Engineering genetic circuit interactions within and between synthetic minimal cells

被引:166
作者
Adamala, Katarzyna P. [1 ,4 ]
Martin-Alarcon, Daniel A. [2 ]
Guthrie-Honea, Katriona R. [1 ]
Boyden, Edward S. [1 ,2 ,3 ]
机构
[1] MIT, Media Lab, Cambridge, MA 02139 USA
[2] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] MIT, Dept Brain & Cognit Sci, McGovern Inst Brain Res, E25-618, Cambridge, MA 02139 USA
[4] Univ Minnesota, Dept Genet Cell Biol & Dev, 5-128 MCB 420 Washington Ave SE, Minneapolis, MN 55455 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
PROTEIN-SYNTHESIS; ESCHERICHIA-COLI; TIGHT REGULATION; ALPHA-HEMOLYSIN; EXPRESSION; ENCAPSULATION; LIPOSOMES; SYSTEM; ORIGINS; BIOLOGY;
D O I
10.1038/NCHEM.2644
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Genetic circuits and reaction cascades are of great importance for synthetic biology, biochemistry and bioengineering. An open question is how to maximize the modularity of their design to enable the integration of different reaction networks and to optimize their scalability and flexibility. One option is encapsulation within liposomes, which enables chemical reactions to proceed in well-isolated environments. Here we adapt liposome encapsulation to enable the modular, controlled compartmentalization of genetic circuits and cascades. We demonstrate that it is possible to engineer genetic circuit-containing synthetic minimal cells (synells) to contain multiple-part genetic cascades, and that these cascades can be controlled by external signals as well as inter-liposomal communication without crosstalk. We also show that liposomes that contain different cascades can be fused in a controlled way so that the products of incompatible reactions can be brought together. Synells thus enable a more modular creation of synthetic biology cascades, an essential step towards their ultimate programmability.
引用
收藏
页码:431 / 439
页数:9
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