Ultrafast Photoinduced Electron Transfer in Green Fluorescent Protein Bearing a Genetically Encoded Electron Acceptor

被引:23
|
作者
Lv, Xiaoxuan [1 ,2 ]
Yu, Yang [4 ]
Zhou, Meng [3 ]
Hu, Cheng [1 ,2 ]
Gao, Feng [1 ,2 ]
Li, Jiasong [1 ,2 ]
Liu, Xiaohong [1 ,2 ]
Deng, Kai [1 ,2 ]
Zheng, Peng [1 ,2 ]
Gong, Weimin [1 ,2 ]
Xia, Andong [3 ]
Wang, Jiangyun [1 ,2 ]
机构
[1] Chinese Acad Sci, Lab RNA Biol, Inst Biophys, Beijing 100101, Peoples R China
[2] Chinese Acad Sci, Lab Quantum Biophys, Inst Biophys, Beijing 100101, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Beijing 100190, Peoples R China
[4] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
关键词
EXCITED-STATE DYNAMICS; PHOTOSYSTEM-II; VARIANT S65T/H148D; COUPLED ELECTRON; ENERGY-TRANSFER; IRON-SULFUR; AMINO-ACID; REDUCTION; COPPER; FLOW;
D O I
10.1021/jacs.5b03652
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electron transfer (ET) is widely used for driving the processes that underlie the chemistry of life. However, our abilities to probe electron transfer mechanisms in proteins and design redox enzymes are limited, due to :the lack of methods to site-specifically insert electron acceptors into proteins in vivo. Here we describe the synthesis and genetic incorporation of 4-fluoro-3-nitrophenylalanine (FNO(2)Phe), which has similar reduction potentials to NAD(P)H and ferredoxin, the most important biological reductants. Through the genetic incorporation of FNO2Phe into green fluorescent:protein (GFP) and femtosecond transient absorption measurement, we show that photoinduced electron transfer (PET) from the GFP chromophore to FNO2Phe occurs very fast (within 11 ps), which is comparable to that of the first electron transfer step in photosystem I, from P700* to A(0). This genetically encoded, low-reduction potential unnatural amino acid (UAA) can significantly in-Trove our ability to investigate electron transfer mechanisms in complex reductases and facilitate the design of miniature proteins that mimic their functions.
引用
收藏
页码:7270 / 7273
页数:4
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