Handedness preference and switching of peptide helices. Part II: Helices based on noncoded α-amino acids.

Marco Crisma, Marta De Zotti, Fernando Formaggio, Cristina Peggion, Alessandro Moretto, Claudio Toniolo

Journal: Journal of peptide science : an official publication of the European Peptide Society 2015;21(3):148-77

PMID: 25640955

Abstract

In this second part of our review article on the preferred screw sense and interconversion of peptide helices, we discuss the most significant computational and experimental data published on helices formed by the most extensively investigated categories of noncoded α-amino acids. They are as follows: (i) N-alkylated Gly residues (peptoids), (ii) C(α) -alkylated α-amino acids, (iii) C(α,β) -sp(2) configurated α-amino acids, and (iv) combinations of residues of types (ii) and (iii). With confidence, the large body of interesting papers examined and classified in this editorial effort will stimulate the development of helical peptides in many diverse areas of biosciences and nanosciences.

Copyright © 2015 European Peptide Society and John Wiley & Sons, Ltd.

Address: ICB, Padova Unit, CNR, Padova, Italy.
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.