Saito Hirohide, Minamisawa Tamiko, Shiba Kiyotaka
Department of Protein Engineering, Cancer Institute, Japanese Foundation for Cancer Research, Koto-ku, Tokyo, Japan.
Nucleic Acids Res. 2007;35(6):e38. doi: 10.1093/nar/gkm017. Epub 2007 Feb 7.
The presence of peptide motifs within the proteins provides the synthetic biologist with the opportunity to fabricate novel proteins through the programming of these motifs. Here we describe a method that enables one to combine multiple peptide motifs to generate a combinatorial protein library. With this method, a set of sense and antisense oligonucleotide primers were prepared. These primers were mixed and polymerized, so that the resultant DNA consisted of combinatorial polymers of multiple microgenes created from the stochastic assembly of the sense and antisense primers. With this motif-mixing method, we prepared a protein library from the BH1-4 motifs shared among Bcl-2 family proteins. Among the 41 clones created, 70% of clones had a stable, presumably folded expression product in human cells, which was detectable by immunohistochemistry and western blot. The proteins obtained varied with respect to both the number and the order of the four motifs. The method enables homology-independent polymerization of DNA blocks that coded motif sequences, and the frequency of each motif within a library can be adjusted in a tailor-made manner. This motif programming has a potential for creating a library with a large proportion of folded/functional proteins.
蛋白质中肽基序的存在为合成生物学家提供了通过对这些基序进行编程来制造新型蛋白质的机会。在此,我们描述了一种能够将多个肽基序组合以生成组合蛋白质文库的方法。利用该方法,制备了一组正义和反义寡核苷酸引物。将这些引物混合并聚合,使得所得DNA由通过正义和反义引物的随机组装产生的多个微基因的组合聚合物组成。通过这种基序混合方法,我们从Bcl-2家族蛋白共有的BH1-4基序制备了一个蛋白质文库。在产生的41个克隆中,70%的克隆在人细胞中具有稳定的、可能折叠的表达产物,可通过免疫组织化学和蛋白质印迹检测到。所获得的蛋白质在四个基序的数量和顺序方面均有所不同。该方法能够对编码基序序列的DNA片段进行不依赖同源性的聚合,并且文库中每个基序的频率可以定制调整。这种基序编程有潜力创建一个包含大量折叠/功能蛋白的文库。