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.

Differences in the conformational energy landscape of CDK1 and CDK2 suggest a mechanism for achieving selective CDK inhibition

Lookup NU author(s): Daniel Wood, Svitlana Korolchuk, Dr Natalie TatumORCiD, Lan Wang, Professor Jane EndicottORCiD, Professor Martin NobleORCiD, Dr Mathew MartinORCiD

Downloads


Licence

This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

Dysregulation of the cell cycle characterises many cancer subtypes, providing a rationale for developing cyclin-dependent kinase (CDK) inhibitors. Potent CDK2 inhibitors might target certain cancers in which CCNE1 is amplified. However, current CDK2 inhibitors also inhibit CDK1, generating a toxicity liability. We have used biophysical measurements and X-ray crystallography to investigate the ATP-competitive inhibitor binding properties of cyclin-free and cyclin-bound CDK1 and CDK2. We show that these kinases can readily be distinguished by such inhibitors when cyclin-free, but not when cyclin-bound. The basis for this discrimination is unclear from either inspection or molecular dynamics simulation of ligand-bound CDKs, but is reflected in the contacts made between the kinase N- and C-lobes. We conclude that there is a subtle but profound difference between the conformational energy landscapes of cyclin-free CDK1 and CDK2. The unusual properties of CDK1 might be exploited to differentiate CDK1 from other CDKs in future cancer therapeutic design.


Publication metadata

Author(s): Wood DJ, Korolchuk S, Tatum NJ, Wang L-Z, Endicott JA, Noble MEM, Martin MP

Publication type: Article

Publication status: Published

Journal: Cell Chemical Biology

Year: 2019

Volume: 26

Issue: 1

Pages: 121-130.e5

Print publication date: 17/01/2019

Online publication date: 21/11/2018

Acceptance date: 11/10/2018

Date deposited: 25/10/2018

ISSN (print): 2451-9456

ISSN (electronic): 2451-9448

Publisher: Cell Press

URL: https://doi.org/10.1016/j.chembiol.2018.10.015

DOI: 10.1016/j.chembiol.2018.10.015


Altmetrics

Altmetrics provided by Altmetric


Funding

Funder referenceFunder name
C2115/A21421Cancer Research UK CRUK (closed comp)
MR/N009738/1Medical Research Council (MRC)

Share