Literature DB >> 31371493

Building a synthetic mechanosensitive signaling pathway in compartmentalized artificial cells.

James W Hindley1,2,3, Daniela G Zheleva1, Yuval Elani1,2,3, Kalypso Charalambous4, Laura M C Barter1,2, Paula J Booth3,5, Charlotte L Bevan6, Robert V Law1,2, Oscar Ces7,2,3.   

Abstract

To date, reconstitution of one of the fundamental methods of cell communication, the signaling pathway, has been unaddressed in the bottom-up construction of artificial cells (ACs). Such developments are needed to increase the functionality and biomimicry of ACs, accelerating their translation and application in biotechnology. Here, we report the construction of a de novo synthetic signaling pathway in microscale nested vesicles. Vesicle-cell models respond to external calcium signals through activation of an intracellular interaction between phospholipase A2 and a mechanosensitive channel present in the internal membranes, triggering content mixing between compartments and controlling cell fluorescence. Emulsion-based approaches to AC construction are therefore shown to be ideal for the quick design and testing of new signaling networks and can readily include synthetic molecules difficult to introduce to biological cells. This work represents a foundation for the engineering of multicompartment-spanning designer pathways that can be utilized to control downstream events inside an AC, leading to the assembly of micromachines capable of sensing and responding to changes in their local environment.

Entities:  

Keywords:  MscL; artificial cells; nested vesicle; phospholipase A2; signaling pathway

Year:  2019        PMID: 31371493      PMCID: PMC6708380          DOI: 10.1073/pnas.1903500116

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  48 in total

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Authors:  Justin Gullingsrud; Klaus Schulten
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9.  Regulating vesicle bilayer permeability and selectivity via stimuli-triggered polymersome-to-PICsome transition.

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