Literature DB >> 35013238

Helical structure motifs made searchable for functional peptide design.

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/ .
© 2022. The Author(s).

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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


  44 in total

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Journal:  Probiotics Antimicrob Proteins       Date:  2012-06       Impact factor: 4.609

Review 2.  Glycogen phosphorylase. The structural basis of the allosteric response and comparison with other allosteric proteins.

Authors:  L N Johnson; D Barford
Journal:  J Biol Chem       Date:  1990-02-15       Impact factor: 5.157

3.  Resolution-exchanged structural modeling and simulations jointly unravel that subunit rolling underlies the mechanism of programmed ribosomal frameshifting.

Authors:  Kai-Chun Chang; Emmanuel Oluwatobi Salawu; Yuan-Yu Chang; Jin-Der Wen; Lee-Wei Yang
Journal:  Bioinformatics       Date:  2019-03-15       Impact factor: 6.937

4.  Ligand-induced protein responses and mechanical signal propagation described by linear response theories.

Authors:  Lee-Wei Yang; Akio Kitao; Bang-Chieh Huang; Nobuhiro Gō
Journal:  Biophys J       Date:  2014-09-16       Impact factor: 4.033

5.  Two nuclear localization signals present in the basic-helix 1 domains of MyoD promote its active nuclear translocation and can function independently.

Authors:  M Vandromme; J C Cavadore; A Bonnieu; A Froeschlé; N Lamb; A Fernandez
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

6.  Structure and function of the PP2A-shugoshin interaction.

Authors:  Zheng Xu; Bulent Cetin; Martin Anger; Uhn Soo Cho; Wolfgang Helmhart; Kim Nasmyth; Wenqing Xu
Journal:  Mol Cell       Date:  2009-08-28       Impact factor: 17.970

7.  In silico optimization of a guava antimicrobial peptide enables combinatorial exploration for peptide design.

Authors:  William F Porto; Luz Irazazabal; Eliane S F Alves; Suzana M Ribeiro; Carolina O Matos; Állan S Pires; Isabel C M Fensterseifer; Vivian J Miranda; Evan F Haney; Vincent Humblot; Marcelo D T Torres; Robert E W Hancock; Luciano M Liao; Ali Ladram; Timothy K Lu; Cesar de la Fuente-Nunez; Octavio L Franco
Journal:  Nat Commun       Date:  2018-04-16       Impact factor: 14.919

8.  Molecular dynamics simulations and linear response theories jointly describe biphasic responses of myoglobin relaxation and reveal evolutionarily conserved frequent communicators.

Authors:  Bang-Chieh Huang; Lee-Wei Yang
Journal:  Biophys Physicobiol       Date:  2019-11-29

9.  Helical antimicrobial peptides assemble into protofibril scaffolds that present ordered dsDNA to TLR9.

Authors:  Ernest Y Lee; Changsheng Zhang; Jeremy Di Domizio; Fan Jin; Will Connell; Mandy Hung; Nicolas Malkoff; Veronica Veksler; Michel Gilliet; Pengyu Ren; Gerard C L Wong
Journal:  Nat Commun       Date:  2019-03-04       Impact factor: 14.919

10.  Mapping the orientation of helices in micelle-bound peptides by paramagnetic relaxation waves.

Authors:  Michal Respondek; Tobias Madl; Christoph Göbl; Regina Golser; Klaus Zangger
Journal:  J Am Chem Soc       Date:  2007-03-31       Impact factor: 15.419

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