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Building a synthetic mechanosensitive signaling pathway in compartmentalized artificial cells.
Hindley, James W; Zheleva, Daniela G; Elani, Yuval; Charalambous, Kalypso; Barter, Laura M C; Booth, Paula J; Bevan, Charlotte L; Law, Robert V; Ces, Oscar.
Affiliation
  • Hindley JW; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, W12 0BZ London, United Kingdom.
  • Zheleva DG; Institute of Chemical Biology, Imperial College London, Molecular Sciences Research Hub, W12 0BZ London, United Kingdom.
  • Elani Y; FABRICELL, Imperial College London and King's College London, W12 0BZ London, United Kingdom.
  • Charalambous K; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, W12 0BZ London, United Kingdom.
  • Barter LMC; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, W12 0BZ London, United Kingdom.
  • Booth PJ; Institute of Chemical Biology, Imperial College London, Molecular Sciences Research Hub, W12 0BZ London, United Kingdom.
  • Bevan CL; FABRICELL, Imperial College London and King's College London, W12 0BZ London, United Kingdom.
  • Law RV; Department of Bioengineering, Imperial College London, South Kensington, SW7 2AZ London, United Kingdom.
  • Ces O; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, W12 0BZ London, United Kingdom.
Proc Natl Acad Sci U S A ; 116(34): 16711-16716, 2019 08 20.
Article in En | MEDLINE | ID: mdl-31371493
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Compartmentation / Mechanotransduction, Cellular / Artificial Cells Type of study: Prognostic_studies Language: En Journal: Proc Natl Acad Sci U S A Year: 2019 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Compartmentation / Mechanotransduction, Cellular / Artificial Cells Type of study: Prognostic_studies Language: En Journal: Proc Natl Acad Sci U S A Year: 2019 Document type: Article Affiliation country: