ProSAT]</span></td></tr> | ||
</table> | </table> | ||
- | == | + | <div style="background-color:#fffaf0;"> |
- | + | == Publication Abstract from PubMed == | |
+ | Several drug screening campaigns identified Calpeptin as a drug candidate against SARS-CoV-2. Initially reported to target the viral main protease (M(pro)), its moderate activity in M(pro) inhibition assays hints at a second target. Indeed, we show that Calpeptin is an extremely potent cysteine cathepsin inhibitor, a finding additionally supported by X-ray crystallography. Cell infection assays proved Calpeptin's efficacy against SARS-CoV-2. Treatment of SARS-CoV-2-infected Golden Syrian hamsters with sulfonated Calpeptin at a dose of 1 mg/kg body weight reduces the viral load in the trachea. Despite a higher risk of side effects, an intrinsic advantage in targeting host proteins is their mutational stability in contrast to highly mutable viral targets. Here we show that the inhibition of cathepsins, a protein family of the host organism, by calpeptin is a promising approach for the treatment of SARS-CoV-2 and potentially other viral infections. | ||
+ | |||
+ | Calpeptin is a potent cathepsin inhibitor and drug candidate for SARS-CoV-2 infections.,Reinke PYA, de Souza EE, Gunther S, Falke S, Lieske J, Ewert W, Loboda J, Herrmann A, Rahmani Mashhour A, Karnicar K, Usenik A, Lindic N, Sekirnik A, Botosso VF, Santelli GMM, Kapronezai J, de Araujo MV, Silva-Pereira TT, Filho AFS, Tavares MS, Florez-Alvarez L, de Oliveira DBL, Durigon EL, Giaretta PR, Heinemann MB, Hauser M, Seychell B, Bohler H, Rut W, Drag M, Beck T, Cox R, Chapman HN, Betzel C, Brehm W, Hinrichs W, Ebert G, Latham SL, Guimaraes AMS, Turk D, Wrenger C, Meents A Commun Biol. 2023 Oct 18;6(1):1058. doi: 10.1038/s42003-023-05317-9. PMID:37853179<ref>PMID:37853179</ref> | ||
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+ | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
+ | </div> | ||
+ | <div class="pdbe-citations 7z3t" style="background-color:#fffaf0;"></div> | ||
+ | == References == | ||
+ | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> |
Current revision
Crystal structure of apo human Cathepsin L
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Categories: Homo sapiens | Large Structures | Beck T | Boehler H | Chapman HN | Cox R | Ewert W | Falke S | Guenther S | Hauser M | Hinrichs W | Karnicar K | Lach M | Lieske J | Lindic N | Loboda J | Meents A | Rahmani Mashhour A | Reinke PYA | Turk D | Usenik A