Enzyme-based protein-tagging systems for site-specific labeling of proteins in living cells

被引:3
作者
Sueda, Shinji [1 ,2 ]
机构
[1] Kyushu Inst Technol, Dept Biosci & Bioinformat, 680-4 Kawazu, Iizuka, Fukuoka 8208502, Japan
[2] Kyushu Inst Technol, Res Ctr Biomicrosensing Technol, Tobata Ku, 1-1 Sensui Cho, Kitakyushu, Fukuoka 8048550, Japan
关键词
protein labeling; protein-tagging system; fluorescent labeling; fluorescence imaging; enzyme reaction; post-translational modification; IN-VIVO; FLUORESCENT PROTEIN; MEMBRANE-PROTEIN; FUSION PROTEINS; SMALL MOLECULES; PEPTIDE-TAGS; LIGASE; SURFACE; LIGATION; SORTASE;
D O I
10.1093/jmicro/dfaa011
中图分类号
TH742 [显微镜];
学科分类号
摘要
Various protein-labeling methods based on the specific interactions between genetically encoded tags and synthetic probes have been proposed to complement fluorescent protein-based labeling. In particular, labeling methods based on enzyme reactions have been intensively developed by taking advantage of the highly specific interactions between enzymes and their substrates. In this approach, the peptides or proteins are genetically attached to the target proteins as a tag, and the various labels are then incorporated into the tags by enzyme reactions with the substrates carrying those labels. On the other hand, we have been developing an enzyme-based protein-labeling system distinct from the existing ones. In our system, the substrate protein is attached to the target proteins as a tag, and the labels are incorporated into the tag by post-translational modification with an enzyme carrying those labels followed by tight complexation between the enzyme and the substrate protein. In this review, I summarize the enzyme-based protein-labeling systems with a focus on several typical methods and then describe our labeling system based on tight complexation between the enzyme and the substrate protein.
引用
收藏
页码:156 / 166
页数:11
相关论文
共 65 条
[51]   Spatial separation and bidirectional trafficking of proteins using a multi-functional reporter [J].
Svendsen, Soshana ;
Zimprich, Chad ;
McDougall, Mark G. ;
Klaubert, Dieter H. ;
Los, Georgyi V. .
BMC CELL BIOLOGY, 2008, 9 (1)
[52]   Site-specific protein modification on living cells catalyzed by Sortase [J].
Tanaka, Tsutomu ;
Yamamoto, Teruyasu ;
Tsukiji, Shinya ;
Nagamune, Teruyuki .
CHEMBIOCHEM, 2008, 9 (05) :802-807
[53]   Fluorescent Labeling of the Nuclear Envelope by Localizing Green Fluorescent Protein on the Inner Nuclear Membrane [J].
Taniyama, Toshiyuki ;
Tsuda, Natsumi ;
Sueda, Shinji .
ACS CHEMICAL BIOLOGY, 2018, 13 (06) :1463-1469
[54]   Sortase-Mediated Ligation: A Gift from Gram-Positive Bacteria to Protein Engineering [J].
Tsukiji, Shinya ;
Nagamune, Teruyuki .
CHEMBIOCHEM, 2009, 10 (05) :787-798
[55]   Establishment of NE asymmetry - targeting of membrane proteins to the inner nuclear membrane [J].
Ungricht, Rosemarie ;
Kutay, Ulrike .
CURRENT OPINION IN CELL BIOLOGY, 2015, 34 :135-141
[56]   A fluorophore ligase for site-specific protein labeling inside living cells [J].
Uttamapinant, Chayasith ;
White, Katharine A. ;
Baruah, Hemanta ;
Thompson, Samuel ;
Fernandez-Suarez, Marta ;
Puthenveetil, Sujiet ;
Ting, Alice Y. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (24) :10914-10919
[57]   Hepta-Mutant Staphylococcus aureus Sortase A (SrtA7m) as a Tool for in Vivo Protein Labeling in Caenorhabditis elegans [J].
Wu, Qin ;
Ploegh, Hidde L. ;
Truttmann, Matthias C. .
ACS CHEMICAL BIOLOGY, 2017, 12 (03) :664-673
[58]   Advances in chemical labeling of proteins in living cells [J].
Yan, Qi ;
Bruchez, Marcel P. .
CELL AND TISSUE RESEARCH, 2015, 360 (01) :179-194
[59]  
Yang GY, 2015, NAT METHODS, V12, P137, DOI [10.1038/NMETH.3207, 10.1038/nmeth.3207]
[60]   Fluorophore Targeting to Cellular Proteins via Enzyme-Mediated Azide Ligation and Strain-Promoted Cycloaddition [J].
Yao, Jennifer Z. ;
Uttamapinant, Chayasith ;
Poloukhtine, Andrei ;
Baskin, Jeremy M. ;
Codelli, Julian A. ;
Sletten, Ellen M. ;
Bertozzi, Carolyn R. ;
Popik, Vladimir V. ;
Ting, Alice Y. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (08) :3720-3728