Photoactive Yellow Protein-Based Protein Labeling System with Turn-On Fluorescence Intensity

被引:105
作者
Hori, Yuichiro [1 ]
Ueno, Hideki [1 ]
Mizukami, Shin [1 ]
Kikuchi, Kazuya [1 ]
机构
[1] Osaka Univ, Grad Sch Engn, Div Adv Sci & Biotechnol, Suita, Osaka 5650871, Japan
关键词
RESONANCE ENERGY-TRANSFER; IN-VITRO;
D O I
10.1021/ja904800k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Protein labeling provides significant information about protein function. In this research, we developed a novel protein labeling technique by utilizing photoactive yellow protein (PYP). PYP is a small protein (14 kDa) derived from purple bacteria and binds to 7-hydroxycoumarin-3-carboxylic acid as well as to a natural ligand, 4-hydroxycinnamic acid, through a thioester bond with Cys69. Based on the structure and fluorescence property of this coumarin derivative, we designed two fluorescent I probes that bind to PYP. One has an azido moiety, which allows stepwise labeling by click chemistry, and the other is a fluorogenic probe. The live-cell imaging and specific labeling of PYP were achieved by using both probes. The flexibility of the probe design and the small size of the tag protein are great advantages of this system against the existing methods. This novel labeling technique can be used in a wide variety of applications for biological research.
引用
收藏
页码:16610 / +
页数:4
相关论文
共 21 条
[1]   New biarsenical Ligands and tetracysteine motifs for protein labeling in vitro and in vivo: Synthesis and biological applications [J].
Adams, SR ;
Campbell, RE ;
Gross, LA ;
Martin, BR ;
Walkup, GK ;
Yao, Y ;
Llopis, J ;
Tsien, RY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (21) :6063-6076
[2]   Short hydrogen bonds in photoactive yellow protein [J].
Anderson, S ;
Crosson, S ;
Moffat, K .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2004, 60 :1008-1016
[3]   Site-specific labeling of proteins with small molecules in live cells [J].
Chen, I ;
Ting, AY .
CURRENT OPINION IN BIOTECHNOLOGY, 2005, 16 (01) :35-40
[4]   Redirecting lipoic acid ligase for cell surface protein labeling with small-molecule probes [J].
Fernandez-Suarez, Marta ;
Baruah, Hemanta ;
Martinez-Hernandez, Laura ;
Xie, Kathleen T. ;
Baskin, Jeremy M. ;
Bertozzi, Carolyn R. ;
Ting, Alice Y. .
NATURE BIOTECHNOLOGY, 2007, 25 (12) :1483-1487
[5]   An engineered protein tag for multiprotein labeling in living cells [J].
Gautier, Arnaud ;
Juillerat, Alexandre ;
Heinis, Christian ;
Correa, Ivan Reis, Jr. ;
Kindermann, Maik ;
Beaufils, Florent ;
Johnsson, Kai .
CHEMISTRY & BIOLOGY, 2008, 15 (02) :128-136
[6]   RECONSTITUTION PHOTOACTIVE YELLOW PROTEIN FROM APOPROTEIN AND P-COUMARIC ACID-DERIVATIVES [J].
IMAMOTO, Y ;
ITO, T ;
KATAOKA, M ;
TOKUNAGA, F .
FEBS LETTERS, 1995, 374 (02) :157-160
[7]   Identification of six new photoactive yellow proteins - Diversity and structure-function relationships in a bacterial blue light photoreceptor [J].
Kumauchi, Masato ;
Hara, Miwa T. ;
Stalcup, Page ;
Xie, Aihua ;
Hoff, Wouter D. .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 2008, 84 (04) :956-969
[8]   Characterization of a bacterial tyrosine ammonia lyase, a biosynthetic enzyme for the photoactive yellow protein [J].
Kyndt, JA ;
Meyer, TE ;
Cusanovich, MA ;
Van Beeumen, JJ .
FEBS LETTERS, 2002, 512 (1-3) :240-244
[9]  
Los GV, 2007, METH MOL B, V356, P195
[10]   Covalent Protein Labeling Based on Noncatalytic β-Lactamase and a Designed FRET Substrate [J].
Mizukami, Shin ;
Watanabe, Shuji ;
Hori, Yuichiro ;
Kikuchi, Kazuya .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (14) :5016-+