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Functionally coupled ion channels begin co-assembling at the start of their synthesis
by
Moreno, Claudia M
, Huang, Jessica M
, Vivas, Oscar
, Ma, Michael
, Pournejati, Roya
in
Animals
/ BK channel
/ Calcium Channels
/ Calcium channels (voltage-gated)
/ Calcium Channels, L-Type - biosynthesis
/ Calcium Channels, L-Type - genetics
/ Calcium Channels, L-Type - metabolism
/ Calcium permeability
/ Cell Biology
/ Cell Membrane - metabolism
/ clustering
/ Endoplasmic reticulum
/ Endoplasmic Reticulum - metabolism
/ functional coupling
/ Golgi apparatus
/ Golgi Apparatus - metabolism
/ Humans
/ Hypotheses
/ Ion channels
/ Large-Conductance Calcium-Activated Potassium Channels - biosynthesis
/ Large-Conductance Calcium-Activated Potassium Channels - genetics
/ Large-Conductance Calcium-Activated Potassium Channels - metabolism
/ Membranes
/ Physiology
/ Plasma
/ Potassium
/ Potassium channels (calcium-gated)
/ Protein Binding
/ Protein Biosynthesis
/ Protein interaction
/ Protein Multimerization
/ Proteins
/ rat insulinoma cell line
/ Rats
/ RNA, Messenger - metabolism
/ Structural Biology and Molecular Biophysics
/ structural coupling
/ voltage-gated Ca channel
2026
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Functionally coupled ion channels begin co-assembling at the start of their synthesis
by
Moreno, Claudia M
, Huang, Jessica M
, Vivas, Oscar
, Ma, Michael
, Pournejati, Roya
in
Animals
/ BK channel
/ Calcium Channels
/ Calcium channels (voltage-gated)
/ Calcium Channels, L-Type - biosynthesis
/ Calcium Channels, L-Type - genetics
/ Calcium Channels, L-Type - metabolism
/ Calcium permeability
/ Cell Biology
/ Cell Membrane - metabolism
/ clustering
/ Endoplasmic reticulum
/ Endoplasmic Reticulum - metabolism
/ functional coupling
/ Golgi apparatus
/ Golgi Apparatus - metabolism
/ Humans
/ Hypotheses
/ Ion channels
/ Large-Conductance Calcium-Activated Potassium Channels - biosynthesis
/ Large-Conductance Calcium-Activated Potassium Channels - genetics
/ Large-Conductance Calcium-Activated Potassium Channels - metabolism
/ Membranes
/ Physiology
/ Plasma
/ Potassium
/ Potassium channels (calcium-gated)
/ Protein Binding
/ Protein Biosynthesis
/ Protein interaction
/ Protein Multimerization
/ Proteins
/ rat insulinoma cell line
/ Rats
/ RNA, Messenger - metabolism
/ Structural Biology and Molecular Biophysics
/ structural coupling
/ voltage-gated Ca channel
2026
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Functionally coupled ion channels begin co-assembling at the start of their synthesis
by
Moreno, Claudia M
, Huang, Jessica M
, Vivas, Oscar
, Ma, Michael
, Pournejati, Roya
in
Animals
/ BK channel
/ Calcium Channels
/ Calcium channels (voltage-gated)
/ Calcium Channels, L-Type - biosynthesis
/ Calcium Channels, L-Type - genetics
/ Calcium Channels, L-Type - metabolism
/ Calcium permeability
/ Cell Biology
/ Cell Membrane - metabolism
/ clustering
/ Endoplasmic reticulum
/ Endoplasmic Reticulum - metabolism
/ functional coupling
/ Golgi apparatus
/ Golgi Apparatus - metabolism
/ Humans
/ Hypotheses
/ Ion channels
/ Large-Conductance Calcium-Activated Potassium Channels - biosynthesis
/ Large-Conductance Calcium-Activated Potassium Channels - genetics
/ Large-Conductance Calcium-Activated Potassium Channels - metabolism
/ Membranes
/ Physiology
/ Plasma
/ Potassium
/ Potassium channels (calcium-gated)
/ Protein Binding
/ Protein Biosynthesis
/ Protein interaction
/ Protein Multimerization
/ Proteins
/ rat insulinoma cell line
/ Rats
/ RNA, Messenger - metabolism
/ Structural Biology and Molecular Biophysics
/ structural coupling
/ voltage-gated Ca channel
2026
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Functionally coupled ion channels begin co-assembling at the start of their synthesis
Journal Article
Functionally coupled ion channels begin co-assembling at the start of their synthesis
2026
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Overview
Calcium binding to BK channels lowers BK activation threshold, substantiating functional coupling with calcium-permeable channels. This coupling requires close proximity between different channel types, and the formation of BK-Ca V 1.3 hetero-clusters at nanometer distances exemplifies this unique organization. To investigate the structural basis of this interaction, we tested the hypothesis that BK and Ca V 1.3 channels assemble before their insertion into the plasma membrane. Our approach incorporated four strategies: (1) detecting interactions between BK and Ca V 1.3 proteins inside the cell, (2) identifying membrane compartments where intracellular hetero-clusters reside, (3) measuring the proximity of their mRNAs, and (4) assessing protein interactions at the plasma membrane during early translation. These analyses revealed that a subset of BK and Ca V 1.3 transcripts are spatially close in micro-translational complexes, and their newly synthesized proteins associate within the endoplasmic reticulum (ER) and Golgi. Comparisons with other proteins, transcripts, and randomized localization models support the conclusion that BK and Ca V 1.3 hetero-clusters form before their insertion at the plasma membrane.
Publisher
eLife Sciences Publications Ltd,eLife Sciences Publications, Ltd
Subject
/ Calcium channels (voltage-gated)
/ Calcium Channels, L-Type - biosynthesis
/ Calcium Channels, L-Type - genetics
/ Calcium Channels, L-Type - metabolism
/ Endoplasmic Reticulum - metabolism
/ Golgi Apparatus - metabolism
/ Humans
/ Large-Conductance Calcium-Activated Potassium Channels - biosynthesis
/ Large-Conductance Calcium-Activated Potassium Channels - genetics
/ Large-Conductance Calcium-Activated Potassium Channels - metabolism
/ Plasma
/ Potassium channels (calcium-gated)
/ Proteins
/ Rats
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