Evidence map›Paper›PMID 34368510›Full record

ReviewJACC. Basic to translational science2021

Use of Proximity Labeling in Cardiovascular Research.

Jared Kushner, Arianne Papa, Steven O Marx

Abstract readReview
In one paragraph

Review in JACC. Basic to translational science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jared KushnerDivision of Cardiology, Department of Medicine, Columbia University, Vagelos College of Physicians and Surgeons, New York, New York, USA.
Arianne PapaDepartment of Physiology and Cellular Biophysics, Columbia University, Vagelos College of Physicians and Surgeons, New York, New York, USA.
Steven O MarxDivision of Cardiology, Department of Medicine, Columbia University, Vagelos College of Physicians and Surgeons, New York, New York, USA.

Funding

L-type channel trafficking and modulation in heartR01HL121253 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Henry M. Colecraft, Steven O Marx · 2014 to 2026
$8.4M
Exploring the Molecular Physiology of Atrial FibrillationR01HL140934 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MARKS, ANDREW ROBERT, MARX, STEVEN O · 2018 to 2025
$6.0M
Phosphorylation-dependent regulation of calcium channels by macromolecular complexesR01HL146149 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Steven O Marx, Geoffrey S Pitt · 2019 to 2026
$5.0M
Investigating Cardiac Ion Channels by Novel MethodsR01HL155377 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Steven O Marx · 2021 to 2026
$3.8M
Multidisciplinary Research Training in Cardiovascular DiseaseT32HL160520 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Geoffrey S Pitt, Jonathan W. Weinsaft · 2022 to 2026
$2.0M
Regulators and interactomes of CaV1.2 in health and diseaseK08HL151969 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KUSHNER, JARED S · 2021 to 2025
$827k
NHLBI NIH HHS K08 HL151969NHLBI NIH HHS R01 HL121253NHLBI NIH HHS R01 HL140934NHLBI NIH HHS R01 HL146149NHLBI NIH HHS R01 HL155377NHLBI NIH HHS T32 HL160520
6 · The paper itself

Abstract

Protein-protein interactions are of paramount importance in regulating normal cardiac physiology. Methodologies to elucidate these interactions in vivo have been limited. Recently, proximity-dependent biotinylation, with the use of BioID, TurboID, and ascorbate peroxidase, has been developed to uncover cellular neighborhoods and novel protein-protein interactions. These cutting-edge techniques have enabled the identification of subcellular localizations of specific proteins and the neighbors or interacting proteins within these subcellular regions. In contrast to classic methods such as affinity purification and subcellular fractionation, these techniques add covalently bound tags in living cells, such that spatial relationships and interaction networks are not disrupted. Recently, these methodologies have been used to identify novel protein-protein interactions relevant to the cardiovascular system. In this review, we discuss the development and current use of proximity biotin-labeling for cardiovascular research.

Indexed as

APEX, ascorbate peroxidaseBioID, biotin identificationcalcium channelsER, endoplasmic reticulumHEK, human embryonic kidneyHRP, horseradish peroxidaseJAM-C, junctional adhesion molecule CJph2, junctophilin 2mass spectrometryPKA, protein kinase Aprotein-protein interactionsproximity-labelingsympathetic nervous systemTMT SPS MS3, tandem mass tag triple-stage mass spectrometry

Identifiers

PMID34368510
PMCPMC8326230

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.