Issue 3, 2016

Total chemical synthesis of photoactivatable proteins for light-controlled manipulation of antigen–antibody interactions

Abstract

We report the chemical synthesis of the first photo-activatable protein antigen that can be used to study antigen–antibody interaction mediated responses in B cells. This strategy facilitated fine tuning of the caged protein antigen to optimize its bioactivity and photochemical properties. One optimal molecule, HEL-K96NPE, was totally inert to hen egg lysozyme (HEL)-specific B cells and could only restore its antigenicity upon photoactivation. Combined with real time live cell imaging, the utility of HEL-K96NPE was demonstrated as a proof of concept to quantify B cell synapse formation and calcium influx responses at the single cell level.

Graphical abstract: Total chemical synthesis of photoactivatable proteins for light-controlled manipulation of antigen–antibody interactions

Supplementary files

Article information

Article type
Edge Article
Submitted
10 Sep 2015
Accepted
19 Nov 2015
First published
11 Dec 2015
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2016,7, 1891-1895

Total chemical synthesis of photoactivatable proteins for light-controlled manipulation of antigen–antibody interactions

S. Tang, Z. Wan, Y. Gao, J. Zheng, J. Wang, Y. Si, X. Chen, H. Qi, L. Liu and W. Liu, Chem. Sci., 2016, 7, 1891 DOI: 10.1039/C5SC03404C

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.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements