Tabuchi Ichiro, Soramoto Sayaka, Ueno Shingo, Husimi Yuzuru
Tokyo Evolution Research Center, 1-1-45-504, Okubo, Shinjuku-ku, Tokyo 169-0072, Japan.
BMC Biotechnol. 2004 Sep 1;4:19. doi: 10.1186/1472-6750-4-19.
We developed a method to make a various high quality random peptide libraries for evolutionary protein engineering based on a combinatorial DNA synthesis.
A split synthesis in codon units was performed with mixtures of bases optimally designed by using a Genetic Algorithm program. It required only standard DNA synthetic reagents and standard DNA synthesizers in three lines. This multi-line split DNA synthesis (MLSDS) is simply realized by adding a mix-and-split process to normal DNA synthesis protocol. Superiority of MLSDS method over other methods was shown. We demonstrated the synthesis of oligonucleotide libraries with 1016 diversity, and the construction of a library with random sequence coding 120 amino acids containing few stop codons.
Owing to the flexibility of the MLSDS method, it will be able to design various "rational" libraries by using bioinformatics databases.
我们开发了一种基于组合DNA合成制备用于进化蛋白质工程的各种高质量随机肽库的方法。
使用遗传算法程序优化设计的碱基混合物以密码子单位进行拆分合成。该方法仅需要标准DNA合成试剂和三台标准DNA合成仪。这种多线路拆分DNA合成(MLSDS)通过在常规DNA合成方案中添加混合与拆分过程即可简单实现。结果表明MLSDS方法优于其他方法。我们展示了多样性为1016的寡核苷酸库的合成,以及具有编码120个氨基酸且几乎不含终止密码子的随机序列文库的构建。
由于MLSDS方法的灵活性,它将能够通过使用生物信息学数据库设计各种“合理的”文库。