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Screening of specific binding peptides using phage-display techniques and their biosensing applications

Authors
Xu, PingGhosh, SubhadeepGul, Anam RanaBhamore, Jigna R.Park, Jong PilPark, Tae Jung
Issue Date
Apr-2021
Publisher
Elsevier B.V.
Keywords
Biosensor; Colorimetric assay; Electrochemical sensor; Fluorescence biosensor; M13 phage; Peptide; Phage display; Surface plasmon resonance
Citation
TrAC - Trends in Analytical Chemistry, v.137
Journal Title
TrAC - Trends in Analytical Chemistry
Volume
137
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/43985
DOI
10.1016/j.trac.2021.116229
ISSN
0165-9936
1879-3142
Abstract
Biosensors have been explored for their excellent potential in the field of biological detection and their application in biomedical diagnosis and have become a rapidly emerging subject. The development of biosensors urgently needs support in the expansion of recognition elements. Sequential advancements in displayed peptide technology have been achieved by fusing phage display peptide libraries into phage coat proteins. Screening procedures for phage display readily recognize a variety of binding affinity peptides, which are alternatives to antibodies. The emergence of phage display peptides compensated for the lack of recognition molecules and has played an unprecedented role in the field of biosensing. Displayed peptides have been used for specific receptors in various biosensors in recent years because of advantages such as high affinity, low procedure cost, high purity and mass production, easy design and modification at the molecular level, and increased resistance to the sophisticated detection environment. This review summarizes the feasible applications of phage-displayed peptides in major biosensors and highlights both the outstanding performance and shortcomings of peptide sensors. © 2021 Elsevier B.V.
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