Issue 50, 2015

Reversible thermo-sensitivity induced from varying the hydrogen bonding between the side residues of rationally designed polypeptides

Abstract

Rationally designed polypeptides with similar molecular structures but varying patterns of hydrogen bonding between the side groups have been synthesized and demonstrated to possess distinct solubility and thermal behaviors. Further balancing the ratio of both isopropylamine and ethylenediamine side groups endows the random copolymer with reversible thermo-sensitivity.

Graphical abstract: Reversible thermo-sensitivity induced from varying the hydrogen bonding between the side residues of rationally designed polypeptides

Supplementary files

Article information

Article type
Communication
Submitted
11 Apr 2015
Accepted
13 May 2015
First published
13 May 2015

Chem. Commun., 2015,51, 10174-10177

Author version available

Reversible thermo-sensitivity induced from varying the hydrogen bonding between the side residues of rationally designed polypeptides

H. Liu, Y. Xiao, H. Xu, Y. Guan, J. Zhang and M. Lang, Chem. Commun., 2015, 51, 10174 DOI: 10.1039/C5CC03017J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements