scholarly journals Directed evolution of GFP with non-natural amino acids identifies residues for augmenting and photoswitching fluorescence

2015 ◽  
Vol 6 (2) ◽  
pp. 1159-1166 ◽  
Author(s):  
Samuel C. Reddington ◽  
Amy J. Baldwin ◽  
Rebecca Thompson ◽  
Andrea Brancale ◽  
Eric M. Tippmann ◽  
...  

Genetic code reprogramming allows proteins to sample new chemistry through targeted introduction of non-natural amino acids. By combining with random codon replacement, residues traditionally overlooked can be identified as instilling new properties on a target protein.

2019 ◽  
Vol 17 (25) ◽  
pp. 6127-6130
Author(s):  
Hui Miao ◽  
Chenguang Yu ◽  
Anzhi Yao ◽  
Weimin Xuan

Genetic code expansion depends on the directed evolution of aaRS to recognize non-canonical amino acids. Herein, we reported a function-based method that enables rapidly evolving aaRS for acylated lysine derivatives.


2008 ◽  
Vol 105 (46) ◽  
pp. 17688-17693 ◽  
Author(s):  
Chang C. Liu ◽  
Antha V. Mack ◽  
Meng-Lin Tsao ◽  
Jeremy H. Mills ◽  
Hyun Soo Lee ◽  
...  

We have devised a phage display system in which an expanded genetic code is available for directed evolution. This system allows selection to yield proteins containing unnatural amino acids should such sequences functionally outperform ones containing only the 20 canonical amino acids. We have optimized this system for use with several unnatural amino acids and provide a demonstration of its utility through the selection of anti-gp120 antibodies. One such phage-displayed antibody, selected from a naïve germline scFv antibody library in which six residues in VH CDR3 were randomized, contains sulfotyrosine and binds gp120 more effectively than a similarly displayed known sulfated antibody isolated from human serum. These experiments suggest that an expanded “synthetic” genetic code can confer a selective advantage in the directed evolution of proteins with specific properties.


2006 ◽  
Vol 1 (6) ◽  
pp. 2957-2962 ◽  
Author(s):  
Nobumasa Hino ◽  
Akiko Hayashi ◽  
Kensaku Sakamoto ◽  
Shigeyuki Yokoyama

2011 ◽  
Vol 411 (4) ◽  
pp. 757-761 ◽  
Author(s):  
Takahito Mukai ◽  
Tatsuo Yanagisawa ◽  
Kazumasa Ohtake ◽  
Masatoshi Wakamori ◽  
Jiro Adachi ◽  
...  

1982 ◽  
Vol 47 (1) ◽  
pp. 210-216 ◽  
Author(s):  
Milan Strašák ◽  
František Bachratý ◽  
Jaroslav Majer

The synthesis and physico-chemical parameters are described of a new complexone based on natural amino acids, viz. ethylenediamine-N,N'-di-S-α-isovalerate (SS-EDDIV). 1H- and 13C-NMR data revealed that the methyl group in the substance are not equivalent. The isomers of the cobalt(III) complex with the asymmetric tetradentate SS-EDDIV ligand were prepared and separated; their characteristics are given. The absolute configuration of two of the five theoretically feasible isomers was determined based on their electronic absorption spectra and circular dichroism data.


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