Evidence map›Paper›PMID 26322679›Full record

ArticleNature cell biology2015

Proteomic mapping of ER-PM junctions identifies STIMATE as a regulator of Ca²⁺ influx.

Ji Jing, Lian He, Aomin Sun, Ariel Quintana, Yuehe Ding, Guolin Ma, Peng Tan, Xiaowen Liang, Xiaolu Zheng, Liangyi Chen and 9 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 1 pooled it
12.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

118 citing papers in PubMed, 1 synthesis or guideline pooled it, 206 citations in OpenAlex.

  1. Stay in touch with the endoplasmic reticulum.Science China. Life sciences · 2024
    Pooled it
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  18. STIM1 and lipid interactions at ER-PM contact sites.American journal of physiology. Cell physiology · 2025
    Review
  19. Article
  20. Article

58 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 7 institutions in 2 countries.

Ji JingInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Lian HeInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Aomin SunBeijing Key Laboratory of Gene Resource and Molecular Development, College of Life Sciences, Beijing Normal University, Beijing 100875, China.
Ariel QuintanaDivision of Signaling and Gene Expression, La Jolla Institute for Allergy and Immunology, La Jolla, California 92037, USA.
Yuehe DingNational Institute of Biological Sciences, Beijing 102206, China.
Guolin MaInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Peng TanInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Xiaowen LiangInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Xiaolu ZhengInstitute of Molecular Medicine, Peking University, Beijing 100871, China.
Liangyi ChenInstitute of Molecular Medicine, Peking University, Beijing 100871, China.
Xiaodong ShiDepartment of Chemistry, West Virginia University, Morgantown, West Virginia 26506, USA.
Shenyuan L ZhangDepartment of Medical Physiology, College of Medicine, Texas A&M University Health Science Center, Temple, Texas 76504, USA.
Ling ZhongInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Yun HuangInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Meng-Qiu DongNational Institute of Biological Sciences, Beijing 102206, China.
Cheryl L WalkerInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Patrick G HoganDivision of Signaling and Gene Expression, La Jolla Institute for Allergy and Immunology, La Jolla, California 92037, USA.
Youjun WangBeijing Key Laboratory of Gene Resource and Molecular Development, College of Life Sciences, Beijing Normal University, Beijing 100875, China.
Yubin ZhouInstitute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas 77030, USA.
Texas A&M University · USTexas A&M Health Science Center · USBeijing Normal University · CNLa Jolla Institute for Immunology · USNational Institute of Biological Sciences, Beijing · CNPeking University · CNWest Virginia University · US

Funding

STIM-ORAI signaling and other calcium influx pathways in lymphocytesR01AI084167 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI HOGAN, PATRICK · 2009 to 2019
$4.9M
Tumor Suppressor Localization and Function at the PeroxisomeR01CA143811 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WALKER, CHERYL L. · 2010 to 2018
$2.9M
MOLECULAR CONTROL OF CALCIUM INFLUX AT THE ER-PLASMA MEMBRANE JUNCTIONSR01GM112003 · NIGMS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ZHOU, YUBIN · 2014 to 2022
$2.7M
Nanoscale regulation of store-operated calcium entry through STIM-ORAI signallingR01GM110397 · NIGMS · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI HOGAN, PATRICK, LILLEMEIER, BJOERN F · 2014 to 2017
$1.4M
NCI NIH HHS R01 CA143811NIAID NIH HHS R01 AI084167NIGMS NIH HHS R01 GM110397NIGMS NIH HHS R01 GM112003
6 · The paper itself

Abstract

Specialized junctional sites that connect the plasma membrane (PM) and endoplasmic reticulum (ER) play critical roles in controlling lipid metabolism and Ca(2+) signalling. Store-operated Ca(2+) entry mediated by dynamic STIM1-ORAI1 coupling represents a classical molecular event occurring at ER-PM junctions, but the protein composition and how previously unrecognized protein regulators facilitate this process remain ill-defined. Using a combination of spatially restricted biotin labelling in situ coupled with mass spectrometry and a secondary screen based on bimolecular fluorescence complementation, we mapped the proteome of intact ER-PM junctions in living cells without disrupting their architectural integrity. Our approaches led to the discovery of an ER-resident multi-transmembrane protein that we call STIMATE (STIM-activating enhancer, encoded by TMEM110) as a positive regulator of Ca(2+) influx in vertebrates. STIMATE physically interacts with STIM1 to promote STIM1 conformational switch. Genetic depletion of STIMATE substantially reduces STIM1 puncta formation at ER-PM junctions and suppresses the Ca(2+)-NFAT signalling. Our findings enable further genetic studies to elucidate the function of STIMATE in normal physiology and disease, and set the stage to uncover more uncharted functions of hitherto underexplored ER-PM junctions.

Indexed as

Amino Acid SequenceAnimalsBase SequenceBiological TransportCalciumCell MembraneChlorocebus aethiopsCOS CellsEndoplasmic ReticulumGene Expression ProfilingGene SilencingHEK293 CellsHeLa CellsHumansMembrane ProteinsMicroscopy, ConfocalCalciumMembrane ProteinsNeoplasm ProteinsProteomeSTIM1 protein, humanSTIMATE protein, humanStromal Interaction Molecule 1

Identifiers

PMID26322679
PMCPMC4589512
OpenAlexW2210163512

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.