| Literature DB >> 35013238 |
Cheng-Yu Tsai1,2,3, Emmanuel Oluwatobi Salawu1,4,5, Hongchun Li1,6,7,8, Guan-Yu Lin9, Ting-Yu Kuo9, Liyin Voon1, Adarsh Sharma1, Kai-Di Hu1, Yi-Yun Cheng10, Sobha Sahoo1, Lutimba Stuart1, Chih-Wei Chen1, Yuan-Yu Chang1,10, Yu-Lin Lu1, Simai Ke1, Christopher Llynard D Ortiz1,11,12, Bai-Shan Fang7,13, Chen-Chi Wu3,14, Chung-Yu Lan15,16, Hua-Wen Fu17,18, Lee-Wei Yang19,20,21,22.
Abstract
The systematic design of functional peptides has technological and therapeutic applications. However, there is a need for pattern-based search engines that help locate desired functional motifs in primary sequences regardless of their evolutionary conservation. Existing databases such as The Protein Secondary Structure database (PSS) no longer serves the community, while the Dictionary of Protein Secondary Structure (DSSP) annotates the secondary structures when tertiary structures of proteins are provided. Here, we extract 1.7 million helices from the PDB and compile them into a database (Therapeutic Peptide Design database; TP-DB) that allows queries of compounded patterns to facilitate the identification of sequence motifs of helical structures. We show how TP-DB helps us identify a known purification-tag-specific antibody that can be repurposed into a diagnostic kit for Helicobacter pylori. We also show how the database can be used to design a new antimicrobial peptide that shows better Candida albicans clearance and lower hemolysis than its template homologs. Finally, we demonstrate how TP-DB can suggest point mutations in helical peptide blockers to prevent a targeted tumorigenic protein-protein interaction. TP-DB is made available at http://dyn.life.nthu.edu.tw/design/ .Entities:
Mesh:
Substances:
Year: 2022 PMID: 35013238 PMCID: PMC8748493 DOI: 10.1038/s41467-021-27655-0
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 17.694