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
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/14281
Ver los metadatos del registro completo
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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 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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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 |
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eng |
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eng |
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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 |
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openAccess |
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application/pdf application/pdf |
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Wiley |
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Wiley |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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