Abstract

Enzyme mediated addressing (EMA) is a highly specific and easy-to-apply technology for direction and deposition of particles and coatings on surfaces. Key feature of this process is an enzymatic reaction in direct proximity to the surface, which induces the deposition. The technique has previously shown great success in the handling of biological particles. In this study, addressing of non-biological nanoparticles, in particular plastics and metals, is presented. The respective particles are stabilized by an amphiphilic, enzyme-degradable block copolymer, consisting of poly(ethylene glycol) and poly(caprolactone). After contact with the enzyme pseudomonas lipase, the particles are destabilized, due to the loss of the hydrophilic part of the block copolymer. The lipase is therefore immobilized on glass supports. Immobilization is performed via adsorption or covalent bonding to epoxide groups. All deposition experiments show that addressing of individual particles occurs precisely within the predefined areas of enzyme activity. Depending on the material and reaction conditions, intact nanoparticles or coatings from such can be gained. The quintessence of the study is the indifference of the EMA regarding particle materials. From this rationale, the technique offers near unlimited materials compatibility within a precise, easy-to-apply, and upscalable process.

Highlights

  • We previously introduced a novel technology which adapts the architectural skills of enzymes and enables defined deposition of colloidal particles in both a highly specific and easy-to-apply manner: the enzyme mediated addressing (EMA) [7]

  • The first approach closely mimics the casein micelle consists of a hydrophilic and a hydrophobic polymer interconnected by anatural peptide linker

  • Nanoparticles from polymers and metals, namely polystyrene, poly(cyclohexyl acrylate), and silver were successfully deposited on glass supports via the process of enzyme mediated addressing

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Summary

Introduction

Biomimetic abstraction of natural systems has become a guiding principle in many fields of materials science and technology in the desire for truly innovative products with supreme performance [1] This approach is likewise valid in coatings technology the ”bio”-discussion centers here mainly around the utilization of renewable resources as substitutes for petrochemical raw materials. In this concept nature is seen as just another feedstock for chemicals to produce similar products which meet the established product quality and price point. This neglects the immense potential of nature which lies within the biological functionality of natural systems. This class of biological, polymeric catalysts is set apart from any other type of molecule class by its specificity, energy efficiency, and adaptability [2,3]

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