Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784758099610959872 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9330179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT phanvonv discoveryofphselectivemarineandplantnaturalproductinhibitorsofcathepsinbrevealedbyscreeningatacidicandneutralphconditions AT mosiercharles discoveryofphselectivemarineandplantnaturalproductinhibitorsofcathepsinbrevealedbyscreeningatacidicandneutralphconditions AT yoonmichaelc discoveryofphselectivemarineandplantnaturalproductinhibitorsofcathepsinbrevealedbyscreeningatacidicandneutralphconditions AT glukhovevgenia discoveryofphselectivemarineandplantnaturalproductinhibitorsofcathepsinbrevealedbyscreeningatacidicandneutralphconditions AT caffreyconorr discoveryofphselectivemarineandplantnaturalproductinhibitorsofcathepsinbrevealedbyscreeningatacidicandneutralphconditions AT odonoghueanthonyj discoveryofphselectivemarineandplantnaturalproductinhibitorsofcathepsinbrevealedbyscreeningatacidicandneutralphconditions AT gerwickwilliamh discoveryofphselectivemarineandplantnaturalproductinhibitorsofcathepsinbrevealedbyscreeningatacidicandneutralphconditions AT hookvivian discoveryofphselectivemarineandplantnaturalproductinhibitorsofcathepsinbrevealedbyscreeningatacidicandneutralphconditions |