Abstract

We report a new platform technology to systematically assemble droplet interface bilayer (DIB) networks in user-defined 3D architectures from cell-sized droplets using optical tweezers. Our OptiDIB platform is the first demonstration of optical trapping to precisely construct 3D DIB networks, paving the way for the development of a new generation of modular bio-systems.

Highlights

  • We report a new platform technology to systematically assemble droplet interface bilayer (DIB) networks in user-defined 3D architectures from cell-sized droplets using optical tweezers

  • Our optically assembled DIB (OptiDIB) platform is the first demonstration of optical trapping to precisely construct 3D DIB networks, paving the way for the development of a new generation of modular bio-systems

  • There have been advances concerning the development of DIB networks that operate in physiological environments, using micropipetting[13,14] and microfluidic technologies.[34]. This is significant in the context of synthetic biology as it supports the concept that these microdroplet networks could be used to form minimal cells, micro-reactor networks, biological circuits, smart biomaterials and minimal tissues.[8]. To fully realise this goal, it is desirable for DIB generation strategies to have: (i) high spatial and temporal resolution for the manipulation of cell-sized microdroplets (ii) the flexibility to assemble any user-defined network either in 2D or in 3D (iii) the capability of addressing and discriminating between heterogeneous droplets to enable the assembly of complex DIB networks from multiple droplet types

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Summary

Introduction

We report a new platform technology to systematically assemble droplet interface bilayer (DIB) networks in user-defined 3D architectures from cell-sized droplets using optical tweezers. The technique works by supplying lipids to either the water droplets (lipid-in) or the surrounding oil medium (lipid-out) and allowing time for the lipid monomers to assemble at the water–oil interface prior to positioning the microdroplets into contact.[1] To this effect, droplet manipulation has been achieved using a variety of different methods including manually[2] or robotically[3] controlled micromanipulators, compressible PDMS substrates,[4] a/c electrokinetics,[5] and microfluidics.[6]

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