Evidence map›Paper›PMID 28572662›Full record

ArticleScientific reports2017

Discovery of a polystyrene binding peptide isolated from phage display library and its application in peptide immobilization.

Xu Qiang, Keyong Sun, Lijun Xing, Yifeng Xu, Hong Wang, Zhengpin Zhou, Juan Zhang, Fang Zhang, Bilgen Caliskan, Min Wang and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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  9. Production of high-affinity glycosylated anti-mouse conjugated nanobodies inFrontiers in bioengineering and biotechnology · 2025
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  12. Modular Design for Proteins Assembling into Antifouling Coatings: Case of Gold Surfaces.Langmuir : the ACS journal of surfaces and colloids · 2023
    Article
  13. Review
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  15. Article
  16. 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

11 authors.

Xu QiangSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Keyong SunSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Lijun XingSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Yifeng XuSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Hong WangSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Zhengpin ZhouSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Juan ZhangSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Fang ZhangJiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, P.R. China.
Bilgen CaliskanSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Min WangSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China. minwang@cpu.edu.cn.
Zheng QiuSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, 210009, P.R. China. qiuzheng@cpu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phage peptide display is a powerful technique for discovery of various target-specific ligands. However, target-unrelated peptides can often be obtained and cause ambiguous results. Peptide PB-TUP has been isolated repeatedly in our laboratory on different targets and we conducted a research on PB-TUP phage to investigate their binding properties and rate of propagation. ELISA and phage recovery assay demonstrated that PB-TUP phage had a significant superior affinity to polystyrene solid surface compared with control phage clones. In this study, some incidental bindings are excluded like blocking agents and non-specific binding of secondary antibodies. Propagation rate assays of the selected phage clones showed that the growth rate of PB-TUP phage was not superior to the control phages. Furthermore, the binding of PB-TUB to polystyrene was concentration dependent and varied with solution pH. Molecular modeling revealed that stable structures of α-helix and β-turn may contribute to the binding of PB-TUP to polystyrene plate. The PB-TUP sequence was fused to the N-terminus of peptide P2 and the fusion peptide significantly increased the binding affinity to polystyrene. The fusion peptide also enhanced the cell adhesion ability of peptide P2 with human umbilical vein endothelial cell (HUVEC). The addition of the polystyrene binding peptide provided a convenient method for peptide immobilization.

Indexed as

BacteriophagesCells, CulturedCell Surface Display TechniquesHumansModels, MolecularPeptide LibraryPeptidesPolystyrenesPeptide LibraryPeptidesPolystyrenes

Identifiers

PMID28572662
PMCPMC5453990

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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.