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Membrane Dynamics and Calcium Signaling

Overview of attention for book
Cover of 'Membrane Dynamics and Calcium Signaling'

Table of Contents

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    Book Overview
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    Chapter 1 The Plasma Membrane Calcium Pump (PMCA): Regulation of Cytosolic Ca 2+ , Genetic Diversities and Its Role in Sub-plasma Membrane Microdomains
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    Chapter 2 Structure-Function Relationship of the Voltage-Gated Calcium Channel Ca v 1.1 Complex
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    Chapter 3 Structure-Dynamic Coupling Through Ca 2+ -Binding Regulatory Domains of Mammalian NCX Isoform/Splice Variants
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    Chapter 4 The Endoplasmic Reticulum and the Cellular Reticular Network
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    Chapter 5 Structure-Function Relationship of the SERCA Pump and Its Regulation by Phospholamban and Sarcolipin
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    Chapter 6 Structural Insights into IP 3 R Function
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    Chapter 7 IP 3 Receptor Properties and Function at Membrane Contact Sites
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    Chapter 8 Structural Details of the Ryanodine Receptor Calcium Release Channel and Its Gating Mechanism
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    Chapter 9 Store-Operated Calcium Entry: An Historical Overview
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    Chapter 10 From Stores to Sinks: Structural Mechanisms of Cytosolic Calcium Regulation
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    Chapter 11 Assembly of ER-PM Junctions: A Critical Determinant in the Regulation of SOCE and TRPC1
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    Chapter 12 Beyond Intracellular Signaling: The Ins and Outs of Second Messengers Microdomains
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    Chapter 13 Mitochondrial VDAC, the Na + /Ca 2+ Exchanger, and the Ca 2+ Uniporter in Ca 2+ Dynamics and Signaling
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    Chapter 14 Annexins: Ca 2+ Effectors Determining Membrane Trafficking in the Late Endocytic Compartment
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    Chapter 15 Ca 2+ Signalling and Membrane Dynamics During Cytokinesis in Animal Cells
Attention for Chapter 11: Assembly of ER-PM Junctions: A Critical Determinant in the Regulation of SOCE and TRPC1
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Chapter title
Assembly of ER-PM Junctions: A Critical Determinant in the Regulation of SOCE and TRPC1
Chapter number 11
Book title
Membrane Dynamics and Calcium Signaling
Published in
Advances in experimental medicine and biology, January 2017
DOI 10.1007/978-3-319-55858-5_11
Pubmed ID
Book ISBNs
978-3-31-955857-8, 978-3-31-955858-5
Authors

Krishna P. Subedi, Hwei Ling Ong, Indu S. Ambudkar, Subedi, Krishna P., Ong, Hwei Ling, Ambudkar, Indu S.

Abstract

Store-operated calcium entry (SOCE), a unique plasma membrane Ca2+ entry mechanism, is activated when ER-[Ca2+] is decreased. SOCE is mediated via the primary channel, Orai1, as well as others such as TRPC1. STIM1 and STIM2 are ER-Ca2+ sensor proteins that regulate Orai1 and TRPC1. SOCE requires assembly of STIM proteins with the plasma membrane channels which occurs within distinct regions in the cell that have been termed as endoplasmic reticulum (ER)-plasma membrane (PM) junctions. The PM and ER are in close proximity to each other within this region, which allows STIM1 in the ER to interact with and activate either Orai1 or TRPC1 in the plasma membrane. Activation and regulation of SOCE involves dynamic assembly of various components that are involved in mediating Ca2+ entry as well as those that determine the formation and stabilization of the junctions. These components include proteins in the cytosol, ER and PM, as well as lipids in the PM. Recent studies have also suggested that SOCE and its components are compartmentalized within ER-PM junctions and that this process might require remodeling of the plasma membrane lipids and reorganization of structural and scaffolding proteins. Such compartmentalization leads to the generation of spatially- and temporally-controlled Ca2+signals that are critical for regulating many downstream cellular functions.

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X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Professor 2 20%
Student > Ph. D. Student 2 20%
Researcher 2 20%
Student > Master 1 10%
Unknown 3 30%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 20%
Agricultural and Biological Sciences 1 10%
Neuroscience 1 10%
Materials Science 1 10%
Engineering 1 10%
Other 0 0%
Unknown 4 40%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 15 August 2018.
All research outputs
#15,542,250
of 23,098,660 outputs
Outputs from Advances in experimental medicine and biology
#2,528
of 4,976 outputs
Outputs of similar age
#257,769
of 421,638 outputs
Outputs of similar age from Advances in experimental medicine and biology
#235
of 490 outputs
Altmetric has tracked 23,098,660 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 4,976 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.2. This one is in the 37th percentile – i.e., 37% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 421,638 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 30th percentile – i.e., 30% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 490 others from the same source and published within six weeks on either side of this one. This one is in the 36th percentile – i.e., 36% of its contemporaries scored the same or lower than it.