Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor
- Autores
- Mukhtasimova, Nuriya; Bouzat, Cecilia Beatriz; Sine, Steve M.
- Año de publicación
- 2024
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Drug modulation of the α7 acetylcholine receptor has emerged as a therapeutic strategy for neurological, neurodegenerative, and infammatory disorders. α7 is a homo-pentamer containing topographically distinct sites for agonists, calcium, and drug modulators with each type of site present in fve copies. However, functional relationships between agonist, calcium, and drug modulator sites remain poorly understood. To investigate these relationships, we manipulated the number of agonist binding sites, and monitored potentiation of ACh-elicited single-channel currents through α7 receptors by PNU-120596 (PNU) both in the presence and absence of calcium. When ACh is present alone, it elicits brief, sub-millisecond channel openings, however when ACh is present with PNU it elicits long clusters of potentiated openings. In receptors harboring fve agonist binding sites, PNU potentiates regardless of the presence or absence of calcium, whereas in receptors harboring one agonist binding site, PNU potentiates in the presence but not the absence of calcium. By varying the numbers of agonist and calcium binding sites we show that PNU potentiation of α7 depends on a balance between agonist occupancy of the orthosteric sites and calcium occupancy of the allosteric sites. The fndings suggest that in the local cellular environment, fuctuations in the concentrations of neurotransmitter and calcium may alter this balance and modulate the ability of PNU to potentiate α7
Fil: Mukhtasimova, Nuriya. Mayo Clinic College of Medicine and Science; Estados Unidos
Fil: Bouzat, Cecilia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Sine, Steve M.. Mayo Clinic College of Medicine and Science; Estados Unidos - Materia
-
NICOTINIC RECEPTOR
POSITIVE ALLOSTERIC MODULATOR
SINGLE ION CHANNEL RECORDING
PATCH CLAMP
LIGAND-GATED ION CHANNEL - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/244819
Ver los metadatos del registro completo
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Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptorMukhtasimova, NuriyaBouzat, Cecilia BeatrizSine, Steve M.NICOTINIC RECEPTORPOSITIVE ALLOSTERIC MODULATORSINGLE ION CHANNEL RECORDINGPATCH CLAMPLIGAND-GATED ION CHANNELhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Drug modulation of the α7 acetylcholine receptor has emerged as a therapeutic strategy for neurological, neurodegenerative, and infammatory disorders. α7 is a homo-pentamer containing topographically distinct sites for agonists, calcium, and drug modulators with each type of site present in fve copies. However, functional relationships between agonist, calcium, and drug modulator sites remain poorly understood. To investigate these relationships, we manipulated the number of agonist binding sites, and monitored potentiation of ACh-elicited single-channel currents through α7 receptors by PNU-120596 (PNU) both in the presence and absence of calcium. When ACh is present alone, it elicits brief, sub-millisecond channel openings, however when ACh is present with PNU it elicits long clusters of potentiated openings. In receptors harboring fve agonist binding sites, PNU potentiates regardless of the presence or absence of calcium, whereas in receptors harboring one agonist binding site, PNU potentiates in the presence but not the absence of calcium. By varying the numbers of agonist and calcium binding sites we show that PNU potentiation of α7 depends on a balance between agonist occupancy of the orthosteric sites and calcium occupancy of the allosteric sites. The fndings suggest that in the local cellular environment, fuctuations in the concentrations of neurotransmitter and calcium may alter this balance and modulate the ability of PNU to potentiate α7Fil: Mukhtasimova, Nuriya. Mayo Clinic College of Medicine and Science; Estados UnidosFil: Bouzat, Cecilia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Sine, Steve M.. Mayo Clinic College of Medicine and Science; Estados UnidosSpringer Nature2024-08-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/244819Mukhtasimova, Nuriya; Bouzat, Cecilia Beatriz; Sine, Steve M.; Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor; Springer Nature; Cellular And Molecular Life Sciences; 81; 332; 7-8-2024; 1-171420-682X1420-9071CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007/s00018-024-05374-1info:eu-repo/semantics/altIdentifier/doi/10.1007/s00018-024-05374-1info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:12:24Zoai:ri.conicet.gov.ar:11336/244819instacron: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:34982025-09-10 13:12:25.017CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor |
title |
Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor |
spellingShingle |
Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor Mukhtasimova, Nuriya NICOTINIC RECEPTOR POSITIVE ALLOSTERIC MODULATOR SINGLE ION CHANNEL RECORDING PATCH CLAMP LIGAND-GATED ION CHANNEL |
title_short |
Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor |
title_full |
Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor |
title_fullStr |
Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor |
title_full_unstemmed |
Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor |
title_sort |
Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor |
dc.creator.none.fl_str_mv |
Mukhtasimova, Nuriya Bouzat, Cecilia Beatriz Sine, Steve M. |
author |
Mukhtasimova, Nuriya |
author_facet |
Mukhtasimova, Nuriya Bouzat, Cecilia Beatriz Sine, Steve M. |
author_role |
author |
author2 |
Bouzat, Cecilia Beatriz Sine, Steve M. |
author2_role |
author author |
dc.subject.none.fl_str_mv |
NICOTINIC RECEPTOR POSITIVE ALLOSTERIC MODULATOR SINGLE ION CHANNEL RECORDING PATCH CLAMP LIGAND-GATED ION CHANNEL |
topic |
NICOTINIC RECEPTOR POSITIVE ALLOSTERIC MODULATOR SINGLE ION CHANNEL RECORDING PATCH CLAMP LIGAND-GATED ION CHANNEL |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Drug modulation of the α7 acetylcholine receptor has emerged as a therapeutic strategy for neurological, neurodegenerative, and infammatory disorders. α7 is a homo-pentamer containing topographically distinct sites for agonists, calcium, and drug modulators with each type of site present in fve copies. However, functional relationships between agonist, calcium, and drug modulator sites remain poorly understood. To investigate these relationships, we manipulated the number of agonist binding sites, and monitored potentiation of ACh-elicited single-channel currents through α7 receptors by PNU-120596 (PNU) both in the presence and absence of calcium. When ACh is present alone, it elicits brief, sub-millisecond channel openings, however when ACh is present with PNU it elicits long clusters of potentiated openings. In receptors harboring fve agonist binding sites, PNU potentiates regardless of the presence or absence of calcium, whereas in receptors harboring one agonist binding site, PNU potentiates in the presence but not the absence of calcium. By varying the numbers of agonist and calcium binding sites we show that PNU potentiation of α7 depends on a balance between agonist occupancy of the orthosteric sites and calcium occupancy of the allosteric sites. The fndings suggest that in the local cellular environment, fuctuations in the concentrations of neurotransmitter and calcium may alter this balance and modulate the ability of PNU to potentiate α7 Fil: Mukhtasimova, Nuriya. Mayo Clinic College of Medicine and Science; Estados Unidos Fil: Bouzat, Cecilia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina Fil: Sine, Steve M.. Mayo Clinic College of Medicine and Science; Estados Unidos |
description |
Drug modulation of the α7 acetylcholine receptor has emerged as a therapeutic strategy for neurological, neurodegenerative, and infammatory disorders. α7 is a homo-pentamer containing topographically distinct sites for agonists, calcium, and drug modulators with each type of site present in fve copies. However, functional relationships between agonist, calcium, and drug modulator sites remain poorly understood. To investigate these relationships, we manipulated the number of agonist binding sites, and monitored potentiation of ACh-elicited single-channel currents through α7 receptors by PNU-120596 (PNU) both in the presence and absence of calcium. When ACh is present alone, it elicits brief, sub-millisecond channel openings, however when ACh is present with PNU it elicits long clusters of potentiated openings. In receptors harboring fve agonist binding sites, PNU potentiates regardless of the presence or absence of calcium, whereas in receptors harboring one agonist binding site, PNU potentiates in the presence but not the absence of calcium. By varying the numbers of agonist and calcium binding sites we show that PNU potentiation of α7 depends on a balance between agonist occupancy of the orthosteric sites and calcium occupancy of the allosteric sites. The fndings suggest that in the local cellular environment, fuctuations in the concentrations of neurotransmitter and calcium may alter this balance and modulate the ability of PNU to potentiate α7 |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-08-07 |
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/11336/244819 Mukhtasimova, Nuriya; Bouzat, Cecilia Beatriz; Sine, Steve M.; Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor; Springer Nature; Cellular And Molecular Life Sciences; 81; 332; 7-8-2024; 1-17 1420-682X 1420-9071 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/244819 |
identifier_str_mv |
Mukhtasimova, Nuriya; Bouzat, Cecilia Beatriz; Sine, Steve M.; Novel interplay between agonist and calcium binding sites modulates drug potentiation of α7 acetylcholine receptor; Springer Nature; Cellular And Molecular Life Sciences; 81; 332; 7-8-2024; 1-17 1420-682X 1420-9071 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007/s00018-024-05374-1 info:eu-repo/semantics/altIdentifier/doi/10.1007/s00018-024-05374-1 |
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 |
Springer Nature |
publisher.none.fl_str_mv |
Springer Nature |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
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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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1842980646405799936 |
score |
13.004268 |