A photoactivatable Src homology 2 (SH2) domain. Issue 56 (25th May 2016)

• Record Type: Journal Article
• Authors: Song, X.; Shang, X.; Ju, T.; Cerny, R.; Niu, W.; Guo, J.
• Is Part Of: RSC advances. Volume 6:Issue 56(2016)
• Page Start: 51120
• Page End: 51124
• Publication Date: 2016-05-25
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra06211c
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : A photoactivatable SH2 domain that can be potentially applied as an optogenetic tool to the photocontrol of phosphotyrosine-associated biological processes. Abstract : Src homology 2 (SH2) domains bind specifically to phosphotyrosine-containing motifs. As a regulatory module of intracellular signaling cascades, the SH2 domain plays important roles in the signal transduction of receptor tyrosine kinase pathways. In this work, we reported the construction of a photoactivatable SH2 domain through the combination of protein engineering and genetic incorporation of photo-caged unnatural amino acids. Significantly enhanced recognition of a phosphotyrosine-containing peptide substrate by the engineered SH2 domain mutant was observed after light-induced removal of the photo-caging group. Optical activation allows the control of protein and/or cellular function with temporal and spatial resolution. This photoactivatable SH2 domain could potentially be applied to the study of tyrosine phsophorylation-associated biological processes.