化学
电子转移
光诱导电子转移
绿色荧光蛋白
光化学
电子受体
铁氧还蛋白
荧光
发色团
氧化还原
700页
费斯特共振能量转移
生物物理学
电子传输链
电子供体
光系统I
生物化学
光系统II
酶
光合作用
基因
物理
有机化学
量子力学
生物
催化作用
作者
Xiaoxuan Lv,Yang Yu,Meng Zhou,Cheng Hu,Feng Gao,Jiasong Li,Xiaohong Liu,Kai Deng,Peng Zheng,Weimin Gong,Andong Xia,Jiangyun Wang
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 (FNO2Phe), 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 A0. This genetically encoded, low-reduction potential unnatural amino acid (UAA) can significantly improve our ability to investigate electron transfer mechanisms in complex reductases and facilitate the design of miniature proteins that mimic their functions.
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