Shape and Size Control of Artificial Cells for Bottom-Up Biology

Journal Article (2019)
Author(s)

Federico Fanalista (TU Delft - BN/Cees Dekker Lab, Kavli institute of nanoscience Delft)

Anthony Birnie (Kavli institute of nanoscience Delft, TU Delft - BN/Cees Dekker Lab)

Renu Maan (Kavli institute of nanoscience Delft, TU Delft - BN/Marileen Dogterom Lab)

Federica Burla (AMOLF Institute for Atomic and Molecular Physics)

Kevin Charles (TU Delft - BN/Cees Dekker Lab, Kavli institute of nanoscience Delft)

Grzegorz Pawlik (Kavli institute of nanoscience Delft, TU Delft - BN/Cees Dekker Lab)

Siddharth Deshpande (TU Delft - BN/Cees Dekker Lab, Kavli institute of nanoscience Delft)

G.H. Koenderink (AMOLF Institute for Atomic and Molecular Physics)

Marileen Dogterom (TU Delft - BN/Bionanoscience, Kavli institute of nanoscience Delft)

Cees Dekker (Kavli institute of nanoscience Delft, TU Delft - BN/Cees Dekker Lab)

Research Group
BN/Cees Dekker Lab
DOI related publication
https://doi.org/10.1021/acsnano.9b00220
More Info
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Publication Year
2019
Language
English
Research Group
BN/Cees Dekker Lab
Journal title
ACS Nano
Issue number
5
Volume number
13
Pages (from-to)
5439-5450
Downloads counter
257
Collections
Institutional Repository
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Abstract

Bottom-up biology is an expanding research field that aims to understand the mechanisms underlying biological processes via in vitro assembly of their essential components in synthetic cells. As encapsulation and controlled manipulation of these elements is a crucial step in the recreation of such cell-like objects, microfluidics is increasingly used for the production of minimal artificial containers such as single-emulsion droplets, double-emulsion droplets, and liposomes. Despite the importance of cell morphology on cellular dynamics, current synthetic-cell studies mainly use spherical containers, and methods to actively shape manipulate these have been lacking. In this paper, we describe a microfluidic platform to deform the shape of artificial cells into a variety of shapes (rods and discs) with adjustable cell-like dimensions below 5 μm, thereby mimicking realistic cell morphologies. To illustrate the potential of our method, we reconstitute three biologically relevant protein systems (FtsZ, microtubules, collagen) inside rod-shaped containers and study the arrangement of the protein networks inside these synthetic containers with physiologically relevant morphologies resembling those found in living cells.