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High content analysis to determine cytotoxicity of the antimicrobial peptide, melittin and selected structural analogs

High content analysis for cytoxicity of peptides on epithelial cells. Images of dye-loaded cells are acquired via multi-well automation by epifluorescence microscopy and are then subjected to segmentation analysis. [Display omitted] ► We describe a multi-parameter high-content analysis protocol for...

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Published in:Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2011-08, Vol.32 (8), p.1764-1773
Main Authors: Walsh, Edwin G., Maher, Sam, Devocelle, Marc, O’Brien, Peter J., Baird, Alan W., Brayden, David J.
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cited_by cdi_FETCH-LOGICAL-c501t-ac812dcf09c72a6035337a2b9c1146be52c563b8a6774319c04cbc52dd01ea773
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container_issue 8
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container_title Peptides (New York, N.Y. : 1980)
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creator Walsh, Edwin G.
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description High content analysis for cytoxicity of peptides on epithelial cells. Images of dye-loaded cells are acquired via multi-well automation by epifluorescence microscopy and are then subjected to segmentation analysis. [Display omitted] ► We describe a multi-parameter high-content analysis protocol for assessing peptide toxicity on epithelial cells. ► Selected deletion of amino acids of the bee venom, melittin, reduces its cytotoxicity. ► Loss of cytotoxicity was correlated with loss of epithelial permeation enhancement but not a reduction in antimicrobial activity. Antimicrobial peptides (AMPs) are naturally occurring entities with potential as pharmaceutical candidates and/or food additives. They are present in many organisms including bacteria, insects, fish and mammals. While their antimicrobial activity is equipotent with many commercial antibiotics, current limitations are poor pharmacokinetics, stability and potential toxicology issues. Most elicit antimicrobial action via perturbation of bacterial membranes. Consequently, associated cytotoxicity in human cells is reflected by their capacity to lyse erythrocytes. However, more rigorous toxicological assessment of AMPs is required in order to predict potential failure at a later stage of development. We describe a high-content analysis (HCA) screening protocol recently established for determination and prediction of safety in pharmaceutical drug discovery. HCA is a powerful, multi-parameter bioanalytical tool that amalgamates the actions of fluorescence microscopy with automated cell analysis software in order to understand multiple changes in cellular health. We describe the application of HCA in assessing cytotoxicity of the cytolytic α-helical peptide, melittin, and selected structural analogs. The data shows that structural modification of melittin reduces its cytotoxic action and that HCA is suitable for rapidly identifying cytotoxicity.
doi_str_mv 10.1016/j.peptides.2011.06.006
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identifier ISSN: 0196-9781
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1873-5169
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source ScienceDirect Freedom Collection
subjects anti-infective properties
antibiotics
Antimicrobial Cationic Peptides - chemistry
Antimicrobial Cationic Peptides - pharmacology
Antimicrobial peptide
antimicrobial peptides
antimicrobials
bacteria
Biological and medical sciences
Caco-2 Cells
computer software
cytotoxicity
Cytotoxicity screening
developmental stages
drugs
erythrocytes
fish
fluorescence microscopy
food additives
Fundamental and applied biological sciences. Psychology
High-content-analysis (HCA)
Humans
insects
Melitten - chemistry
Melitten - pharmacology
Melittin
MTT assay
pharmacokinetics
prediction
screening
toxicity testing
Vertebrates: endocrinology
title High content analysis to determine cytotoxicity of the antimicrobial peptide, melittin and selected structural analogs
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