Literature DB >> 26648572

The proteome targets of intracellular targeting antimicrobial peptides.

Pramod Shah1,2, Felix Shih-Hsiang Hsiao1,2, Yu-Hsuan Ho1,2, Chien-Sheng Chen1,2.   

Abstract

Antimicrobial peptides have been considered well-deserving candidates to fight the battle against microorganisms due to their broad-spectrum antimicrobial activities. Several studies have suggested that membrane disruption is the basic mechanism of AMPs that leads to killing or inhibiting microorganisms. Also, AMPs have been reported to interact with macromolecules inside the microbial cells such as nucleic acids (DNA/RNA), protein synthesis, essential enzymes, membrane septum formation and cell wall synthesis. Proteins are associated with many intracellular mechanisms of cells, thus protein targets may be specifically involved in mechanisms of action of AMPs. AMPs like pyrrhocoricin, drosocin, apidecin and Bac 7 are documented to have protein targets, DnaK and GroEL. Moreover, the intracellular targeting AMPs are reported to influence more than one protein targets inside the cell, suggesting for the multiple modes of actions. This complex mechanism of intracellular targeting AMPs makes them more difficult for the development of resistance. Herein, we have summarized the current status of AMPs in terms of their mode of actions, entry to cytoplasm and inhibition of macromolecules. To reveal the mechanism of action, we have focused on AMPs with intracellular protein targets. We have also included the use of high-throughput proteome microarray to determine the unidentified AMP protein targets in this review.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Antimicrobial peptides; Intracellular targets; Mechanism of action; Protein arrays; Protein targets; Proteome microarray

Mesh:

Substances:

Year:  2016        PMID: 26648572     DOI: 10.1002/pmic.201500380

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  22 in total

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Review 5.  Bioactive Peptides.

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6.  Systemic Responses of Multidrug-Resistant Pseudomonas aeruginosa and Acinetobacter baumannii Following Exposure to the Antimicrobial Peptide Cathelicidin-BF Imply Multiple Intracellular Targets.

Authors:  Cunbao Liu; Bin Shan; Jialong Qi; Yanbing Ma
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Journal:  Biomolecules       Date:  2020-04-23

8.  Mechanisms driving the antibacterial and antibiofilm properties of Hp1404 and its analogue peptides against multidrug-resistant Pseudomonas aeruginosa.

Authors:  Min Kyung Kim; Hee Kyoung Kang; Su Jin Ko; Min Ji Hong; Jeong Kyu Bang; Chang Ho Seo; Yoonkyung Park
Journal:  Sci Rep       Date:  2018-01-29       Impact factor: 4.379

9.  Transcriptional Responses of Candida albicans to Antimicrobial Peptide MAF-1A.

Authors:  Tao Wang; Jiangfan Xiu; Yingchun Zhang; Jianwei Wu; Xiaolin Ma; Yu Wang; Guo Guo; Xiaoli Shang
Journal:  Front Microbiol       Date:  2017-05-17       Impact factor: 5.640

10.  Tachyplesin Causes Membrane Instability That Kills Multidrug-Resistant Bacteria by Inhibiting the 3-Ketoacyl Carrier Protein Reductase FabG.

Authors:  Cunbao Liu; Jialong Qi; Bin Shan; Yanbing Ma
Journal:  Front Microbiol       Date:  2018-05-01       Impact factor: 5.640

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