Evidence map›Paper›PMID 35377367›Full record

ArticleJournal of visualized experiments : JoVE2022

Förster Resonance Energy Transfer Mapping: A New Methodology to Elucidate Global Structural Features.

Jack Northrop, Donald B Oliver, Ishita Mukerji

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Integration Host Factor Binds DNA Holliday Junctions.International journal of molecular sciences · 2022
    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

3 authors.

Jack NorthropMolecular Biology and Biochemistry Department, Wesleyan University.
Donald B OliverMolecular Biology and Biochemistry Department, Wesleyan University; Molecular Biophysics Program, Wesleyan University.
Ishita MukerjiMolecular Biology and Biochemistry Department, Wesleyan University; Molecular Biophysics Program, Wesleyan University; imukerji@wesleyan.edu.

Funding

Investigating the Role of MutSy in Meiotic Recombination and Maintaining Genome IntegrityR15GM135904 · NIGMS · WESLEYAN UNIVERSITY · PI MUKERJI, ISHITA · 2019 to 2019
$493k
Mechanism of SecA-dependent protein translocationR15GM110552 · NIGMS · WESLEYAN UNIVERSITY · PI OLIVER, DONALD B. · 2014 to 2014
$374k
NIGMS NIH HHS R15 GM110552NIGMS NIH HHS R15 GM135904
6 · The paper itself

Abstract

Förster resonance energy transfer (FRET) is an established fluorescence-based method used to successfully measure distances in and between biomolecules in vitro as well as within cells. In FRET, the efficiency of energy transfer, measured by changes in fluorescence intensity or lifetime, relates to the distance between two fluorescent molecules or labels. Determination of dynamics and conformational changes from the distances are just some examples of applications of this method to biological systems. Under certain conditions, this methodology can add to and enhance existing X-ray crystal structures by providing information regarding dynamics, flexibility, and adaptation to binding surfaces. We describe the use of FRET and associated distance determinations to elucidate structural properties, through the identification of a binding site or the orientations of dimer subunits. Through judicious choice of labeling sites, and often employment of multiple labeling strategies, we have successfully applied these mapping methods to determine global structural properties in a protein-DNA complex and the SecA-SecYEG protein translocation system. In the SecA-SecYEG system, we have used FRET mapping methods to identify the preprotein-binding site and determine the local conformation of the bound signal sequence region. This study outlines the steps for performing FRET mapping studies, including identification of appropriate labeling sites, discussion of possible labels including non-native amino acid residues, labeling procedures, how to perform measurements, and interpreting the data.

Indexed as

Fluorescence Resonance Energy TransferProtein Sorting SignalsBinding SitesProtein BindingProtein Sorting Signals

Identifiers

PMID35377367
PMCPMC10639101

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.