Specific and covalent labeling of a membrane protein with organic fluorochromes and quantum dots
Author(s) -
Roberto Bonasio,
Christopher V. Carman,
Enoch Kim,
Peter T. Sage,
Kerry R. Love,
Thorsten R. Mempel,
Timothy A. Springer,
Ulrich H. von Andrian
Publication year - 2007
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0705201104
Subject(s) - covalent bond , cutinase , biophysics , phosphonate , biochemistry , chemistry , quantum dot , biology , microbiology and biotechnology , enzyme , nanotechnology , materials science , organic chemistry
The real-time observation of protein dynamics in living cells and organisms is of fundamental importance for understanding biological processes. Most approaches to labeling proteins exploit noncovalent interactions, unsuitable to long-term studies, or genetic fusion to naturally occurring fluorescent proteins that often have unsatisfactory optical properties. Here we used the fungal enzyme cutinase and its suicide substrate p-nitrophenyl phosphonate to covalently attach a variety of labels to the integrin lymphocyte function-associated antigen-1 (LFA-1) on the surface of living cells. Cutinase was embedded in the extracellular domain of LFA-1 with no appreciable influence on integrin function and conformational regulation. p-nitrophenyl phosphonate-conjugated fluorochromes, including the very bright and stable quantum dots, bound efficiently and specifically to LFA-1/cutinase. The availability of a genetically encoded tag that binds covalently to quantum dots could foster the development of new experimental strategies for the study of protein dynamics in vivo.
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