Functional multimerization of mucolipin channel proteins

Autores
Curcio Morelli, Cyntia; Zhang, Peng; Venugopal, Bhuvarahamurthy; Charles, Florie A.; Browning, Marsha F.; Cantiello, Horacio Fabio; Slaugenhaupt, Susan A.
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
MCOLN1 encodes mucolipin-1 (TRPML1), a member of the transient receptor potential TRPML subfamily of channel proteins. Mutations in MCOLN1 cause mucolipidosis-type IV (MLIV), a lysosomal storage disorder characterized by severe neurologic, ophthalmologic, and gastrointestinal abnormalities. Along with TRPML1, there are two other TRPML family members, mucolipin-2 (TRPML2) and mucolipin-3 (TRPML3). In this study, we used immunocytochemical analysis to determine that TRPML1, TRPML2, and TRPML3 co-localize in cells. The multimerization of TRPML proteins was confirmed by co-immunoprecipitation and Western blot analysis, which demonstrated that TRPML1 homo-multimerizes as well as hetero-multimerizes with TRPML2 and TRPML3. MLIV-causing mutants of TRPML1 also interacted with wild-type TRPML1. Lipid bilayer re-constitution of in vitro translated TRPML2 and TRPML3 confirmed their cation channel properties with lower single channel conductance and higher partial permeability to anions as compared to TRPML1. We further analyzed the electrophysiological properties of single channel TRPML hetero-multimers, which displayed functional differences when compared to individual TRPMLs. Our data shows for the first time that TRPMLs form distinct functional channel complexes. Homo- and hetero-multimerization of TRPMLs may modulate channel function and biophysical properties, thereby increasing TRPML functional diversity.
Fil: Curcio Morelli, Cyntia. Harvard Medical School; Estados Unidos
Fil: Zhang, Peng. Massachusetts General Hospital East; Estados Unidos
Fil: Venugopal, Bhuvarahamurthy. Harvard Medical School; Estados Unidos
Fil: Charles, Florie A.. Harvard Medical School; Estados Unidos
Fil: Browning, Marsha F.. Harvard Medical School; Estados Unidos
Fil: Cantiello, Horacio Fabio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Massachusetts General Hospital East; Estados Unidos
Fil: Slaugenhaupt, Susan A.. Harvard Medical School; Estados Unidos
Materia
Ml1
Multimerization
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/14281

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spelling Functional multimerization of mucolipin channel proteinsCurcio Morelli, CyntiaZhang, PengVenugopal, BhuvarahamurthyCharles, Florie A.Browning, Marsha F.Cantiello, Horacio FabioSlaugenhaupt, Susan A.Ml1Multimerizationhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3MCOLN1 encodes mucolipin-1 (TRPML1), a member of the transient receptor potential TRPML subfamily of channel proteins. Mutations in MCOLN1 cause mucolipidosis-type IV (MLIV), a lysosomal storage disorder characterized by severe neurologic, ophthalmologic, and gastrointestinal abnormalities. Along with TRPML1, there are two other TRPML family members, mucolipin-2 (TRPML2) and mucolipin-3 (TRPML3). In this study, we used immunocytochemical analysis to determine that TRPML1, TRPML2, and TRPML3 co-localize in cells. The multimerization of TRPML proteins was confirmed by co-immunoprecipitation and Western blot analysis, which demonstrated that TRPML1 homo-multimerizes as well as hetero-multimerizes with TRPML2 and TRPML3. MLIV-causing mutants of TRPML1 also interacted with wild-type TRPML1. Lipid bilayer re-constitution of in vitro translated TRPML2 and TRPML3 confirmed their cation channel properties with lower single channel conductance and higher partial permeability to anions as compared to TRPML1. We further analyzed the electrophysiological properties of single channel TRPML hetero-multimers, which displayed functional differences when compared to individual TRPMLs. Our data shows for the first time that TRPMLs form distinct functional channel complexes. Homo- and hetero-multimerization of TRPMLs may modulate channel function and biophysical properties, thereby increasing TRPML functional diversity.Fil: Curcio Morelli, Cyntia. Harvard Medical School; Estados UnidosFil: Zhang, Peng. Massachusetts General Hospital East; Estados UnidosFil: Venugopal, Bhuvarahamurthy. Harvard Medical School; Estados UnidosFil: Charles, Florie A.. Harvard Medical School; Estados UnidosFil: Browning, Marsha F.. Harvard Medical School; Estados UnidosFil: Cantiello, Horacio Fabio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Massachusetts General Hospital East; Estados UnidosFil: Slaugenhaupt, Susan A.. Harvard Medical School; Estados UnidosWiley2010-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/14281Curcio Morelli, Cyntia; Zhang, Peng; Venugopal, Bhuvarahamurthy; Charles, Florie A.; Browning, Marsha F.; et al.; Functional multimerization of mucolipin channel proteins; Wiley; Journal of Cellular Physiology; 222; 2; 2-2010; 328-3350021-95411097-4652enginfo:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/jcp.21956/abstractinfo:eu-repo/semantics/altIdentifier/doi/10.1002/jcp.21956info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T12:22:21Zoai:ri.conicet.gov.ar:11336/14281instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 12:22:21.78CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Functional multimerization of mucolipin channel proteins
title Functional multimerization of mucolipin channel proteins
spellingShingle Functional multimerization of mucolipin channel proteins
Curcio Morelli, Cyntia
Ml1
Multimerization
title_short Functional multimerization of mucolipin channel proteins
title_full Functional multimerization of mucolipin channel proteins
title_fullStr Functional multimerization of mucolipin channel proteins
title_full_unstemmed Functional multimerization of mucolipin channel proteins
title_sort Functional multimerization of mucolipin channel proteins
dc.creator.none.fl_str_mv Curcio Morelli, Cyntia
Zhang, Peng
Venugopal, Bhuvarahamurthy
Charles, Florie A.
Browning, Marsha F.
Cantiello, Horacio Fabio
Slaugenhaupt, Susan A.
author Curcio Morelli, Cyntia
author_facet Curcio Morelli, Cyntia
Zhang, Peng
Venugopal, Bhuvarahamurthy
Charles, Florie A.
Browning, Marsha F.
Cantiello, Horacio Fabio
Slaugenhaupt, Susan A.
author_role author
author2 Zhang, Peng
Venugopal, Bhuvarahamurthy
Charles, Florie A.
Browning, Marsha F.
Cantiello, Horacio Fabio
Slaugenhaupt, Susan A.
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv Ml1
Multimerization
topic Ml1
Multimerization
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv MCOLN1 encodes mucolipin-1 (TRPML1), a member of the transient receptor potential TRPML subfamily of channel proteins. Mutations in MCOLN1 cause mucolipidosis-type IV (MLIV), a lysosomal storage disorder characterized by severe neurologic, ophthalmologic, and gastrointestinal abnormalities. Along with TRPML1, there are two other TRPML family members, mucolipin-2 (TRPML2) and mucolipin-3 (TRPML3). In this study, we used immunocytochemical analysis to determine that TRPML1, TRPML2, and TRPML3 co-localize in cells. The multimerization of TRPML proteins was confirmed by co-immunoprecipitation and Western blot analysis, which demonstrated that TRPML1 homo-multimerizes as well as hetero-multimerizes with TRPML2 and TRPML3. MLIV-causing mutants of TRPML1 also interacted with wild-type TRPML1. Lipid bilayer re-constitution of in vitro translated TRPML2 and TRPML3 confirmed their cation channel properties with lower single channel conductance and higher partial permeability to anions as compared to TRPML1. We further analyzed the electrophysiological properties of single channel TRPML hetero-multimers, which displayed functional differences when compared to individual TRPMLs. Our data shows for the first time that TRPMLs form distinct functional channel complexes. Homo- and hetero-multimerization of TRPMLs may modulate channel function and biophysical properties, thereby increasing TRPML functional diversity.
Fil: Curcio Morelli, Cyntia. Harvard Medical School; Estados Unidos
Fil: Zhang, Peng. Massachusetts General Hospital East; Estados Unidos
Fil: Venugopal, Bhuvarahamurthy. Harvard Medical School; Estados Unidos
Fil: Charles, Florie A.. Harvard Medical School; Estados Unidos
Fil: Browning, Marsha F.. Harvard Medical School; Estados Unidos
Fil: Cantiello, Horacio Fabio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Massachusetts General Hospital East; Estados Unidos
Fil: Slaugenhaupt, Susan A.. Harvard Medical School; Estados Unidos
description MCOLN1 encodes mucolipin-1 (TRPML1), a member of the transient receptor potential TRPML subfamily of channel proteins. Mutations in MCOLN1 cause mucolipidosis-type IV (MLIV), a lysosomal storage disorder characterized by severe neurologic, ophthalmologic, and gastrointestinal abnormalities. Along with TRPML1, there are two other TRPML family members, mucolipin-2 (TRPML2) and mucolipin-3 (TRPML3). In this study, we used immunocytochemical analysis to determine that TRPML1, TRPML2, and TRPML3 co-localize in cells. The multimerization of TRPML proteins was confirmed by co-immunoprecipitation and Western blot analysis, which demonstrated that TRPML1 homo-multimerizes as well as hetero-multimerizes with TRPML2 and TRPML3. MLIV-causing mutants of TRPML1 also interacted with wild-type TRPML1. Lipid bilayer re-constitution of in vitro translated TRPML2 and TRPML3 confirmed their cation channel properties with lower single channel conductance and higher partial permeability to anions as compared to TRPML1. We further analyzed the electrophysiological properties of single channel TRPML hetero-multimers, which displayed functional differences when compared to individual TRPMLs. Our data shows for the first time that TRPMLs form distinct functional channel complexes. Homo- and hetero-multimerization of TRPMLs may modulate channel function and biophysical properties, thereby increasing TRPML functional diversity.
publishDate 2010
dc.date.none.fl_str_mv 2010-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/14281
Curcio Morelli, Cyntia; Zhang, Peng; Venugopal, Bhuvarahamurthy; Charles, Florie A.; Browning, Marsha F.; et al.; Functional multimerization of mucolipin channel proteins; Wiley; Journal of Cellular Physiology; 222; 2; 2-2010; 328-335
0021-9541
1097-4652
url http://hdl.handle.net/11336/14281
identifier_str_mv Curcio Morelli, Cyntia; Zhang, Peng; Venugopal, Bhuvarahamurthy; Charles, Florie A.; Browning, Marsha F.; et al.; Functional multimerization of mucolipin channel proteins; Wiley; Journal of Cellular Physiology; 222; 2; 2-2010; 328-335
0021-9541
1097-4652
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/jcp.21956/abstract
info:eu-repo/semantics/altIdentifier/doi/10.1002/jcp.21956
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
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instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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