Methods for imaging and analyses of intracellular organelles using fluorescent and luminescent proteins.

One of the important features of eukaryotic cells is the presence of intracellular compartments, organelles. Each organelle plays an essential role in the organelle-specific function; each cooperates with others for maintaining the vital activity of living cells. To analyze the organelle-specific functions, researchers have used many fluorescent and luminescent reporter proteins extensively. The reporter proteins have provided unprecedented insights into the movement of proteins and their interactions in the organelles. In this review, we summarize recently validated methods for visualizing protein localization, dynamics and protein-protein interactions, and for identifying a series of proteins localized in organelles using newly developed reporter proteins.

[1]  Shin-ichi Arimura,et al.  Frequent fusion and fission of plant mitochondria with unequal nucleoid distribution. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[2]  R. Rosenfeld Nature , 2009, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

[3]  J. Lippincott-Schwartz,et al.  Fluorescence protease protection of GFP chimeras to reveal protein topology and subcellular localization , 2006, Nature Methods.

[4]  M. J. Cormier,et al.  Primary structure of the Aequorea victoria green-fluorescent protein. , 1992, Gene.

[5]  Atsushi Miyawaki,et al.  A fluorescent variant of a protein from the stony coral Montipora facilitates dual-color single-laser fluorescence cross-correlation spectroscopy , 2006, Nature Biotechnology.

[6]  A. Miyawaki,et al.  An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[7]  Peter K. Kim,et al.  JCB: ARTICLE The , 2022 .

[8]  Yoshio Umezawa,et al.  A genetic approach to identifying mitochondrial proteins , 2003, Nature Biotechnology.

[9]  A. Miyawaki,et al.  Regulated Fast Nucleocytoplasmic Shuttling Observed by Reversible Protein Highlighting , 2004, Science.

[10]  Y. Umezawa,et al.  Quantitative determination of protein nuclear transport induced by phosphorylation or by proteolysis. , 2005, Analytical chemistry.

[11]  Konstantin A Lukyanov,et al.  Photoswitchable cyan fluorescent protein for protein tracking , 2004, Nature Biotechnology.

[12]  S. Michnick,et al.  Capturing protein interactions in the secretory pathway of living cells. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[13]  G. G. Stokes "J." , 1890, The New Yale Book of Quotations.

[14]  Y. Umezawa,et al.  High-throughput sensing and noninvasive imaging of protein nuclear transport by using reconstitution of split Renilla luciferase. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[15]  George H. Patterson,et al.  A Photoactivatable GFP for Selective Photolabeling of Proteins and Cells , 2002, Science.

[16]  R. Tsien,et al.  A monomeric red fluorescent protein , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[17]  宁北芳,et al.  疟原虫var基因转换速率变化导致抗原变异[英]/Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A , 2005 .