Duca Maria, Chen Shengxi, Hecht Sidney M
Departments of Chemistry and Biology, University of Virginia, Charlottesville, VA 22904, USA.
Methods. 2008 Feb;44(2):87-99. doi: 10.1016/j.ymeth.2007.10.007.
The detailed synthesis of (bis)aminoacyl-pdCpAs and the corresponding singly and tandemly activated tRNAs is reported. The synthetic pathway leading to these compounds has been validated for simple amino acid residues as well as for amino acids bearing more complex side chains. Protection/deprotection strategies are described. For the bisaminoacylated tRNAs, both the synthesis of tRNAs bearing the same amino acid residue at the 2' and 3' positions and tRNAs bearing two different aminoacyl moieties are reported. Further, it is shown that the tandemly activated tRNAs are able to participate in protein synthesis.
报道了(双)氨基酰化-pdCpA以及相应的单激活和串联激活tRNA的详细合成过程。导致这些化合物的合成途径已针对简单氨基酸残基以及带有更复杂侧链的氨基酸进行了验证。描述了保护/去保护策略。对于双氨基酰化tRNA,报道了在2'和3'位置带有相同氨基酸残基的tRNA以及带有两个不同氨基酰部分的tRNA的合成。此外,结果表明串联激活的tRNA能够参与蛋白质合成。