Evidence map›Paper›PMID 30287690›Full record

ArticleThe Journal of biological chemistry2018

Scrambling of natural and fluorescently tagged phosphatidylinositol by reconstituted G protein-coupled receptor and TMEM16 scramblases.

Lei Wang, Yugo Iwasaki, Kiran K Andra, Kalpana Pandey, Anant K Menon, Peter Bütikofer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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  8. Review
  9. Genome-wide CRISPR screen reveals CLPTM1L as a lipid scramblase required for efficient glycosylphosphatidylinositol biosynthesis.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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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

6 authors at 4 institutions in 4 countries.

Lei WangFrom the Institute of Biochemistry and Molecular Medicine and; Graduate School for Cellular and Biochemical Sciences, University of Bern, 3012 Bern, Switzerland.
Yugo Iwasakithe Laboratory of Molecular Biotechnology, Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho, Nagoya 464-8601, Japan, and.
Kiran K Andrathe Department of Biochemistry, Weill Cornell Medical College, New York, New York 10065.
Kalpana Pandeythe Department of Biochemistry, Weill Cornell Medical College, New York, New York 10065.
Anant K Menonthe Department of Biochemistry, Weill Cornell Medical College, New York, New York 10065. Electronic address: akm2003@med.cornell.edu.
Peter BütikoferFrom the Institute of Biochemistry and Molecular Medicine and. Electronic address: peter.buetikofer@ibmm.unibe.ch.
Cornell University · USNagoya University · JPUniversidad Iberoamericana · DOUniversity of Bern · CH

Funding

Ca2+-dependent lipid scrambling and ion transport by TMEM16 proteinsR01GM106717 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI ACCARDI, ALESSIO, WEINSTEIN, HAREL · 2014 to 2023
$4.3M
Molecular mechanism of phospholipid scrambling by rhodopsinR21EY028314 · NEI · WEILL MEDICAL COLL OF CORNELL UNIV · PI KHELASHVILI, GEORGE, MENON, ANANT K · 2017 to 2018
$466k
NEI NIH HHS R21 EY028314NIGMS NIH HHS R01 GM106717
6 · The paper itself

Abstract

Members of the G protein-coupled receptor and TMEM16 (transmembrane protein 16) protein families are phospholipid scramblases that facilitate rapid, bidirectional movement of phospholipids across a membrane bilayer in an ATP-independent manner. On reconstitution into large unilamellar vesicles, these proteins scramble more than 10,000 lipids/protein/s as measured with co-reconstituted fluorescent nitrobenzoxadiazole (NBD)-labeled phospholipids. Although NBD-labeled phospholipids are ubiquitously used as reporters of scramblase activity, it remains unclear whether the NBD modification influences the quantitative outcomes of the scramblase assay. We now report a refined biochemical approach for measuring the activity of scramblase proteins with radiolabeled natural phosphatidylinositol ([

Indexed as

AnimalsAnoctaminsBiological TransportCattleFluorescenceFungal ProteinsHydrolysisKineticsNectriaOpsinsPhosphatidylinositolsPhospholipid Transfer ProteinsType C PhospholipasesAnoctaminsFungal ProteinsOpsinsPhosphatidylinositolsPhospholipid Transfer ProteinsType C PhospholipasesglycerophospholipidG protein–coupled receptor (GPCR)liposomemembrane transportphosphatidylinositolPhospholipase CscramblaseTMEM16

Identifiers

PMID30287690
PMCPMC6254352
OpenAlexW2895666882

What OpenQuestion holds

Textmetadata
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.