Tabuchi Ichiro, Soramoto Sayaka, Suzuki Miho, Nishigaki Koichi, Nemoto Naoto, Husimi Yuzuru
Department of Functional Materials Science, Saitama University. 255 Shimo-okubo, Saitama 338-857. Japan.; GenCom Co. 11 Minami-Oya, Machida 194-8511. Japan.Present address: Tokyo Evolution Research Center. 1-1-45-504, Okubo, Shinjuku-ku, Tokyo, 169-0072. Japan.
Biol Proced Online. 2002 Oct 28;4:49-54. doi: 10.1251/bpo33.
The "in vitro virus" is a molecular construct to perform evolutionary protein engineering. The "virion (=viral particle)" (mRNA-peptide fusion), is made by bonding a nascent protein with its coding mRNA via puromycin in a test tube for in vitro translation. In this work, the puromycin-linker was attached to mRNA using the Y-ligation, which was a method of two single-strands ligation at the end of a double-stranded stem to make a stem-loop structure. This reaction gave a yield of about 95%. We compared the Y-ligation with two other ligation reactions and showed that the Y-ligation gave the best productivity. An efficient amplification of the in vitro virus with this "viral genome" was demonstrated.
“体外病毒”是一种用于进行进化蛋白质工程的分子构建体。“病毒粒子(=病毒颗粒)”(mRNA-肽融合体)是通过在试管中利用嘌呤霉素将新生蛋白质与其编码mRNA结合以进行体外翻译而制成的。在这项工作中,使用Y连接法将嘌呤霉素连接子连接到mRNA上,Y连接法是在双链茎的末端进行两条单链连接以形成茎环结构的方法。该反应的产率约为95%。我们将Y连接法与其他两种连接反应进行了比较,结果表明Y连接法具有最佳的生产效率。利用这种“病毒基因组”对体外病毒进行了高效扩增。