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Molecular Engineering for Imaging and Reprogramming in Live Cells
Author(s) -
Wang Peter Yingxiao,
Sun Jie,
Lei Lei
Publication year - 2016
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.30.1_supplement.228.2
Subject(s) - förster resonance energy transfer , phosphorylation , microbiology and biotechnology , biophysics , cell signaling , chemistry , protein tyrosine phosphatase , tyrosine , reprogramming , live cell imaging , sh2 domain , intramolecular force , protein engineering , signal transduction , biochemistry , biology , cell , fluorescence , stereochemistry , enzyme , physics , quantum mechanics
Signaling molecules and their activities are well coordinated in space and time to regulate cellular functions in response to mechanical and chemical microenvironment. Based on fluorescent resonance energy transfer (FRET), we have developed genetically encoded biosensors to monitor the dynamic molecular activities (such as Src and FAK activities) in live cells at subcellular compartments when cells interact with their neighbors or mechanical/chemical microenvironment. In a recent study, we show that a ubiquitous signaling protein, Src Homology2 (SH2) Domain‐containing Protein Tyrosine Phosphatase 2 (Shp2), displayed unexpected plasticity of conformational changes via intramolecular interactions within Shp2 ( cis ‐interaction). We found that two phosphorylated regulatory tyrosines upon stimulated phosphorylation can compete for the cis ‐interaction of the same SH2 domain within Shp2 to achieve plasticity. The antagonistic combination of contextual amino acid sequence and position can create arelatively small difference between the two phosphorylated tyrosines in their overall competitiveness for intramolecular conformational regulation. Enlarging this difference by swapping the sequences at the two tyrosine positions resulted in loss of conformational plasticity and reprogrammed downstream ERK signaling dynamics. We have further engineered a machinery molecule based onShp2 which allows an integrated capability of imaging and manipulation of single cell life. We suggest that this strategy can serve as a general and basic design principle for natural and synthetic proteins, with their conformations and functions tunable to regulate downstream physiological consequences. As such, molecular engineering and biosensor development can provide powerful tools for the imaging and manipulation of cellular lives at single cell levels. Support or Funding Information This work is supported in part by NIHHL098472, HL109142, HL121365, NSF CBET1360341, UC San Diego.