Ueda Takuya, Kanamori Takashi, Ohashi Hiroyuki
The Department of Medical Genome Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Chiba, Japan.
Methods Mol Biol. 2010;607:219-25. doi: 10.1007/978-1-60327-331-2_18.
The ribosome display utilizes the formation of the mRNA-ribosome-polypeptide ternary complex in the cell-free protein synthesis system as the linking of the genotype (mRNA) to the phenotype (polypeptide). However, the presence of intrinsic components such as nucleases in the cell-extract based cell-free protein synthesis systems inevitably reduces the stability of the ternary complex, which would prevent attainment of reliable results. We have developed an efficient and highly controllable ribosome display system using the Protein synthesis Using Recombinant Elements (PURE) system. The mRNA-ribosome-polypeptide ternary complex is highly stable in the PURE system and then the selected mRNA can be easily recovered, because activities of nucleases and other inhibitory factors are very low in the PURE system. Furthermore, omission of the release factors within the original PURE system can aid stalling of the ribosome at the termination codon to form the mRNA-ribosome-polypeptide ternary complex. We believe that these advantages assure the usability of the modified PURE system for ribosome display.
核糖体展示利用无细胞蛋白质合成系统中mRNA-核糖体-多肽三元复合物的形成,将基因型(mRNA)与表型(多肽)联系起来。然而,基于细胞提取物的无细胞蛋白质合成系统中存在诸如核酸酶等内在成分,不可避免地会降低三元复合物的稳定性,这会妨碍获得可靠的结果。我们利用重组元件蛋白质合成(PURE)系统开发了一种高效且高度可控的核糖体展示系统。mRNA-核糖体-多肽三元复合物在PURE系统中高度稳定,然后可以轻松回收所选的mRNA,因为PURE系统中核酸酶和其他抑制因子的活性非常低。此外,在原始PURE系统中省略释放因子有助于核糖体在终止密码子处停滞,从而形成mRNA-核糖体-多肽三元复合物。我们相信这些优势确保了改良后的PURE系统在核糖体展示中的可用性。