Direct charging of tRNACUA with pyrrolysine in vitro and in vivo

被引:195
作者
Blight, SK
Larue, RC
Mahapatra, A
Longstaff, DG
Chang, E
Zhao, G
Kang, PT
Church-Church, KB
Chan, MK
Krzycki, JA
机构
[1] Ohio State Univ, Dept Microbiol, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Chem, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Biochem, Columbus, OH 43210 USA
[4] Ohio State Univ, Biochem Program, Columbus, OH 43210 USA
[5] Ohio State Univ, CCIC Mass Spectrometry & Proteom Facil, Columbus, OH 43210 USA
关键词
D O I
10.1038/nature02895
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pyrrolysine is the 22nd amino acid(1-3). An unresolved question has been how this atypical genetically encoded residue is inserted into proteins, because all previously described naturally occurring aminoacyl-tRNA synthetases are specific for one of the 20 universally distributed amino acids. Here we establish that synthetic L-pyrrolysine is attached as a free molecule to tRNA(CUA) by PylS, an archaeal class II aminoacyl-tRNA synthetase. PylS activates pyrrolysine with ATP and ligates pyrrolysine to tRNA(CUA) in vitro in reactions specific for pyrrolysine. The addition of pyrrolysine to Escherichia coli cells expressing pylT (encoding tRNA(CUA)) and pylS results in the translation of UAG in vivo as a sense codon. This is the first example from nature of direct aminoacylation of a tRNA with a non-canonical amino acid and shows that the genetic code of E. coli can be expanded to include UAG-directed pyrrolysine incorporation into proteins.
引用
收藏
页码:333 / 335
页数:3
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