Green Fluorescent Protein Labeling of Cytoskeletal Structures—Novel Targeting Approach Based on Leucine Zippers
Author(s) -
BenZion Katz,
D. Krylov,
S. Aota,
Michelle Olive,
Charles Vinson,
Kenneth M. Yamada
Publication year - 1998
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/98252rr01
Subject(s) - green fluorescent protein , fusion protein , leucine zipper , cytoskeleton , subcellular localization , protein subcellular localization prediction , microbiology and biotechnology , fluorescence , chemistry , biophysics , cytoplasm , biochemistry , biology , cell , peptide sequence , gene , physics , quantum mechanics , recombinant dna
Green fluorescent protein (GFP) is a valuable marker for intracellular protein localization. However the fusion of GFP with structural proteins can alter their properties, resulting in a loss of fusion protein localization, decreased GFP fluorescence or both. We describe a novel targeting approach based on noncovalent heterodimerization of GFP and cytoplasmic structural proteins. The formation of structural protein/GFP complexes was mediated by modified leucine zipper protein spacers designed to form high-affinity heterodimers. The complexes localized accurately to specific sites within cells, providing selective fluorescence labeling of subcellular structures such as microfilaments or focal contacts.
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