Issue 46, 2022

Membrane targeting enhances muramyl dipeptide binding to NOD2 and Arf6–GTPase in mammalian cells

Abstract

To further understand the mechanisms of muramyl dipeptide (MDP) sensing by NOD2, we evaluated key properties involved in the formation of the Arf6–MDP–NOD2 complex in mammalian cells. We found that the conserved Arf aromatic triad is crucial for binding to MDP–NOD2. Mutation of Arf6 N-myristoylation and NOD2 S-palmitoylation also abrogated the formation of the Arf6–MDP–NOD2 complex. Notably, lipid-modified MDP (L18-MDP) increased Arf6–NOD2 assembly. Our results indicate recruitment of Arf6 may explain enhanced activity of lipidated MDP analogues and membrane targeting may be important in developing next-generation NOD2 agonists.

Graphical abstract: Membrane targeting enhances muramyl dipeptide binding to NOD2 and Arf6–GTPase in mammalian cells

Supplementary files

Article information

Article type
Communication
Submitted
07 4月 2022
Accepted
10 5月 2022
First published
18 5月 2022

Chem. Commun., 2022,58, 6598-6601

Membrane targeting enhances muramyl dipeptide binding to NOD2 and Arf6–GTPase in mammalian cells

C. W. Hespen, X. Zhao and H. C. Hang, Chem. Commun., 2022, 58, 6598 DOI: 10.1039/D2CC01903E

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