Evidence map›Paper›PMID 25906065›Full record

ArticlePloS one2015

LucY: A Versatile New Fluorescent Reporter Protein.

Michele E Auldridge, Hongnan Cao, Saurabh Sen, Laura P Franz, Craig A Bingman, Ragothaman M Yennamalli, George N Phillips, David Mead, Eric J Steinmetz

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
0.4field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Overview of the reporter genes and reporter mouse models.Animal models and experimental medicine · 2018
    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

9 authors at 3 institutions in 1 country.

Michele E AuldridgeLucigen Corp., Middleton, WI, United States of America.
Hongnan CaoDepartment of Biochemistry and Cell Biology, Rice University, Houston, Texas, United States of America.
Saurabh SenLucigen Corp., Middleton, WI, United States of America.
Laura P FranzLucigen Corp., Middleton, WI, United States of America.
Craig A BingmanDepartment of Biochemistry, University of Wisconsin, Madison, WI, United States of America.
Ragothaman M YennamalliDepartment of Biochemistry and Cell Biology, Rice University, Houston, Texas, United States of America.
George N PhillipsDepartment of Biochemistry and Cell Biology, Rice University, Houston, Texas, United States of America; Department of Biochemistry, University of Wisconsin, Madison, WI, United States of America.
David MeadLucigen Corp., Middleton, WI, United States of America.
Eric J SteinmetzLucigen Corp., Middleton, WI, United States of America.
Lucigen Corporation · USRice University · USUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report on the discovery, isolation, and use of a novel yellow fluorescent protein. Lucigen Yellow (LucY) binds one FAD molecule within its core, thus shielding it from water and maintaining its structure so that fluorescence is 10-fold higher than freely soluble FAD. LucY displays excitation and emission spectra characteristic of FAD, with 3 excitation peaks at 276 nm, 377 nm, and 460 nm and a single emission peak at 530 nm. These excitation and emission maxima provide the large Stokes shift beneficial to fluorescence experimentation. LucY belongs to the MurB family of UDP-N-acetylenolpyruvylglucosamine reductases. The high resolution crystal structure shows that in contrast to other structurally resolved MurB enzymes, LucY does not contain a potentially quenching aromatic residue near the FAD isoalloxazine ring, which may explain its increased fluorescence over related proteins. Using E. coli as a system in which to develop LucY as a reporter, we show that it is amenable to circular permutation and use as a reporter of protein-protein interaction. Fragmentation between its distinct domains renders LucY non-fluorescent, but fluorescence can be partially restored by fusion of the fragments to interacting protein domains. Thus, LucY may find application in Protein-fragment Complementation Assays for evaluating protein-protein interactions.

Indexed as

Bacterial ProteinsCrystallography, X-RayEscherichia coliFlavin-Adenine DinucleotideGenes, ReporterLuminescent ProteinsProtein Interaction Domains and MotifsProtein Structure, TertiaryRecombinant ProteinsSpectrometry, FluorescenceBacterial ProteinsFlavin-Adenine DinucleotideLuminescent ProteinsRecombinant Proteinsyellow fluorescent protein, Bacteria

Identifiers

PMID25906065
PMCPMC4408115
OpenAlexW2066556257

What OpenQuestion holds

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LicenceCC BY
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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.