Evidence map›Paper›PMID 38761168›Full record

ArticleThe Plant journal : for cell and molecular biology2024

In planta imaging of pyridine nucleotides using second-generation fluorescent protein biosensors.

Shey-Li Lim, Jinhong Liu, Gilles Dupouy, Gaurav Singh, Stéphanie Baudrey, Lang Yang, Jia Yi Zhong, Marie-Edith Chabouté, Boon Leong Lim

Abstract read
In one paragraph

Article in The Plant journal : for cell and molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. A family of NADPH/NADPNature communications · 2024
    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

9 authors.

Shey-Li Lim *School of Biological Sciences, University of Hong Kong, Hong Kong, China.
Jinhong Liu *School of Biological Sciences, University of Hong Kong, Hong Kong, China.
Gilles DupouyInstitut de Biologie Moléculaire des Plantes, CNRS, Université de Strasbourg, Strasbourg, 67084, France.
Gaurav SinghInstitut de Biologie Moléculaire des Plantes, CNRS, Université de Strasbourg, Strasbourg, 67084, France.
Stéphanie BaudreyArchitecture et Réactivité de l'ARN, Université de Strasbourg, CNRS, UPR 9002, Strasbourg, 67000, France.
Lang YangSchool of Biological Sciences, University of Hong Kong, Hong Kong, China.
Jia Yi ZhongSchool of Biological Sciences, University of Hong Kong, Hong Kong, China.
Marie-Edith ChaboutéInstitut de Biologie Moléculaire des Plantes, CNRS, Université de Strasbourg, Strasbourg, 67084, France.ORCID 0000-0001-8688-721X
Boon Leong LimSchool of Biological Sciences, University of Hong Kong, Hong Kong, China.ORCID 0000-0002-2720-2353

Funding

Agence Nationale de la Recherche ANR-20-CE13-0025Area of Excellence Scheme AoE/M-403/16Centre National de la Recherche Scientifique CNRS (10.13039/501100004794)Hong Kong Research Grants Council General Research Fund 17102322Hong Kong Research Grants Council General Research Fund 17103921Hong Kong RGC Postdoctoral Fellowship Scheme PDFS2324-7S01Human Frontier Science Program HFSP-RGP 0009/2018Innovation and Technology Fund (Funding Support to State Key Laboratory of Agrobiotechnology)National Natural Science Foundation of China 31870212National Natural Science Foundation of China 32070394
6 · The paper itself

Abstract

Redox changes of pyridine nucleotides in cellular compartments are highly dynamic and their equilibria are under the influence of various reducing and oxidizing reactions. To obtain spatiotemporal data on pyridine nucleotides in living plant cells, typical biochemical approaches require cell destruction. To date, genetically encoded fluorescent biosensors are considered to be the best option to bridge the existing technology gap, as they provide a fast, accurate, and real-time readout. However, the existing pyridine nucleotides genetically encoded fluorescent biosensors are either sensitive to pH change or slow in dissociation rate. Herein, we employed the biosensors which generate readouts that are pH stable for in planta measurement of NADH/NAD

Indexed as

ArabidopsisBiosensing TechniquesNADNADPPlants, Genetically ModifiedCytosolHydrogen-Ion ConcentrationLuminescent ProteinsOxidation-ReductionPlastidsPollen TubeLuminescent ProteinsNADNADPNADHNADPHplastidpollen tuberatiometric biosensorredoxroot hairtechnical advance

Identifiers

PMID38761168
PMCPMC13087476

What OpenQuestion holds

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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.