Evidence map›Paper›PMID 26264666›Full record

ArticleNucleic acids research2016

DNA binding fluorescent proteins for the direct visualization of large DNA molecules.

Seonghyun Lee, Yeeun Oh, Jungyoon Lee, Sojeong Choe, Sangyong Lim, Hyun Soo Lee, Kyubong Jo, David C Schwartz

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-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

13 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  7. 21 Fluorescent Protein-Based DNA Staining Dyes.Molecules (Basel, Switzerland) · 2022
    Article
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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

8 authors at 2 institutions in 2 countries.

Seonghyun LeeDepartment of Chemistry and Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsudong, Mapogu, Seoul, 121-742, Korea.
Yeeun OhDepartment of Chemistry and Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsudong, Mapogu, Seoul, 121-742, Korea.
Jungyoon LeeDepartment of Chemistry and Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsudong, Mapogu, Seoul, 121-742, Korea.
Sojeong ChoeDepartment of Chemistry and Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsudong, Mapogu, Seoul, 121-742, Korea.
Sangyong LimResearch Division for Biotechnology, Korea Atomic Energy Research Institute, Jeongeup 580-185, Korea.
Hyun Soo LeeDepartment of Chemistry and Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsudong, Mapogu, Seoul, 121-742, Korea.
Kyubong JoDepartment of Chemistry and Interdisciplinary Program of Integrated Biotechnology, Sogang University, 1 Shinsudong, Mapogu, Seoul, 121-742, Korea jokyubong@sogang.ac.kr.
David C SchwartzLaboratory for Molecular and Computational Genomics, Department of Chemistry, Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI 53705, USA.
Korea Atomic Energy Research Institute · KRUniversity of Wisconsin–Madison · US

Funding

NEW PHYSICAL METHODOLOGIES FOR GENOMIC ANALYSISR01HG000225 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI SCHWARTZ, DAVID C. · 1991 to 2014
$5.2M
Single Molecule Genome Analysis of OligodendrogliomaR33CA111933 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SCHWARTZ, DAVID C. · 2005 to 2007
$1.2M
Scalable Cancer Genomics via Nanocoding and SequencingR33CA182360 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI MA, JIAN, SCHWARTZ, DAVID C. · 2015 to 2017
$1.1M
NCI NIH HHS R33 CA111933NCI NIH HHS R33 CA182360NHGRI NIH HHS 5R01HG000225NHGRI NIH HHS R01 HG000225
6 · The paper itself

Abstract

Fluorescent proteins that also bind DNA molecules are useful reagents for a broad range of biological applications because they can be optically localized and tracked within cells, or provide versatile labels for in vitro experiments. We report a novel design for a fluorescent, DNA-binding protein (FP-DBP) that completely 'paints' entire DNA molecules, whereby sequence-independent DNA binding is accomplished by linking a fluorescent protein to two small peptides (KWKWKKA) using lysine for binding to the DNA phosphates, and tryptophan for intercalating between DNA bases. Importantly, this ubiquitous binding motif enables fluorescent proteins (Kd = 14.7 μM) to confluently stain DNA molecules and such binding is reversible via pH shifts. These proteins offer useful robust advantages for single DNA molecule studies: lack of fluorophore mediated photocleavage and staining that does not perturb polymer contour lengths. Accordingly, we demonstrate confluent staining of naked DNA molecules presented within microfluidic devices, or localized within live bacterial cells.

Indexed as

Molecular ImagingRecombinant Fusion ProteinsDNADNA-Binding ProteinsEscherichia coliHumansLuminescent ProteinsMicroscopy, FluorescenceDNADNA-Binding ProteinsLuminescent ProteinsRecombinant Fusion Proteins

Identifiers

PMID26264666
PMCPMC4705684
OpenAlexW1786990908

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.