Abstract

There is a rising interest in biotechnology for the compartmentalization of biochemical reactions in water droplets. Several applications, such as the widely used digital PCR, seek to encapsulate a single molecule in a droplet to be amplified. Directed evolution, another technology with growing popularity, seeks to replicate what happens in nature by encapsulating a single gene and the protein encoded by this gene, linking genotype with phenotype. Compartmentalizing reactions in droplets also allows the experimentalist to run millions of different reactions in parallel. Compartmentalization requires a fluid that is immiscible with water and a surfactant to stabilize the droplets. While there are fluids and surfactants on the market that have been used to accomplish encapsulation, there are reported concerns with these. Span® 80, for example, a commonly used surfactant, has contaminants that interfere with various biochemical reactions. Similarly, synthetic fluids distributed by the cosmetic industry allow some researchers to produce experimental results that can be published, but then other researchers fail to reproduce some of these protocols due to the unreliable nature of these products, which are not manufactured with the intent of being used in biotechnology. The most reliable fluids, immiscible with water and suitable for biochemical reactions, are fluorinated fluids. Fluorinated compounds have the peculiar characteristic of being immiscible with water while at the same time not mixing with hydrophobic molecules. This peculiar characteristic has made fluorinated fluids attractive because it seems to be the basis of their being biologically inert. However, commercially available fluorinated fluids have densities between 1.4 to 1.6 g/mL. The higher-than-water density of fluorinated oils complicates handling of the droplets since these would float on the fluid since the water droplets would be less dense. This can cause aggregation and coalescence of the droplets. Here, we report the synthesis, characterization, and use of fluorinated polysiloxane oils that have densities similar to the one of water at room temperature, and when mixed with non-ionic fluorinated surfactants, can produce droplets encapsulating biochemical reactions. We show how droplets in these emulsions can host many biological processes, including PCR, DNA origami, rolling circle amplification (RCA), and Taqman® assays. Some of these use unnatural DNA built from an Artificially Expanded Genetic Information System (AEGIS) with six nucleotide "letters".

Highlights

  • There is a growing interest in the biochemical sciences for the compartmentalization or miniaturization of reactions [1, 2]

  • We report here the synthesis, characterization of polysiloxanes, prepared by ring-opening polymerization under conditions that produce fluids with densities near 1 g/ mL while having enough fluorinated monomers to be able to dissolve non-ionic fluorinated surfactants that enable their use for the encapsulation of biochemical reactions

  • It was taken into consideration that the growth of the polymeric chain must be limited since high molecular weight molecules will increase the viscosity of the fluid

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Summary

Introduction

There is a growing interest in the biochemical sciences for the compartmentalization or miniaturization of reactions [1, 2]. One can amplify an isolated gene in a digital PCR or explore the vast protein sequence space in directed evolution experiments [3] Approaches such as directed evolution and/or high throughput screening require sequence diversity. One way to achieve this compartmentalization and screening is with the use of water-in-oil droplets [4] These “artificial cells" [5, 6] and other compartments have several applications, including drug delivery [7,8,9], enzyme directed evolution [1, 10,11,12,13,14], and models for the origin of life [15,16,17,18,19]. While water-hydrophobe-water systems are analogs of natural cells [20,21,22,23,24,25], simple water-in-oil emulsions are intrinsically easier to assemble and more stable to environmental change (especially heating) as compartment analogs of cells

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