Hemolytic Activity of Antimicrobial Peptides

For antimicrobial peptides to be interesting for systemic applications, they must show low toxicity against erythrocytes. In this chapter, we describe a protocol for measuring the ability of AMPs to lyse human red blood cells, using melittin as positive control.

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Published inMethods in molecular biology (Clifton, N.J.) Vol. 1548; p. 427
Main Authors Oddo, Alberto, Hansen, Paul R
Format Journal Article
LanguageEnglish
Published United States 2017
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Abstract For antimicrobial peptides to be interesting for systemic applications, they must show low toxicity against erythrocytes. In this chapter, we describe a protocol for measuring the ability of AMPs to lyse human red blood cells, using melittin as positive control.
AbstractList For antimicrobial peptides to be interesting for systemic applications, they must show low toxicity against erythrocytes. In this chapter, we describe a protocol for measuring the ability of AMPs to lyse human red blood cells, using melittin as positive control.
Author Hansen, Paul R
Oddo, Alberto
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  organization: Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark
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  givenname: Paul R
  surname: Hansen
  fullname: Hansen, Paul R
  email: prh@sund.ku.dk
  organization: Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark. prh@sund.ku.dk
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Keywords Hemolysis
Melittin
Red blood cells
Antimicrobial peptides
Language English
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Snippet For antimicrobial peptides to be interesting for systemic applications, they must show low toxicity against erythrocytes. In this chapter, we describe a...
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StartPage 427
SubjectTerms Anti-Infective Agents - pharmacology
Antimicrobial Cationic Peptides - pharmacology
Dose-Response Relationship, Drug
Erythrocytes - drug effects
Hemolysis - drug effects
Humans
Melitten - pharmacology
Title Hemolytic Activity of Antimicrobial Peptides
URI https://www.ncbi.nlm.nih.gov/pubmed/28013523
Volume 1548
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