Genetic encoding of a highly photostable, long lifetime fluorescent amino acid for imaging in mammalian cells

被引:34
作者
Jones, Chloe M. [1 ,2 ]
Robkis, D. Miklos [1 ,2 ]
Blizzard, Robert J. [3 ]
Munari, Mika [4 ]
Venkatesh, Yarra [1 ]
Mihaila, Tiberiu S. [1 ]
Eddins, Alex J. [3 ]
Mehl, Ryan A. [3 ]
Zagotta, William N. [4 ]
Gordon, Sharona E. [4 ]
Petersson, E. James [2 ]
机构
[1] Univ Penn, Dept Chem, 231 South 34th St, Philadelphia, PA 19104 USA
[2] Univ Penn, Biochem & Mol Biophys Grad Grp, 3700 Hamilton Walk, Philadelphia, PA 19104 USA
[3] Oregon State Univ, Dept Biochem & Biophys, 2011 Ag Life Sci Bldg, Corvallis, OR 97331 USA
[4] Univ Washington, Dept Physiol & Biophys, 1705 NE Pacific St,Box 357290, Seattle, WA 98195 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
TRANSFER-RNA SYNTHETASE; ALPHA-SYNUCLEIN; LABELING PROTEINS; CODE EXPANSION; FRET; MUTAGENESIS; MOLECULES; EVOLUTION; PLATFORM; SYSTEM;
D O I
10.1039/d1sc01914g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Acridonylalanine (Acd) is a fluorescent amino acid that is highly photostable, with a high quantum yield and long fluorescence lifetime in water. These properties make it superior to existing genetically encodable fluorescent amino acids for monitoring protein interactions and conformational changes through fluorescence polarization or lifetime experiments, including fluorescence lifetime imaging microscopy (FLIM). Here, we report the genetic incorporation of Acd using engineered pyrrolysine tRNA synthetase (RS) mutants that allow for efficient Acd incorporation in both E. coli and mammalian cells. We compare protein yields and amino acid specificity for these Acd RSs to identify an optimal construct. We also demonstrate the use of Acd in FLIM, where its long lifetime provides strong contrast compared to endogenous fluorophores and engineered fluorescent proteins, which have lifetimes less than 5 ns.
引用
收藏
页码:11955 / 11964
页数:11
相关论文
共 74 条
[1]   Modification of C Terminus Provides New Insights into the Mechanism of α-Synuclein Aggregation [J].
Afitska, Kseniia ;
Fucikova, Anna ;
Shvadchak, Volodymyr V. ;
Yushchenko, Dmytro A. .
BIOPHYSICAL JOURNAL, 2017, 113 (10) :2182-2191
[2]   Live Cell Imaging of Bioorthogonally Labelled Proteins Generated With a Single Pyrrolysine tRNA Gene [J].
Aloush, Noa ;
Schvartz, Tomer ;
Konig, Andres I. ;
Cohen, Sarit ;
Brozgol, Eugene ;
Tam, Benjamin ;
Nachmias, Dikla ;
Ben-David, Oshrit ;
Garini, Yuval ;
Elia, Natalie ;
Arbely, Eyal .
SCIENTIFIC REPORTS, 2018, 8
[3]  
[Anonymous], 2015, The PyMOL Molecular Graphics System
[4]   Photocontrol of Tyrosine Phosphorylation in Mammalian Cells via Genetic Encoding of Photocaged Tyrosine [J].
Arbely, Eyal ;
Torres-Kolbus, Jessica ;
Deiters, Alexander ;
Chin, Jason W. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (29) :11912-11915
[5]   Inteins as Traceless Purification Tags for Unnatural Amino Acid Proteins [J].
Batjargal, Solongo ;
Walters, Christopher R. ;
Petersson, E. James .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (05) :1734-1737
[6]   Native Chemical Ligation of Thioamide-Containing Peptides: Development and Application to the Synthesis of Labeled α-Synuclein for Misfolding Studies [J].
Batjargal, Solongo ;
Wang, Yanxin J. ;
Goldberg, Jacob M. ;
Wissner, Rebecca F. ;
Petersson, E. James .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (22) :9172-9182
[7]   An Evolved Methanomethylophilus alvus Pyrrolysyl-tRNA Synthetase/tRNA Pair Is Highly Active and Orthogonal in Mammalian Cells [J].
Beranek, Vaclav ;
Willis, Julian C. W. ;
Chin, Jason W. .
BIOCHEMISTRY, 2019, 58 (05) :387-390
[8]   Fluorescence Lifetime Measurements and Biological Imaging [J].
Berezin, Mikhail Y. ;
Achilefu, Samuel .
CHEMICAL REVIEWS, 2010, 110 (05) :2641-2684
[9]  
Brand S, 2018, METHODS MOL BIOL, V1728, P327, DOI 10.1007/978-1-4939-7574-7_21
[10]   Peak emission wavelength and fluorescence lifetime are coupled in far-red, GFP-like fluorescent proteins [J].
Canty, Laura ;
Hariharan, Santosh ;
Liu, Qian ;
Haney, Steven A. ;
Andrews, David W. .
PLOS ONE, 2018, 13 (11)