Abstract

Flow-based coiled systems, through which a heat transfer fluid (such as glycerol) is pumped, are widely used for thermal stabilization of bioreactors and biosensor cuvettes and cells. Previously, using horseradish peroxidase (HRP) as a model protein, we have demonstrated that the incubation of a protein solution in a flow-based system over coiled pipe with flowing glycerol leads to a change in the adsorption properties of the protein macromolecules. Herein, we have studied the effect of the glycerol flow on the properties of HRP, the solution of which was placed differently: i.e., near either the inflow or the outflow linear sections of the pipe, while the coiled section of the pipe was shielded with a grounded metallic cover. Atomic force microscopy (AFM) has been employed in order to visualize the HRP protein macromolecules adsorbed from its solution onto the mica substrate surface. The quantity of adsorbed protein was estimated based on the AFM data. The enzymatic activity of HRP was estimated by spectrophotometry. We demonstrate that a change in the properties of HRP enzyme was observed after the incubation of its solution near the inflow/outflow linear sections of the pipe with flowing glycerol. Namely, after the incubation of HRP solution near the inflow section, a decrease in the protein adsorption onto mica was observed, but its enzymatic activity remained unchanged in comparison to the control sample. In another case, when the HRP solution was incubated near the outflow section, an increased protein adsorption was observed, while the enzyme exhibited considerably lower activity.

Highlights

  • In the typical Atomic force microscopy (AFM) image, obtained in the control experiment (Figure 2a), one can clearly distinguish compact 1- to 1.2-nm-high objects. These objects can be attributed to horseradish peroxidase (HRP) macromolecules, since no such objects was detected on the surface of a mica substrate incubated in a protein-free buffer

  • This study looks into how glycerol flow through a polymeric pipe affects the properties of a model enzyme protein, the solution of which was placed near either the inflow or the outflow sections of the pipe

  • After the HRP solution was incubated near the pipe inflow, a decreased adsorption of the protein onto mica was observed, being approximately 5.5 times lower than that observed for the control solution incubated far away from the pipe

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Summary

Introduction

In bioreactors and bioanalytical devices, a thermal stabilization of measuring cells and/or reaction vessels is often required to provide optimal process conditions. For this purpose, biosensors and bioreactors can be equipped with flow-based systems with circulating heat transfer fluid [1], such as water, ethylene glycol, glycerol, etc. Glycerol and glycerol-containing solutions can be employed for thermal stabilization [2], since their use allows one to vary the process temperature over a broad range from −43.5 ◦ C [3] to 17 ◦ C [4]. Coiled construction of flow-based systems is a popular technical solution realized in bioanalytical equipment. To achieve optimal heat transfer, the reactor, cuvette, etc. To achieve optimal heat transfer, the reactor, cuvette, etc. is

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