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Article << Previous     |     Next >>   Contents Vol 62(10)

Rapid Access to ω-Conotoxin Chimeras using Native Chemical Ligation

Gene Hopping A, Richard J. Lewis A, Paul F. Alewood A B

A Institute for Molecular Bioscience, The University of Queensland, St Lucia, Qld 4072, Australia.
B Corresponding author. Email: P.Alewood@imb.uq.edu.au
 
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Abstract

Grafting different regions of related peptides together to form a single protein chimera is a valuable tool in rapidly elucidating regions of activity or selectivity in peptides and proteins. To conveniently evaluate the contributions of the N- and C-terminal segments of ω-conotoxins CVID and MVIIC to activity, we employed native chemical ligation in CVID-MVIIC chimera design. Assembly of these peptide segments via the ligation method improved overall yield and coupling efficiency, with no difficult sequences encountered in contrast to the traditional full-length chain assembly of CVID. Radio-ligand binding assays revealed regions of importance for receptor recognition.

   
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