A Voltage-Gated H + Channel Underlying pH Homeostasis

Marine coccolithophorid phytoplankton are major producers of biogenic calcite, playing a significant role in the global carbon cycle. Predicting the impacts of ocean acidification on coccolithophore calcification has received much recent attention and requires improved knowledge of cellular calcific...

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Main Authors: In Calcifying Coccolithophores, Alison R. Taylor, Abdul Chrachri, Glen Wheeler, Helen Goddard, Colin Brownlee
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Online Access:http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.291.3138
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spelling ftciteseerx:oai:CiteSeerX.psu:10.1.1.291.3138 2023-05-15T17:51:22+02:00 A Voltage-Gated H + Channel Underlying pH Homeostasis In Calcifying Coccolithophores Alison R. Taylor Abdul Chrachri Glen Wheeler Helen Goddard Colin Brownlee The Pennsylvania State University CiteSeerX Archives application/zip http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.291.3138 en eng http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.291.3138 Metadata may be used without restrictions as long as the oai identifier remains attached to it. ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/5a/5e/PLoS_Biol_2011_Jun_21_9(6)_e1001085.tar.gz text ftciteseerx 2016-01-07T21:34:53Z Marine coccolithophorid phytoplankton are major producers of biogenic calcite, playing a significant role in the global carbon cycle. Predicting the impacts of ocean acidification on coccolithophore calcification has received much recent attention and requires improved knowledge of cellular calcification mechanisms. Uniquely amongst calcifying organisms, coccolithophores produce calcified scales (coccoliths) in an intracellular compartment and secrete them to the cell surface, requiring large transcellular ionic fluxes to support calcification. In particular, intracellular calcite precipitation using HCO 3 2 as the substrate generates equimolar quantities of H + that must be rapidly removed to prevent cytoplasmic acidification. We have used electrophysiological approaches to identify a plasma membrane voltage-gated H + conductance in Coccolithus pelagicus ssp braarudii with remarkably similar biophysical and functional properties to those found in metazoans. We show that both C. pelagicus and Emiliania huxleyi possess homologues of metazoan H v1H + channels, which function as voltagegated H + channels when expressed in heterologous systems. Homologues of the coccolithophore H + channels were also identified in a diversity of eukaryotes, suggesting a wide range of cellular roles for the Hv1 class of proteins. Using single cell imaging, we demonstrate that the coccolithophore H + conductance mediates rapid H + efflux and plays an important role in pH homeostasis in calcifying cells. The results demonstrate a novel cellular role for voltage gated H + channels and provide Text Ocean acidification Unknown
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description Marine coccolithophorid phytoplankton are major producers of biogenic calcite, playing a significant role in the global carbon cycle. Predicting the impacts of ocean acidification on coccolithophore calcification has received much recent attention and requires improved knowledge of cellular calcification mechanisms. Uniquely amongst calcifying organisms, coccolithophores produce calcified scales (coccoliths) in an intracellular compartment and secrete them to the cell surface, requiring large transcellular ionic fluxes to support calcification. In particular, intracellular calcite precipitation using HCO 3 2 as the substrate generates equimolar quantities of H + that must be rapidly removed to prevent cytoplasmic acidification. We have used electrophysiological approaches to identify a plasma membrane voltage-gated H + conductance in Coccolithus pelagicus ssp braarudii with remarkably similar biophysical and functional properties to those found in metazoans. We show that both C. pelagicus and Emiliania huxleyi possess homologues of metazoan H v1H + channels, which function as voltagegated H + channels when expressed in heterologous systems. Homologues of the coccolithophore H + channels were also identified in a diversity of eukaryotes, suggesting a wide range of cellular roles for the Hv1 class of proteins. Using single cell imaging, we demonstrate that the coccolithophore H + conductance mediates rapid H + efflux and plays an important role in pH homeostasis in calcifying cells. The results demonstrate a novel cellular role for voltage gated H + channels and provide
author2 The Pennsylvania State University CiteSeerX Archives
format Text
author In Calcifying Coccolithophores
Alison R. Taylor
Abdul Chrachri
Glen Wheeler
Helen Goddard
Colin Brownlee
spellingShingle In Calcifying Coccolithophores
Alison R. Taylor
Abdul Chrachri
Glen Wheeler
Helen Goddard
Colin Brownlee
A Voltage-Gated H + Channel Underlying pH Homeostasis
author_facet In Calcifying Coccolithophores
Alison R. Taylor
Abdul Chrachri
Glen Wheeler
Helen Goddard
Colin Brownlee
author_sort In Calcifying Coccolithophores
title A Voltage-Gated H + Channel Underlying pH Homeostasis
title_short A Voltage-Gated H + Channel Underlying pH Homeostasis
title_full A Voltage-Gated H + Channel Underlying pH Homeostasis
title_fullStr A Voltage-Gated H + Channel Underlying pH Homeostasis
title_full_unstemmed A Voltage-Gated H + Channel Underlying pH Homeostasis
title_sort voltage-gated h + channel underlying ph homeostasis
url http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.291.3138
genre Ocean acidification
genre_facet Ocean acidification
op_source ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/5a/5e/PLoS_Biol_2011_Jun_21_9(6)_e1001085.tar.gz
op_relation http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.291.3138
op_rights Metadata may be used without restrictions as long as the oai identifier remains attached to it.
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