Please use this identifier to cite or link to this item:
Title: Model membrane interaction and DNA-binding of antimicrobial peptide Lasioglossin II derived from bee venom
Authors: Bandyopadhyay, S.
Lee, M.
Sivaraman, J. 
Chatterjee, C.
Keywords: Antimicrobial peptide
Lasioglossin II
Issue Date: 4-Jan-2013
Citation: Bandyopadhyay, S., Lee, M., Sivaraman, J., Chatterjee, C. (2013-01-04). Model membrane interaction and DNA-binding of antimicrobial peptide Lasioglossin II derived from bee venom. Biochemical and Biophysical Research Communications 430 (1) : 1-6. ScholarBank@NUS Repository.
Abstract: Lasioglossins, a new family of antimicrobial peptide, have been shown to have strong antimicrobial activity with low haemo-lytic and mast cell degranulation activity, and exhibit cytotoxic activity against various cancer cells in vitro. In order to understand the active conformation of these pentadecapeptides in membranes, we have studied the interaction of Lasioglossin II (LL-II), one of the members of Lasioglossins family with membrane mimetic micelle Dodecylphosphocholine (DPC) by fluorescence, Circular Dichroism (CD) and two dimensional (2D) 1H NMR spectroscopy. Fluorescence experiments provide evidence of interaction of the N-terminal tryptophan residue of LL-II with the hydrophobic core of DPC micelle. CD results show an extended chain conformation of LL-II in water which is converted to a partial helical conformation in the presence of DPC micelle. Moreover we have determined the first three-dimensional NMR structure of LL-II bound to DPC micelle with rmsd of 0.36å. The solution structure of LL-II shows hydrophobic and hydrophilic core formation in peptide pointing towards different direction in the presence of DPC. This amphipathic structure may allow this peptide to penetrate deeply into the interfacial region of negatively charged membranes and leading to local membrane destabilization. Further we have elucidated the DNA binding ability of LL-II by agarose gel retardation and fluorescence quenching experiments. © 2012 Elsevier Inc.
Source Title: Biochemical and Biophysical Research Communications
ISSN: 0006291X
DOI: 10.1016/j.bbrc.2012.11.015
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.