Department of Chemistry, The University of Chicago, 929 E. 57th Street, Chicago, IL, 60637, USA.
Chembiochem. 2019 Jun 14;20(12):1547-1553. doi: 10.1002/cbic.201800707. Epub 2019 Apr 17.
T7 RNA polymerase (RNAP) is a powerful protein scaffold for the construction of synthetic biology tools and biosensors. However, both T7 RNAP and its split variants are intolerant to C-terminal modifications or fusions, thus placing a key limitation on their engineering and deployment. Here, we use rapid continuous-evolution approaches to evolve both full-length and split T7 RNAP variants that tolerate modified C termini and fusions to entire other proteins. Moreover, we show that the evolved split C-terminal RNAP variants can function as small-molecule biosensors, even in the context of large C-terminal fusions. This work provides a panel of modified RNAP variants with robust activity and tolerance to C-terminal fusions, and provides insights into the biophysical requirements of the C-terminal carboxylic acid functional group of T7 RNAP.
T7 RNA 聚合酶(RNAP)是构建合成生物学工具和生物传感器的强大蛋白质支架。然而,T7 RNAP 及其分裂变体都不能容忍 C 末端修饰或融合,因此对它们的工程和部署构成了关键限制。在这里,我们使用快速连续进化方法来进化全长和分裂的 T7 RNAP 变体,这些变体可以容忍修饰的 C 末端和与整个其他蛋白质的融合。此外,我们表明,进化的分裂 C 末端 RNAP 变体可以作为小分子生物传感器发挥作用,即使在大的 C 末端融合的情况下也是如此。这项工作提供了一组具有强大活性和对 C 末端融合耐受性的修饰 RNAP 变体,并深入了解 T7 RNAP 的 C 末端羧酸官能团的生物物理要求。