Literature DB >> 9695812

GFP illuminates the cytoskeleton.

B Ludin1, A Matus.   

Abstract

Until recently, cytoskeleton research has relied primarily on immunofluorescence microscopy techniques, requiring fixation and hence killing of the specimen before the analysis. The sole method for visualizing cytoskeletal dynamics in living cells has been the microinjection of purified and fluorescently labelled protein, but technical difficulties have precluded its widespread use. The recent introduction of green fluorescent protein (GFP) has enabled visualization of proteins and cytoskeletal dynamics with only minimal perturbations of the living cell and has opened new horizons for studying the cytoskeleton.

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Year:  1998        PMID: 9695812

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  20 in total

1.  Cell cycle-dependent changes in microtubule dynamics in living cells expressing green fluorescent protein-alpha tubulin.

Authors:  N M Rusan; C J Fagerstrom; A M Yvon; P Wadsworth
Journal:  Mol Biol Cell       Date:  2001-04       Impact factor: 4.138

2.  Live-cell analysis of a green fluorescent protein-tagged herpes simplex virus infection.

Authors:  G Elliott; P O'Hare
Journal:  J Virol       Date:  1999-05       Impact factor: 5.103

Review 3.  Reporter gene vectors and assays.

Authors:  E Schenborn; D Groskreutz
Journal:  Mol Biotechnol       Date:  1999-11       Impact factor: 2.695

4.  Cytoskeletal microdifferentiation: a mechanism for organizing morphological plasticity in dendrites.

Authors:  S Kaech; H Parmar; M Roelandse; C Bornmann; A Matus
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-19       Impact factor: 11.205

5.  Axonal tau mRNA localization coincides with tau protein in living neuronal cells and depends on axonal targeting signal.

Authors:  S Aronov; G Aranda; L Behar; I Ginzburg
Journal:  J Neurosci       Date:  2001-09-01       Impact factor: 6.167

Review 6.  Studying cytoskeletal dynamics in living cells using green fluorescent protein.

Authors:  Yisang Yoon; Kelly Pitts; Mark McNiven
Journal:  Mol Biotechnol       Date:  2002-07       Impact factor: 2.695

7.  pSAT vectors: a modular series of plasmids for autofluorescent protein tagging and expression of multiple genes in plants.

Authors:  Tzvi Tzfira; Guo-Wei Tian; Benoît Lacroix; Shachi Vyas; Jianxiong Li; Yael Leitner-Dagan; Alexander Krichevsky; Tamir Taylor; Alexander Vainstein; Vitaly Citovsky
Journal:  Plant Mol Biol       Date:  2005-03       Impact factor: 4.076

8.  In vivo dynamics of the F-actin-binding protein neurabin-II.

Authors:  D J Stephens; G Banting
Journal:  Biochem J       Date:  2000-01-15       Impact factor: 3.857

9.  Zyxin is not colocalized with vasodilator-stimulated phosphoprotein (VASP) at lamellipodial tips and exhibits different dynamics to vinculin, paxillin, and VASP in focal adhesions.

Authors:  K Rottner; M Krause; M Gimona; J V Small; J Wehland
Journal:  Mol Biol Cell       Date:  2001-10       Impact factor: 4.138

10.  Modulating the function of the measles virus RNA-dependent RNA polymerase by insertion of green fluorescent protein into the open reading frame.

Authors:  W Paul Duprex; Fergal M Collins; Bert K Rima
Journal:  J Virol       Date:  2002-07       Impact factor: 5.103

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