Tokyo Institute of Technology, Graduate School of Life Science and Technology, 4259-R1-18 Nagatsuta-cho, Midori-ku, Yokohama 226-8503, Kanagawa, Japan.
Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259-R1-18 Nagatsuta-cho, Midori-ku, Yokohama 226-8503, Kanagawa, Japan.
Sensors (Basel). 2021 Jul 22;21(15):4993. doi: 10.3390/s21154993.
With the widespread application of recombinant DNA technology, many useful substances are produced by bioprocesses. For the monitoring of the recombinant protein production process, most of the existing technologies are those for the culture environment (pH, O, etc.). However, the production status of the target protein can only be known after the subsequent separation and purification process. To speed up the monitoring of the production process and screening of the higher-yield target protein variants, here we developed an antibody-based His-tag sensor Quenchbody (Q-body), which can quickly detect the C-terminally His-tagged recombinant protein produced in the culture medium. Compared with single-chain Fv-based Q-body having one dye, the Fab-based Q-body having two dyes showed a higher response. In addition, not only was fluorescence response improved but also detection sensitivity by the mutations of tyrosine to tryptophan in the heavy chain CDR region. Moreover, the effect of the mutations on antigen-binding was successfully validated by molecular docking simulation by CDOCKER. Finally, the constructed Q-body was successfully applied to monitor the amount of anti-SARS CoV-2 nanobody secreted into the culture media.
随着重组 DNA 技术的广泛应用,许多有用的物质都是通过生物工艺生产的。为了监测重组蛋白的生产过程,现有的大多数技术都是针对培养环境(pH、O 等)的。然而,只有在随后的分离和纯化过程之后,才能了解目标蛋白的生产状况。为了加快生产过程的监测和筛选高产目标蛋白变体,我们在这里开发了一种基于抗体的 His 标签传感器 Quenchbody(Q-body),它可以快速检测到培养基中产生的 C 端 His 标记的重组蛋白。与基于单链 Fv 的具有一个染料的 Q-body 相比,基于 Fab 的具有两个染料的 Q-body 表现出更高的响应。此外,通过重链 CDR 区域中酪氨酸突变为色氨酸,不仅提高了荧光响应,还提高了检测灵敏度。此外,通过 CDOCKER 的分子对接模拟成功验证了突变对抗原结合的影响。最后,成功地将构建的 Q-body 应用于监测抗 SARS-CoV-2 纳米抗体分泌到培养基中的量。