Kiga Daisuke, Sakamoto Kensaku, Kodama Koichiro, Kigawa Takanori, Matsuda Takayoshi, Yabuki Takashi, Shirouzu Mikako, Harada Yoko, Nakayama Hiroshi, Takio Koji, Hasegawa Yoshinori, Endo Yaeta, Hirao Ichiro, Yokoyama Shigeyuki
RIKEN Genomic Sciences Center, 1-7-22 Suehiro-cho, Tsurumi, Yokohama 230-0045, Japan.
Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):9715-20. doi: 10.1073/pnas.142220099. Epub 2002 Jul 3.
Tyrosyl-tRNA synthetase (TyrRS) from Escherichia coli was engineered to preferentially recognize 3-iodo-L-tyrosine rather than L-tyrosine for the site-specific incorporation of 3-iodo-L-tyrosine into proteins in eukaryotic translation systems. The wild-type TyrRS does not recognize 3-iodo-L-tyrosine, because of the bulky iodine substitution. On the basis of the reported crystal structure of Bacillus stearothermophilus TyrRS, three residues, Y37, Q179, and Q195, in the L-tyrosine-binding site were chosen for mutagenesis. Thirty-four single amino acid replacements and 16 of their combinations were screened by in vitro biochemical assays. A combination of the Y37V and Q195C mutations changed the amino acid specificity in such a way that the variant TyrRS activates 3-iodo-L-tyrosine 10-fold more efficiently than L-tyrosine. This engineered enzyme, TyrRS(V37C195), was tested for use in the wheat germ cell-free translation system, which has recently been significantly improved, and is now as productive as conventional recombinant systems. During the translation in the wheat germ system, an E. coli suppressor tRNA(Tyr) was not aminoacylated by the wheat germ enzymes, but was aminoacylated by the E. coli TyrRS(V37C195) variant with 3-iodo-l-tyrosine. After the use of the 3-iodotyrosyl-tRNA in translation, the resultant uncharged tRNA could be aminoacylated again in the system. A mass spectrometric analysis of the produced protein revealed that more than 95% of the amino acids incorporated for an amber codon were iodotyrosine, whose concentration was only twice that of L-tyrosine in the translation. Therefore, the variant enzyme, 3-iodo-L-tyrosine, and the suppressor tRNA can serve as an additional set orthogonal to the 20 endogenous sets in eukaryotic in vitro translation systems.
对来自大肠杆菌的酪氨酰 - tRNA合成酶(TyrRS)进行改造,使其在真核翻译系统中能优先识别3 - 碘 - L - 酪氨酸而非L - 酪氨酸,从而将3 - 碘 - L - 酪氨酸位点特异性地掺入蛋白质中。野生型TyrRS由于碘取代基团体积较大,无法识别3 - 碘 - L - 酪氨酸。基于已报道的嗜热脂肪芽孢杆菌TyrRS的晶体结构,选择L - 酪氨酸结合位点中的三个残基Y37、Q179和Q195进行诱变。通过体外生化分析筛选了34个单氨基酸替换及其16种组合。Y37V和Q195C突变的组合改变了氨基酸特异性,使得变体TyrRS激活3 - 碘 - L - 酪氨酸的效率比L - 酪氨酸高10倍。这种工程酶TyrRS(V37C195)在最近得到显著改进、现在与传统重组系统一样高效的小麦胚无细胞翻译系统中进行了测试。在小麦胚系统的翻译过程中,大肠杆菌抑制性tRNA(Tyr)不能被小麦胚酶氨酰化,但能被大肠杆菌TyrRS(V37C195)变体用3 - 碘 - L - 酪氨酸氨酰化。在翻译中使用3 - 碘酪氨酰 - tRNA后,产生的无电荷tRNA可在该系统中再次被氨酰化。对产生的蛋白质进行质谱分析表明,为琥珀密码子掺入的氨基酸中超过95%是碘酪氨酸,其在翻译中的浓度仅为L - 酪氨酸的两倍。因此,变体酶、3 - 碘 - L - 酪氨酸和抑制性tRNA可作为真核体外翻译系统中与20种内源性组合正交的另一套组合。