Evidence map›Paper›PMID 28595602›Full record

ArticleBMC genomics2017

Assembly and use of high-density recombinant peptide chips for large-scale ligand screening is a practical alternative to synthetic peptide libraries.

Harald Hundsberger, Kamil Önder, Peter Schuller-Götzburg, Dezso P Virok, Julia Herzog, Raphaela Rid

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Article in BMC genomics, 2017. 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

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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

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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.

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4 · The record

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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

6 authors.

Harald HundsbergerDepartment of Medical and Pharmaceutical Biotechnology, University of Applied Sciences, 3500, Krems, Austria.
Kamil ÖnderResearch Program for Rational Drug Design in Dermatology and Rheumatology, Department of Dermatology, Paracelsus Medical University of Salzburg, 5020, Salzburg, Austria. oender@procomcure.com.
Peter Schuller-GötzburgResearch Program in Prosthetics, Biomechanics and Biomaterials, Paracelsus Private Medical University, 5020, Salzburg, Austria.
Dezso P VirokDepartment of Medicinal Microbiology and Immunobiology, University of Szeged, Szeged, 6722, Hungary.
Julia HerzogResearch Program for Rational Drug Design in Dermatology and Rheumatology, Department of Dermatology, Paracelsus Medical University of Salzburg, 5020, Salzburg, Austria.
Raphaela RidResearch Program for Rational Drug Design in Dermatology and Rheumatology, Department of Dermatology, Paracelsus Medical University of Salzburg, 5020, Salzburg, Austria.ORCID 0000-0003-2937-7226

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecombinant peptide chips could constitute a versatile complementation to state-of-the-art in situ (chemical on-chip) synthesis, particle-based printing, or pre-manufactured peptide spotting. Bottlenecks still impeding a routine implementation - from restricted peptide lengths, low diversity and low array densities to high costs - could so be overcome.

methodsTo assess overall performance, we assembled recombinant chips composed of 38,400 individual peptide spots on the area of a standard 96-well microtiter plate from comprehensive, highly diverse (>107 single clones) short random peptide libraries.

resultsScreening of altogether 476,160 clones against Streptavidin uncovered 2 discrete new binders: a characteristic HPQ-motif containing VSHPQAPF and a cyclic CSGSYGSC peptide. Interactions were technically confirmed by fluorescence polarization as well as biolayer-interferometry, and their potential suitability as novel detection tags evaluated by detection of a peptide-fused exemplary test protein.

conclusionFrom our data we conclude that the presented technical pipeline can reliably identify novel hits, useful as first-generation binders or templates for subsequent ligand design plus engineering.

Indexed as

Peptide LibraryLigandsProtein Array AnalysisRecombinant ProteinsStreptavidinLigandsPeptide LibraryRecombinant ProteinsStreptavidinDiversityHigh affinityLigand designPeptide libraryPeptide screeningProtein chipProtein tagsRecombinant peptide arrayRecombinational cloningTarget binding

Identifiers

PMID28595602
PMCPMC5463365

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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.