Evidence map›Paper›PMID 25084350›Full record

ArticlePloS one2014

A fluorescent protein scaffold for presenting structurally constrained peptides provides an effective screening system to identify high affinity target-binding peptides.

Tetsuya Kadonosono, Etsuri Yabe, Tadaomi Furuta, Akihiro Yamano, Takuya Tsubaki, Takuya Sekine, Takahiro Kuchimaru, Minoru Sakurai, Shinae Kizaka-Kondoh

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Integrin-Targeting Fluorescent Proteins: Exploration of RGD Insertion Sites.Chembiochem : a European journal of chemical biology · 2017
    Article
  6. 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.

Tetsuya KadonosonoGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama City, Japan.
Etsuri YabeGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama City, Japan.
Tadaomi FurutaCenter for Biological Resources and Informatics, Tokyo Institute of Technology, Yokohama City, Japan.
Akihiro YamanoGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama City, Japan.
Takuya TsubakiGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama City, Japan.
Takuya SekineGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama City, Japan.
Takahiro KuchimaruGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama City, Japan.
Minoru SakuraiCenter for Biological Resources and Informatics, Tokyo Institute of Technology, Yokohama City, Japan.
Shinae Kizaka-KondohGraduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama City, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peptides that have high affinity for target molecules on the surface of cancer cells are crucial for the development of targeted cancer therapies. However, unstructured peptides often fail to bind their target molecules with high affinity. To efficiently identify high-affinity target-binding peptides, we have constructed a fluorescent protein scaffold, designated gFPS, in which structurally constrained peptides are integrated at residues K131-L137 of superfolder green fluorescent protein. Molecular dynamics simulation supported the suitability of this site for presentation of exogenous peptides with a constrained structure. gFPS can present 4 to 12 exogenous amino acids without a loss of fluorescence. When gFPSs presenting human epidermal growth factor receptor type 2 (HER2)-targeting peptides were added to the culture medium of HER2-expressing cells, we could easily identify the peptides with high HER2-affinity and -specificity based on gFPS fluorescence. In addition, gFPS could be expressed on the yeast cell surface and applied for a high-throughput screening. These results demonstrate that gFPS has the potential to serve as a powerful tool to improve screening of structurally constrained peptides that have a high target affinity, and suggest that it could expedite the one-step identification of clinically applicable cancer cell-binding peptides.

Indexed as

Protein Interaction MappingRecombinant Fusion ProteinsAmino Acid SequenceCarrier ProteinsCell Surface Display TechniquesErb-b2 Receptor Tyrosine KinasesGreen Fluorescent ProteinsHumansModels, MolecularMutationNeoplasmsPeptidesProtein BindingProtein ConformationCarrier ProteinsErb-b2 Receptor Tyrosine KinasesGreen Fluorescent ProteinsPeptidesRecombinant Fusion Proteins

Identifiers

PMID25084350
PMCPMC4118881

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.