Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published December 23, 2013 | Supplemental Material + Accepted Version
Journal Article Open

A Chemical Epitope-Targeting Strategy for Protein Capture Agents: The Serine 474 Epitope of the Kinase Akt2

Abstract

Target and click: Peptide ligands targeted to the C-terminal motif of the kinase Akt2 were obtained by combining phosphate recognition of a dinuclear zinc(II) complex with in situ click chemistry to target this epitope. The peptide ligands (shown as XXXXX) selectively bind the C-terminal polypeptide of Akt2, and are selective for Akt2 relative to the Akt1 and Akt3 isoforms. The ligands differentially modulate Akt2 activity.

Additional Information

© 2013 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. Received: July 7, 2013; Revised: September 23, 2013. Article first published online: 19 Nov. 2013. This work was supported by the Institute for Collaborative Biotechnologies through grant W911NF-09-0001 from the U.S. Army Research Office. Additional personnel or facilities support from the National Cancer Institute (5U54 CA119347: J.R.H. PI), the Grand Duchy of Luxembourg, and the Bill and Melinda Gates Foundation is acknowledged.

Attached Files

Accepted Version - nihms589080.pdf

Supplemental Material - anie_201305882_sm_miscellaneous_information.pdf

Files

anie_201305882_sm_miscellaneous_information.pdf
Files (21.4 MB)
Name Size Download all
md5:585779eb818c5d5bd750c77f8616985f
19.9 MB Preview Download
md5:bfc5a9b437d6416605e0e98d10bea05e
1.5 MB Preview Download

Additional details

Created:
August 22, 2023
Modified:
October 25, 2023