Substituting azobenzene for proline in melittin to create photomelittin: A light-controlled membrane active peptide.

Biochim Biophys Acta Biomembr

Department of Chemistry and Biochemistry, Seton Hall University, South Orange, NJ, United States of America. Electronic address:

Published: December 2021

In this article we present the synthesis and characterization of a new form of the membrane active peptide melittin: photomelittin. This peptide was created by substituting the proline residue in melittin for a synthetic azobenzene amino acid derivative. This azobenzene altered the membrane activity of the peptide while retaining much of the secondary structure. Furthermore, the peptide demonstrates added light-dependent activity in leakage assays. There is a 1.5-fold increase in activity when exposed to UV light as opposed to visible light. The peptides further exhibit light-dependent hemolytic activity against human red blood cells. This will enable future studies optimizing photomelittin and other azobenzene-containing membrane active peptides for uses in medicine, drug delivery, and other biotechnological applications.

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http://dx.doi.org/10.1016/j.bbamem.2021.183759DOI Listing

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