Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates

Bibliographic Details
Main Author: Aureliano, Manuel
Publication Date: 2022
Other Authors: Fraqueza, Gil, Berrocal, Maria, Cordoba-Granados, Juan J., Gumerova, Nadiia I., Rompel, Annette, Gutierrez-Merino, Carlos, Mata, Ana M.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.1/18943
Summary: Plasma membrane calcium ATPases (PMCA) and sarco(endo) reticulum calcium ATPases (SERCA) are key proteins in the maintenance of calcium homeostasis. Herein, we compare for the first time the inhibition of SERCA and PMCA calcium pumps by several polyoxotungstates (POTs), namely by Wells-Dawson phospho-tungstate anions [P2W18O62]6-(intact, {P2W18}), [P2W17O61]10-(monolacunary, {P2W17}), [P2W15O56]12-(trilacunary, {P2W15}), [H2P2W12O48]12-(hexalacunary, {P2W12}), [H3P2W15V3O62]6- (trivanadium-substituted, {P2W15V3}) and by Preyssler-type anion [NaP5W30O110]14-({P5W30}). The speciation in the solu-tions of tested POTs was investigated by 31P and 51V NMR spectroscopy. The tested POTs inhibited SERCA Ca2+- ATPase activity, whereby the Preyssler POT showed the strongest effect, with an IC50 value of 0.37 mu M. For {P2W17} and {P2W15V3} higher IC50 values were determined: 0.72 and 0.95 mu M, respectively. The studied POTs showed to be more potent inhibitors of PMCA Ca2+-ATPase activity, with lower IC50 values for {P2W17}, {P5W30} and {P2W15V3}.
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spelling Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstatesPolyoxometalatesPolyoxometalate?s stabilityCa2+-ATPaseATPases inhibitorsAnticancer drugsDrug discoveryPlasma membrane calcium ATPases (PMCA) and sarco(endo) reticulum calcium ATPases (SERCA) are key proteins in the maintenance of calcium homeostasis. Herein, we compare for the first time the inhibition of SERCA and PMCA calcium pumps by several polyoxotungstates (POTs), namely by Wells-Dawson phospho-tungstate anions [P2W18O62]6-(intact, {P2W18}), [P2W17O61]10-(monolacunary, {P2W17}), [P2W15O56]12-(trilacunary, {P2W15}), [H2P2W12O48]12-(hexalacunary, {P2W12}), [H3P2W15V3O62]6- (trivanadium-substituted, {P2W15V3}) and by Preyssler-type anion [NaP5W30O110]14-({P5W30}). The speciation in the solu-tions of tested POTs was investigated by 31P and 51V NMR spectroscopy. The tested POTs inhibited SERCA Ca2+- ATPase activity, whereby the Preyssler POT showed the strongest effect, with an IC50 value of 0.37 mu M. For {P2W17} and {P2W15V3} higher IC50 values were determined: 0.72 and 0.95 mu M, respectively. The studied POTs showed to be more potent inhibitors of PMCA Ca2+-ATPase activity, with lower IC50 values for {P2W17}, {P5W30} and {P2W15V3}.ElsevierSapientiaAureliano, ManuelFraqueza, GilBerrocal, MariaCordoba-Granados, Juan J.Gumerova, Nadiia I.Rompel, AnnetteGutierrez-Merino, CarlosMata, Ana M.2023-01-26T14:19:33Z2022-082022-08-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/18943eng10.1016/j.jinorgbio.2022.111952info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-18T17:12:17Zoai:sapientia.ualg.pt:10400.1/18943Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T20:13:46.256730Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates
title Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates
spellingShingle Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates
Aureliano, Manuel
Polyoxometalates
Polyoxometalate?s stability
Ca2+-ATPase
ATPases inhibitors
Anticancer drugs
Drug discovery
title_short Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates
title_full Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates
title_fullStr Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates
title_full_unstemmed Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates
title_sort Inhibition of SERCA and PMCA Ca2+-ATPase activities by polyoxotungstates
author Aureliano, Manuel
author_facet Aureliano, Manuel
Fraqueza, Gil
Berrocal, Maria
Cordoba-Granados, Juan J.
Gumerova, Nadiia I.
Rompel, Annette
Gutierrez-Merino, Carlos
Mata, Ana M.
author_role author
author2 Fraqueza, Gil
Berrocal, Maria
Cordoba-Granados, Juan J.
Gumerova, Nadiia I.
Rompel, Annette
Gutierrez-Merino, Carlos
Mata, Ana M.
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Sapientia
dc.contributor.author.fl_str_mv Aureliano, Manuel
Fraqueza, Gil
Berrocal, Maria
Cordoba-Granados, Juan J.
Gumerova, Nadiia I.
Rompel, Annette
Gutierrez-Merino, Carlos
Mata, Ana M.
dc.subject.por.fl_str_mv Polyoxometalates
Polyoxometalate?s stability
Ca2+-ATPase
ATPases inhibitors
Anticancer drugs
Drug discovery
topic Polyoxometalates
Polyoxometalate?s stability
Ca2+-ATPase
ATPases inhibitors
Anticancer drugs
Drug discovery
description Plasma membrane calcium ATPases (PMCA) and sarco(endo) reticulum calcium ATPases (SERCA) are key proteins in the maintenance of calcium homeostasis. Herein, we compare for the first time the inhibition of SERCA and PMCA calcium pumps by several polyoxotungstates (POTs), namely by Wells-Dawson phospho-tungstate anions [P2W18O62]6-(intact, {P2W18}), [P2W17O61]10-(monolacunary, {P2W17}), [P2W15O56]12-(trilacunary, {P2W15}), [H2P2W12O48]12-(hexalacunary, {P2W12}), [H3P2W15V3O62]6- (trivanadium-substituted, {P2W15V3}) and by Preyssler-type anion [NaP5W30O110]14-({P5W30}). The speciation in the solu-tions of tested POTs was investigated by 31P and 51V NMR spectroscopy. The tested POTs inhibited SERCA Ca2+- ATPase activity, whereby the Preyssler POT showed the strongest effect, with an IC50 value of 0.37 mu M. For {P2W17} and {P2W15V3} higher IC50 values were determined: 0.72 and 0.95 mu M, respectively. The studied POTs showed to be more potent inhibitors of PMCA Ca2+-ATPase activity, with lower IC50 values for {P2W17}, {P5W30} and {P2W15V3}.
publishDate 2022
dc.date.none.fl_str_mv 2022-08
2022-08-01T00:00:00Z
2023-01-26T14:19:33Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.1/18943
url http://hdl.handle.net/10400.1/18943
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.jinorgbio.2022.111952
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
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