Issue 61, 2017

Synthesis of the Src SH2 domain and its application in bioassays for mirror-image screening

Abstract

The Src SH2 domain was synthesized via native chemical ligation of two fragment peptides. The facile protocol was used to prepare the mirror-image SH2 domain (D-Src SH2 domain) and tetramethylrhodamine-labeled SH2 domains. The synthesized SH2 domains were correctly folded and showed activity, and using these proteins we established bioassays to identify novel Src SH2 domain inhibitors from an unexplored mirror-image library of natural products.

Graphical abstract: Synthesis of the Src SH2 domain and its application in bioassays for mirror-image screening

Supplementary files

Article information

Article type
Paper
Submitted
06 Jul 2017
Accepted
28 Jul 2017
First published
07 Aug 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 38725-38732

Synthesis of the Src SH2 domain and its application in bioassays for mirror-image screening

K. Shu, T. Noguchi, K. Honda, Y. Kondoh, H. Osada, H. Ohno, N. Fujii and S. Oishi, RSC Adv., 2017, 7, 38725 DOI: 10.1039/C7RA07445J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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