Literature DB >> 17266652

Tool developments for structure-function studies of host defense peptides.

Guangshun Wang1.   

Abstract

Antimicrobial peptides, or host defense peptides, are universal signaling and effector molecules in host defense and innate immunity. This article highlights various tools developed for cathelicidins and defensins, ranging from peptide identification, production, and structural biology, including the eight databases for antimicrobial peptides. Novel peptides can be identified from natural sources at both gene and protein levels. Solid-phase synthesis and bacterial expression are the two important methods for peptide production. Three-dimensional structures of antimicrobial peptides, primarily determined by solution NMR techniques, are essential for an in-depth understanding of the mode of action. The introduction of octanoyl phosphatidylglycerol as a bacterial membrane-mimetic model provides new insights into peptide-lipid interactions. The incorporation of structure and activity data into the antimicrobial peptide database (http://aps.unmc.edu/AP/main.html) will lead to an integrated understanding of these peptides via structural bioinformatics.

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Year:  2007        PMID: 17266652     DOI: 10.2174/092986607779117182

Source DB:  PubMed          Journal:  Protein Pept Lett        ISSN: 0929-8665            Impact factor:   1.890


  8 in total

1.  Natural History of Innate Host Defense Peptides.

Authors:  A Linde; B Wachter; O P Höner; L Dib; C Ross; A R Tamayo; F Blecha; T Melgarejo
Journal:  Probiotics Antimicrob Proteins       Date:  2009-12       Impact factor: 4.609

2.  Anti-human immunodeficiency virus type 1 activities of antimicrobial peptides derived from human and bovine cathelicidins.

Authors:  Guangshun Wang; Karen M Watson; Robert W Buckheit
Journal:  Antimicrob Agents Chemother       Date:  2008-06-30       Impact factor: 5.191

Review 3.  High-quality 3D structures shine light on antibacterial, anti-biofilm and antiviral activities of human cathelicidin LL-37 and its fragments.

Authors:  Guangshun Wang; Biswajit Mishra; Raquel F Epand; Richard M Epand
Journal:  Biochim Biophys Acta       Date:  2014-01-23

4.  Lipid segregation explains selective toxicity of a series of fragments derived from the human cathelicidin LL-37.

Authors:  Raquel F Epand; Guangshun Wang; Bob Berno; Richard M Epand
Journal:  Antimicrob Agents Chemother       Date:  2009-07-06       Impact factor: 5.191

5.  Self-assembly of glycerol monooleate with the antimicrobial peptide LL-37: a molecular dynamics study.

Authors:  R Innocenti Malini; M Zabara; M Gontsarik; K Maniura-Weber; R M Rossi; F Spano; S Salentinig
Journal:  RSC Adv       Date:  2020-02-26       Impact factor: 4.036

6.  APD2: the updated antimicrobial peptide database and its application in peptide design.

Authors:  Guangshun Wang; Xia Li; Zhe Wang
Journal:  Nucleic Acids Res       Date:  2008-10-28       Impact factor: 16.971

7.  Piloting the membranolytic activities of peptides with a self-organizing map.

Authors:  Yen-Chu Lin; Jan A Hiss; Petra Schneider; Peter Thelesklaf; Yi Fan Lim; Max Pillong; Fabian M Koehler; Petra S Dittrich; Cornelia Halin; Silja Wessler; Gisbert Schneider
Journal:  Chembiochem       Date:  2014-09-09       Impact factor: 3.164

8.  APD3: the antimicrobial peptide database as a tool for research and education.

Authors:  Guangshun Wang; Xia Li; Zhe Wang
Journal:  Nucleic Acids Res       Date:  2015-11-23       Impact factor: 16.971

  8 in total

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