journal article·2019-06-19Open access

Design of Sealable Custom-Shaped Cell Mimicries Based on Self-Assembled Monolayers on CYTOP Polymer

Hiromune Eto, Naoki Soga, Henri G. Franquelim, Philipp Glock, Alena Khmelinskaia, Lei Kai, Michael Heymann, Hiroyuki Noji, Petra Schwille

ACS Applied Materials & Interfaces· Volume 11· Issue 24

Abstract

In bottom-up synthetic biology, one of the major methodological challenges is to provide reaction spaces that mimic biological systems with regard to topology and surface functionality. Of particular interest are cell- or organelle-shaped membrane compartments, as many protein functions unfold at lipid interfaces. However, shaping artificial cell systems using materials with non-intrusive physicochemical properties, while maintaining flexible lipid interfaces relevant to the reconstituted protein systems, is not straightforward. Herein, we develop micropatterned chambers from CYTOP, a less commonly used polymer with good chemical resistance and a refractive index matching that of water. By forming a self-assembled lipid monolayer on the polymer surface, we dramatically increased the biocompatibility of CYTOP-fabricated systems. The phospholipid interface provides an excellent passivation layer to prevent protein adhesion to the hydrophobic surface, and we succeeded in cell-free protein synthesis inside the chambers. Importantly, the chambers could be sealed after loading by a lipid monolayer, providing a novel platform to study encapsulated systems. We successfully reconstituted pole-to-pole oscillations of the Escherichia coli MinDE system, which responds dramatically to compartment geometry. Furthermore, we present a simplified fabrication of our artificial cell compartments via replica molding, making it a readily accessible technique for standard cleanroom facilities.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Lipid Membrane Structure and Behavior · Microfluidic and Bio-sensing Technologies · Nanopore and Nanochannel Transport Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Max Planck Institute of Biochemistry, Am Klopferspitz 18, D-82152 Martinsried, Germany

Department of Applied Chemistry, Graduate School of Engineering, The University of Tokyo, Bunkyo-ku, Tokyo 113-8656, Japan

Institute for Protein Design, University of Washington, Seattle 98195, Washington, United States

School of Life Sciences, Jiangsu Normal University, Shanghai Road 101, 221116 Xuzhou, P. R. China

Funding

Bundesministerium f?r Bildung und Forschung · Deutsche Forschungsgemeinschaft · Core Research for Evolutional Science and Technology · Japan Science and Technology Agency · Japan Society for the Promotion of Science · Max-Planck-Gesellschaft · Graduate School of Quantitative Biosciences Munich · International Max Planck Research School for Molecular Life Sciences

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