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Demonstration of Binding of Neuronal Calcium Sensor-1 to the Ca(v)2.1 P/Q-Type Calcium Channel
[Image: see text] In neurons, entry of extracellular calcium (Ca(2+)) into synaptic terminals through Ca(v)2.1 (P/Q-type) Ca(2+) channels is the driving force for exocytosis of neurotransmitter-containing synaptic vesicles. This class of Ca(2+) channel is, therefore, pivotal during normal neurotrans...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180279/ https://www.ncbi.nlm.nih.gov/pubmed/25188201 http://dx.doi.org/10.1021/bi500568v |
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author | Lian, Lu-Yun Pandalaneni, Sravan R. Todd, Paul A. C. Martin, Victoria M. Burgoyne, Robert D. Haynes, Lee P. |
author_facet | Lian, Lu-Yun Pandalaneni, Sravan R. Todd, Paul A. C. Martin, Victoria M. Burgoyne, Robert D. Haynes, Lee P. |
author_sort | Lian, Lu-Yun |
collection | PubMed |
description | [Image: see text] In neurons, entry of extracellular calcium (Ca(2+)) into synaptic terminals through Ca(v)2.1 (P/Q-type) Ca(2+) channels is the driving force for exocytosis of neurotransmitter-containing synaptic vesicles. This class of Ca(2+) channel is, therefore, pivotal during normal neurotransmission in higher organisms. In response to channel opening and Ca(2+) influx, specific Ca(2+)-binding proteins associate with cytoplasmic regulatory domains of the P/Q channel to modulate subsequent channel opening. Channel modulation in this way influences synaptic plasticity with consequences for higher-level processes such as learning and memory acquisition. The ubiquitous Ca(2+)-sensing protein calmodulin (CaM) regulates the activity of all types of mammalian voltage-gated Ca(2+) channels, including the P/Q class, by direct binding to specific regulatory motifs. More recently, experimental evidence has highlighted a role for additional Ca(2+)-binding proteins, particularly of the CaBP and NCS families in the regulation of P/Q channels. NCS-1 is a protein found from yeast to humans and that regulates a diverse number of cellular functions. Physiological and genetic evidence indicates that NCS-1 regulates P/Q channel activity, including calcium-dependent facilitation, although a direct physical association between the proteins has yet to be demonstrated. In this study, we aimed to determine if there is a direct interaction between NCS-1 and the C-terminal cytoplasmic tail of the Ca(v)2.1 α-subunit. Using distinct but complementary approaches, including in vitro binding of bacterially expressed recombinant proteins, fluorescence spectrophotometry, isothermal titration calorimetry, nuclear magnetic resonance, and expression of fluorescently tagged proteins in mammalian cells, we show direct binding and demonstrate that CaM can compete for it. We speculate about how NCS-1/Ca(v)2.1 association might add to the complexity of calcium channel regulation mediated by other known calcium-sensing proteins and how this might help to fine-tune neurotransmission in the mammalian central nervous system. |
format | Online Article Text |
id | pubmed-4180279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41802792014-10-02 Demonstration of Binding of Neuronal Calcium Sensor-1 to the Ca(v)2.1 P/Q-Type Calcium Channel Lian, Lu-Yun Pandalaneni, Sravan R. Todd, Paul A. C. Martin, Victoria M. Burgoyne, Robert D. Haynes, Lee P. Biochemistry [Image: see text] In neurons, entry of extracellular calcium (Ca(2+)) into synaptic terminals through Ca(v)2.1 (P/Q-type) Ca(2+) channels is the driving force for exocytosis of neurotransmitter-containing synaptic vesicles. This class of Ca(2+) channel is, therefore, pivotal during normal neurotransmission in higher organisms. In response to channel opening and Ca(2+) influx, specific Ca(2+)-binding proteins associate with cytoplasmic regulatory domains of the P/Q channel to modulate subsequent channel opening. Channel modulation in this way influences synaptic plasticity with consequences for higher-level processes such as learning and memory acquisition. The ubiquitous Ca(2+)-sensing protein calmodulin (CaM) regulates the activity of all types of mammalian voltage-gated Ca(2+) channels, including the P/Q class, by direct binding to specific regulatory motifs. More recently, experimental evidence has highlighted a role for additional Ca(2+)-binding proteins, particularly of the CaBP and NCS families in the regulation of P/Q channels. NCS-1 is a protein found from yeast to humans and that regulates a diverse number of cellular functions. Physiological and genetic evidence indicates that NCS-1 regulates P/Q channel activity, including calcium-dependent facilitation, although a direct physical association between the proteins has yet to be demonstrated. In this study, we aimed to determine if there is a direct interaction between NCS-1 and the C-terminal cytoplasmic tail of the Ca(v)2.1 α-subunit. Using distinct but complementary approaches, including in vitro binding of bacterially expressed recombinant proteins, fluorescence spectrophotometry, isothermal titration calorimetry, nuclear magnetic resonance, and expression of fluorescently tagged proteins in mammalian cells, we show direct binding and demonstrate that CaM can compete for it. We speculate about how NCS-1/Ca(v)2.1 association might add to the complexity of calcium channel regulation mediated by other known calcium-sensing proteins and how this might help to fine-tune neurotransmission in the mammalian central nervous system. American Chemical Society 2014-09-04 2014-09-30 /pmc/articles/PMC4180279/ /pubmed/25188201 http://dx.doi.org/10.1021/bi500568v Text en Copyright © 2014 American Chemical Society Terms of Use CC-BY (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) |
spellingShingle | Lian, Lu-Yun Pandalaneni, Sravan R. Todd, Paul A. C. Martin, Victoria M. Burgoyne, Robert D. Haynes, Lee P. Demonstration of Binding of Neuronal Calcium Sensor-1 to the Ca(v)2.1 P/Q-Type Calcium Channel |
title | Demonstration of Binding of Neuronal Calcium Sensor-1
to the Ca(v)2.1 P/Q-Type Calcium Channel |
title_full | Demonstration of Binding of Neuronal Calcium Sensor-1
to the Ca(v)2.1 P/Q-Type Calcium Channel |
title_fullStr | Demonstration of Binding of Neuronal Calcium Sensor-1
to the Ca(v)2.1 P/Q-Type Calcium Channel |
title_full_unstemmed | Demonstration of Binding of Neuronal Calcium Sensor-1
to the Ca(v)2.1 P/Q-Type Calcium Channel |
title_short | Demonstration of Binding of Neuronal Calcium Sensor-1
to the Ca(v)2.1 P/Q-Type Calcium Channel |
title_sort | demonstration of binding of neuronal calcium sensor-1
to the ca(v)2.1 p/q-type calcium channel |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180279/ https://www.ncbi.nlm.nih.gov/pubmed/25188201 http://dx.doi.org/10.1021/bi500568v |
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