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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/244819

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network_name_str CONICET Digital (CONICET)
spelling 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)
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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