Evidence map›Paper›PMID 35735542›Full record

ArticleBiosensors2022

Charge-Sensitive Optical Detection of Binding Kinetics between Phage-Displayed Peptide Ligands and Protein Targets.

Runli Liang, Yingnan Zhang, Guangzhong Ma, Shaopeng Wang

Abstract read
In one paragraph

Article in Biosensors, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Runli LiangBiodesign Center for Bioelectronics and Biosensors, Arizona State University, Tempe, AZ 85287, USA.
Yingnan ZhangDepartment of Early Discovery Biochemistry, Genentech, South San Francisco, CA 94080, USA.
Guangzhong MaBiodesign Center for Bioelectronics and Biosensors, Arizona State University, Tempe, AZ 85287, USA.ORCID 0000-0002-1197-659X
Shaopeng WangBiodesign Center for Bioelectronics and Biosensors, Arizona State University, Tempe, AZ 85287, USA.ORCID 0000-0002-2680-0503

Funding

Development of a charge-sensitive optical detection system for high-throughput study of small moleculesR44GM139535 · NIGMS · BIOSENSING INSTRUMENT, INC. · PI LY, NGUYEN · 2021 to 2022
$1.7M
Charge sensitive optical detection for high-throughput study of small moleculesR33CA202834 · NCI · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI TAO, NONGJIAN · 2016 to 2018
$1.1M
Genentech Inc. CLL-016354NCI NIH HHS R33 CA202834NIGMS NIH HHS R44 GM139535NIH HHS R33CA202834, R44GM139535
6 · The paper itself

Abstract

Phage display technology has been a powerful tool in peptide drug development. However, the supremacy of phage display-based peptide drug discovery is plagued by the follow-up process of peptides synthesis, which is costly and time consuming, but is necessary for the accurate measurement of binding kinetics in order to properly triage the best peptide leads during the affinity maturation stages. A sensitive technology is needed for directly measuring the binding kinetics of peptides on phages to reduce the time and cost of the entire process. Here, we show the capability of a charge-sensitive optical detection (CSOD) method for the direct quantification of binding kinetics of phage-displayed peptides to their target protein, using whole phages. We anticipate CSOD will contribute to streamline the process of phage display-based drug discovery.

Indexed as

BacteriophagesPeptide LibraryKineticsLigandsPeptidesProtein BindingLigandsPeptide LibraryPeptidesbinding kineticscharge-sensitive optical detectionlabel-freepeptidephage-displayprotein

Identifiers

PMID35735542
PMCPMC9221260

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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.