Issue 11, 2015

Contributions of pocket depth and electrostatic interactions to affinity and selectivity of receptors for methylated lysine in water

Abstract

Dynamic combinatorial chemistry was used to generate a set of receptors for peptides containing methylated lysine (KMen, n = 0–3) and study the contribution of electrostatic effects and pocket depth to binding affinity and selectivity. We found that changing the location of a carboxylate resulted in an increase in preference for KMe2, presumably based on ability to form a salt bridge with KMe2. The number of charged groups on either the receptor or peptide guest systematically varied the binding affinities to all guests by approximately 1–1.5 kcal mol−1, with little influence on selectivity. Lastly, formation of a deeper pocket led to both increased affinity and selectivity for KMe3 over the lower methylation states. From these studies, we identified that the tightest binder was a receptor with greater net charge, with a Kd of 0.2 μM, and the receptor with the highest selectivity was the one with the deepest pocket, providing 14-fold selectivity between KMe3 and KMe2 and a Kd for KMe3 of 0.3 μM. This work provides key insights into approaches to improve binding affinity and selectivity in water, while also demonstrating the versatility of dynamic combinatorial chemistry for rapidly exploring the impact of subtle changes in receptor functionality on molecular recognition in water.

Graphical abstract: Contributions of pocket depth and electrostatic interactions to affinity and selectivity of receptors for methylated lysine in water

Supplementary files

Article information

Article type
Paper
Submitted
20 loka 2014
Accepted
20 marras 2014
First published
20 marras 2014

Org. Biomol. Chem., 2015,13, 3220-3226

Author version available

Contributions of pocket depth and electrostatic interactions to affinity and selectivity of receptors for methylated lysine in water

J. E. Beaver, B. C. Peacor, J. V. Bain, L. I. James and M. L. Waters, Org. Biomol. Chem., 2015, 13, 3220 DOI: 10.1039/C4OB02231A

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