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Discovery of pH-Selective Marine and Plant Natural Product Inhibitors of Cathepsin B Revealed by Screening at Acidic and Neutral pH Conditions

[Image: see text] Dysregulation of cathepsin B, which involves the translocation of the enzyme from acidic pH lysosomes to the neutral pH cytosol, followed by the initiation of cell death and inflammation, occurs in numerous brain disorders. The wide difference in the acidic pH (4.6) of lysosomes co...

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Autores principales: Phan, Von V., Mosier, Charles, Yoon, Michael C., Glukhov, Evgenia, Caffrey, Conor R., O’Donoghue, Anthony J., Gerwick, William H., Hook, Vivian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330179/
https://www.ncbi.nlm.nih.gov/pubmed/35910167
http://dx.doi.org/10.1021/acsomega.2c02287
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author Phan, Von V.
Mosier, Charles
Yoon, Michael C.
Glukhov, Evgenia
Caffrey, Conor R.
O’Donoghue, Anthony J.
Gerwick, William H.
Hook, Vivian
author_facet Phan, Von V.
Mosier, Charles
Yoon, Michael C.
Glukhov, Evgenia
Caffrey, Conor R.
O’Donoghue, Anthony J.
Gerwick, William H.
Hook, Vivian
author_sort Phan, Von V.
collection PubMed
description [Image: see text] Dysregulation of cathepsin B, which involves the translocation of the enzyme from acidic pH lysosomes to the neutral pH cytosol, followed by the initiation of cell death and inflammation, occurs in numerous brain disorders. The wide difference in the acidic pH (4.6) of lysosomes compared to the neutral pH (7.2) of the cytosol suggests that screening at different pH conditions may identify pH-selective modulators of cathepsin B. Therefore, a collection of pure marine and plant natural product (NP) compounds, with synthetic compounds, was screened at pH 4.6 and pH 7.2 in cathepsin B assays, which led to the identification of GER-12 (Crossbyanol B) and GER-24 ((7Z,9Z,12Z)-octadeca-7,9,12-trien-5-ynoic acid) marine NP inhibitors at acidic pH but not at neutral pH. GER-12 was effective for the reversible inhibition of cathepsin B, with an IC(50) of 3 μM. GER-24 had an IC(50) of 16 μM and was found to be an irreversible inhibitor. These results show that NP screening at distinct biological pH conditions can lead to the identification of pH-selective cathepsin B modulators. These findings suggest that screening efforts for molecular probes and drug discovery may consider the biological pH environment of the target in the disease process.
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spelling pubmed-93301792022-07-29 Discovery of pH-Selective Marine and Plant Natural Product Inhibitors of Cathepsin B Revealed by Screening at Acidic and Neutral pH Conditions Phan, Von V. Mosier, Charles Yoon, Michael C. Glukhov, Evgenia Caffrey, Conor R. O’Donoghue, Anthony J. Gerwick, William H. Hook, Vivian ACS Omega [Image: see text] Dysregulation of cathepsin B, which involves the translocation of the enzyme from acidic pH lysosomes to the neutral pH cytosol, followed by the initiation of cell death and inflammation, occurs in numerous brain disorders. The wide difference in the acidic pH (4.6) of lysosomes compared to the neutral pH (7.2) of the cytosol suggests that screening at different pH conditions may identify pH-selective modulators of cathepsin B. Therefore, a collection of pure marine and plant natural product (NP) compounds, with synthetic compounds, was screened at pH 4.6 and pH 7.2 in cathepsin B assays, which led to the identification of GER-12 (Crossbyanol B) and GER-24 ((7Z,9Z,12Z)-octadeca-7,9,12-trien-5-ynoic acid) marine NP inhibitors at acidic pH but not at neutral pH. GER-12 was effective for the reversible inhibition of cathepsin B, with an IC(50) of 3 μM. GER-24 had an IC(50) of 16 μM and was found to be an irreversible inhibitor. These results show that NP screening at distinct biological pH conditions can lead to the identification of pH-selective cathepsin B modulators. These findings suggest that screening efforts for molecular probes and drug discovery may consider the biological pH environment of the target in the disease process. American Chemical Society 2022-07-12 /pmc/articles/PMC9330179/ /pubmed/35910167 http://dx.doi.org/10.1021/acsomega.2c02287 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Phan, Von V.
Mosier, Charles
Yoon, Michael C.
Glukhov, Evgenia
Caffrey, Conor R.
O’Donoghue, Anthony J.
Gerwick, William H.
Hook, Vivian
Discovery of pH-Selective Marine and Plant Natural Product Inhibitors of Cathepsin B Revealed by Screening at Acidic and Neutral pH Conditions
title Discovery of pH-Selective Marine and Plant Natural Product Inhibitors of Cathepsin B Revealed by Screening at Acidic and Neutral pH Conditions
title_full Discovery of pH-Selective Marine and Plant Natural Product Inhibitors of Cathepsin B Revealed by Screening at Acidic and Neutral pH Conditions
title_fullStr Discovery of pH-Selective Marine and Plant Natural Product Inhibitors of Cathepsin B Revealed by Screening at Acidic and Neutral pH Conditions
title_full_unstemmed Discovery of pH-Selective Marine and Plant Natural Product Inhibitors of Cathepsin B Revealed by Screening at Acidic and Neutral pH Conditions
title_short Discovery of pH-Selective Marine and Plant Natural Product Inhibitors of Cathepsin B Revealed by Screening at Acidic and Neutral pH Conditions
title_sort discovery of ph-selective marine and plant natural product inhibitors of cathepsin b revealed by screening at acidic and neutral ph conditions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330179/
https://www.ncbi.nlm.nih.gov/pubmed/35910167
http://dx.doi.org/10.1021/acsomega.2c02287
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