Green fluorescent protein labeling of cytoskeletal structures - Novel targeting approach based on leucine zippers

被引:22
作者
Katz, BZ
Krylov, D
Aota, SI
Olive, M
Vinson, C
Yamada, KM
机构
[1] NIDR, Craniofacial Dev Biol & Regenerat Branch, NIH, Bethesda, MD 20892 USA
[2] NCI, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.2144/98252rr01
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:298 / +
页数:5
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