Evidence map›Paper›PMID 36936069›Full record

ArticleCell reports methods2023

A FRET sensor for the real-time detection of long chain acyl-CoAs and synthetic ABHD5 ligands.

Emilio P Mottillo, Ljiljana Mladenovic-Lucas, Huamei Zhang, Li Zhou, Christopher V Kelly, Pablo A Ortiz, James G Granneman

Open access · goldAbstract read
In one paragraph

Article in Cell reports methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Dynamic sampling fromLab on a chip · 2024
    Article
  4. Article
  5. Review
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

7 authors at 2 institutions in 1 country.

Emilio P MottilloHypertension and Vascular Research Division, Department of Internal Medicine, Henry Ford Hospital, 6135 Woodward Avenue, Detroit, MI 48202, USA.
Ljiljana Mladenovic-LucasCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48202, USA.
Huamei ZhangCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48202, USA.
Li ZhouCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48202, USA.
Christopher V KellyDepartment of Physics and Astronomy, Wayne State University, Detroit, MI 48202, USA.
Pablo A OrtizHypertension and Vascular Research Division, Department of Internal Medicine, Henry Ford Hospital, 6135 Woodward Avenue, Detroit, MI 48202, USA.
James G GrannemanCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48202, USA.
Wayne State University · USHenry Ford Hospital · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Analysis of Lipolytic Trafficking in Adipocytes.R01DK076629 · NIDDK · WAYNE STATE UNIVERSITY · PI James G Granneman, Christopher V Kelly · 2009 to 2026
$7.1M
Preclinical validation of ABHD5 as a target for treatment of obesity.R01DK105963 · NIDDK · WAYNE STATE UNIVERSITY · PI GRANNEMAN, JAMES G · 2015 to 2018
$2.7M
Molecular and cellular analysis of the ABHD5/PNPLA3 metabolon in lipid homeostasisR01DK126743 · NIDDK · WAYNE STATE UNIVERSITY · PI MOTTILLO, EMILIO · 2021 to 2025
$2.4M
Direct analysis of lipolysis-mediated signaling eventsR00DK114471 · NIDDK · WAYNE STATE UNIVERSITY · PI MOTTILLO, EMILIO · 2019 to 2021
$747k
A genetically-encoded sensor for imaging intracellular fatty acidsR21DK091741 · NIDDK · WAYNE STATE UNIVERSITY · PI GRANNEMAN, JAMES G · 2011 to 2012
$418k
NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R00 DK114471NIDDK NIH HHS R01 DK076629NIDDK NIH HHS R01 DK105963NIDDK NIH HHS R01 DK126743NIDDK NIH HHS R21 DK091741
6 · The paper itself

Abstract

Intracellular long-chain acyl-coenzyme As (LC-acyl-CoAs) are thought to be under tight spatial and temporal controls, yet the ability to image LC-acyl-CoAs in live cells is lacking. Here, we developed a fluorescence resonance energy transfer (FRET) sensor for LC-acyl-CoAs based on the allosterically regulated interaction between α/β hydrolase domain-containing 5 (ABHD5) and Perilipin 5. The genetically encoded sensor rapidly detects intracellular LC-acyl-CoAs generated from exogenous and endogenous fatty acids (FAs), as well as synthetic ABHD5 ligands. Stimulation of lipolysis in brown adipocytes elevated intracellular LC-acyl-CoAs in a cyclic fashion, which was eliminated by inhibiting PNPLA2 (ATGL), the major triglyceride lipase. Interestingly, inhibition of LC-acyl-CoA transport into mitochondria elevated intracellular LC-acyl-CoAs and dampened their cycling. Together, these observations reveal an intimate feedback control between LC-acyl-CoA generation from lipolysis and utilization in mitochondria. We anticipate that this sensor will be an important tool to dissect intracellular LC-acyl-CoA dynamics as well to discover novel synthetic ABHD5 ligands.

Indexed as

Acyl Coenzyme AFluorescence Resonance Energy TransferFatty AcidsLipaseLipolysisAcyl Coenzyme AFatty AcidsLipaseadipose triglyceride lipaseCGI-58fatty acidsgenetically encoded FRET sensorlipid dropletlong-chain acyl-CoAsmitochondriaPerilipinreal-time monitoringα/β hydrolase domain-containing 5

Identifiers

PMID36936069
PMCPMC10014278
OpenAlexW4317940480

What OpenQuestion 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 OpenQuestion graph.