Toggle Main Menu Toggle Search

Open Access padlockePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Selective recognition of the di/trimethylammonium motif by an artificial carboxycalixarene receptor

Lookup NU author(s): Professor Akane KawamuraORCiD

Downloads


Licence

This is the authors' accepted manuscript of an article that has been published in its final definitive form by Royal Society of Chemistry, 2017.

For re-use rights please refer to the publisher's terms and conditions.


Abstract

© The Royal Society of Chemistry. Chemical tools that recognise post-translational modifications have promising applications in biochemistry and in therapy. We report a simple carboxycalixarene that selectively binds molecules containing di/trimethylammonium moieties in isolation, in cell lysates and when incorporated in histone peptides. Our findings reveal the potential of using carboxycalixarene-based receptors to study epigenetic regulation.


Publication metadata

Author(s): Hanauer T, Hopkinson RJ, Patel K, Li Y, Correddu D, Kawamura A, Sarojini V, Leung IKH, Gruber T

Publication type: Article

Publication status: Published

Journal: Organic and Biomolecular Chemistry

Year: 2017

Volume: 15

Issue: 5

Pages: 1100-1105

Print publication date: 07/02/2017

Online publication date: 04/01/2017

Acceptance date: 03/01/2017

Date deposited: 14/10/2019

ISSN (print): 1477-0520

ISSN (electronic): 1477-0539

Publisher: Royal Society of Chemistry

URL: https://doi.org/10.1039/c6ob02616h

DOI: 10.1039/c6ob02616h


Altmetrics

Altmetrics provided by Altmetric


Share