Evidence map›Paper›PMID 35741049›Full record

ReviewCells2022

Genetically Encoded ATP Biosensors for Direct Monitoring of Cellular ATP Dynamics.

Donnell White, Qinglin Yang

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Intracellular MgFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  13. Review
  14. Article
  15. iATPSnFR2: A high-dynamic-range fluorescent sensor for monitoring intracellular ATP.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Application of the LuminescentFoods (Basel, Switzerland) · 2023
    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

2 authors at 1 institution in 1 country.

Donnell WhiteCardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.ORCID 0000-0002-5368-3752
Qinglin YangCardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.
Louisiana State University Health Sciences Center New Orleans · US

Funding

Improving Mitochondrial Function to Protect against Myocardial Ischemia/ReperfusionR01HL135336 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YANG, QINGLIN · 2017 to 2020
$1.5M
Restore Energy Capacity in the Aging HeartR03AG055899 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YANG, QINGLIN · 2017 to 2018
$149k
NHLBI NIH HHS R01 HL135336NIA NIH HHS R03 AG055899
6 · The paper itself

Abstract

Adenosine 5'-triphosphate, or ATP, is the primary molecule for storing and transferring energy in cells. ATP is mainly produced via oxidative phosphorylation in mitochondria, and to a lesser extent, via glycolysis in the cytosol. In general, cytosolic glycolysis is the primary ATP producer in proliferative cells or cells subjected to hypoxia. On the other hand, mitochondria produce over 90% of cellular ATP in differentiated cells under normoxic conditions. Under pathological conditions, ATP demand rises to meet the needs of biosynthesis for cellular repair, signaling transduction for stress responses, and biochemical processes. These changes affect how mitochondria and cytosolic glycolysis function and communicate. Mitochondria undergo remodeling to adapt to the imbalanced demand and supply of ATP. Otherwise, a severe ATP deficit will impair cellular function and eventually cause cell death. It is suggested that ATP from different cellular compartments can dynamically communicate and coordinate to adapt to the needs in each cellular compartment. Thus, a better understanding of ATP dynamics is crucial to revealing the differences in cellular metabolic processes across various cell types and conditions. This requires innovative methodologies to record real-time spatiotemporal ATP changes in subcellular regions of living cells. Over the recent decades, numerous methods have been developed and utilized to accomplish this task. However, this is not an easy feat. This review evaluates innovative genetically encoded biosensors available for visualizing ATP in living cells, their potential use in the setting of human disease, and identifies where we could improve and expand our abilities.

Indexed as

Biosensing TechniquesOxidative PhosphorylationAdenosine TriphosphateGlycolysisHumansMitochondriaAdenosine TriphosphateATPATP dynamicscellular bioenergeticsenergy metabolismgenetically encoded fluorescent biosensorsglycolysismitochondriareal-time ATP monitorspatiotemporal

Identifiers

PMID35741049
PMCPMC9221525
OpenAlexW4282924206

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.