Van Raad Damian, Huber Thomas
Research School of Chemistry, Australian National University, Canberra, ACT 2601, Australia.
ACS Synth Biol. 2021 May 21;10(5):1237-1244. doi: 10.1021/acssynbio.1c00044. Epub 2021 May 10.
A novel cell free protein synthesis (CFPS) system utilizing layer-by-layer (LbL) polymer assembly was developed to reduce the operational cost of conventional CFPS. This yielded an encapsulated cell system, dubbed "eCells", that successfully performs CFPS and allows cost-effective incorporation of noncanonical amino acids into proteins. The use of eCells in CFPS circumvents the need for traditional cell lysate preparation and purification of amino acyl-tRNA synthetases (aaRS) while still retaining the small scale of an reaction. eCells were found to be 55% as productive as standard dialysis CFPS at 13% of the cost. The reaction was shown to be scalable over a large range of reaction volumes, and the crowding environment in eCells confers a stabilizing effect on marginally stable proteins, such as the pyrrolysl tRNA synthetase (PylRS), providing a means for their application in protein expression. Photocaged-cysteine (PCC) and -(-butoxycarbonyl)-l-lysine (Boc-lysine) were incorporated into Peptidyl-prolyl cis-trans isomerase B (PpiB) using small amounts of ncAA with an adequate yield of protein. Fluorescent activated cell sorting (FACS) was used to demonstrate the partition of the lysate within the eCells in contrast to standard one pot cell lysate-based methods.
一种利用层层(LbL)聚合物组装的新型无细胞蛋白质合成(CFPS)系统被开发出来,以降低传统CFPS的运营成本。这产生了一种被称为“e细胞”的封装细胞系统,该系统成功地进行了CFPS,并允许将非天然氨基酸经济高效地掺入蛋白质中。在CFPS中使用e细胞避免了传统细胞裂解液制备和氨基酰-tRNA合成酶(aaRS)纯化的需要,同时仍保持小规模反应。研究发现,e细胞的生产效率是标准透析CFPS的55%,而成本仅为其13%。该反应在大范围的反应体积内都可扩展,并且e细胞中的拥挤环境对边缘稳定的蛋白质,如吡咯赖氨酸tRNA合成酶(PylRS)具有稳定作用,为其在蛋白质表达中的应用提供了一种方法。使用少量非天然氨基酸将光笼化半胱氨酸(PCC)和N-(叔丁氧羰基)-L-赖氨酸(Boc-赖氨酸)掺入肽基脯氨酰顺反异构酶B(PpiB)中,蛋白质产量充足。与基于标准单罐细胞裂解液的方法相比,荧光激活细胞分选(FACS)被用于证明裂解液在e细胞内的分配情况。