A scalable peptide-GPCR language for engineering multicellular communication

被引:41
作者
Billerbeck, Sonja [1 ]
Brisbois, James [1 ]
Agmon, Neta [2 ,3 ]
Jimenez, Miguel [1 ,5 ]
Temple, Jasmine [2 ,3 ]
Shen, Michael [2 ,3 ]
Boeke, Jef D. [2 ,3 ]
Cornish, Virginia W. [1 ,4 ]
机构
[1] Columbia Univ, Dept Chem, New York, NY 10027 USA
[2] NYU Langone Hlth, Inst Syst Genet, 430 East 29th St, New York, NY 10016 USA
[3] NYU Langone Hlth, Dept Biochem & Mol Pharmacol, 430 East 29th St, New York, NY 10016 USA
[4] Columbia Univ, Dept Syst Biol, New York, NY 10032 USA
[5] MIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
关键词
CELL-CELL COMMUNICATION; SACCHAROMYCES-CEREVISIAE; BIOSYNTHESIS; INTERFERENCE; SYSTEMS;
D O I
10.1038/s41467-018-07610-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Engineering multicellularity is one of the next breakthroughs for Synthetic Biology. A key bottleneck to building multicellular systems is the lack of a scalable signaling language with a large number of interfaces that can be used simultaneously. Here, we present a modular, scalable, intercellular signaling language in yeast based on fungal mating peptide/G-protein-coupled receptor (GPCR) pairs harnessed from nature. First, through genome-mining, we assemble 32 functional peptide-GPCR signaling interfaces with a range of dose-response characteristics. Next, we demonstrate that these interfaces can be combined into two-cell communication links, which serve as assembly units for higher-order communication topologies. Finally, we show 56 functional, two-cell links, which we use to assemble three-to six-member communication topologies and a three-member interdependent community. Importantly, our peptide-GPCR language is scalable and tunable by genetic encoding, requires minimal component engineering, and should be massively scalable by further application of our genome mining pipeline or directed evolution.
引用
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页数:12
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