Abstract

Animal cells and cell lines, such as HEK-293 cells, are commonly cultured at 37°C. These cells are often used to express recombinant proteins. Having a higher expression level or a higher protein yield is generally desirable. As we demonstrate in this study, dropping culture temperature to 33°C, but not lower, 24 hours after transient transfection in HEK-293S cells will give rise to ~1.5-fold higher expression of green fluorescent protein (GFP) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors. By following the time course of the GFP-expressing cells growing at 37°C and 33°C from 24 hours after transfection (including 19 hours recovery at 37°C in the normal growth medium), we found that a mild hypothermia (i.e., 33°C) reduces the growth rate of HEK-293S cells, while increasing cellular productivity of recombinant proteins. As a result, green cells remain undivided in a longer period of time. Not surprisingly, the property of a recombinant protein expressed in the cells grown at 33°C is unaffected, as shown by the use of AMPA receptors. We further demonstrate with the use of PC12 cells that this method may be especially useful when a recombinant protein is difficult to express using a chemical-based, transient transfection method.

Highlights

  • Human embryonic kidney 293 (HEK-293) cells [1] are a popular mammalian, heterologous expression system for producing recombinant proteins [2]

  • Choosing 30°C would seriously reduce biomass

  • As we have demonstrated in this study, lowering the culture temperature to 33°C 24 hours after transient transfection will give rise to ~1.5-fold higher expression of a recombinant protein, such as green fluorescent protein (GFP) and amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors

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Summary

Introduction

Human embryonic kidney 293 (HEK-293) cells [1] are a popular mammalian, heterologous expression system for producing recombinant proteins [2] These cells can be used either intact or in lipid fragments to study structure and function relationships and pharmacological properties of the membrane proteins that are expressed in these cells. The benefit of using HEK-293 cells for expressing recombinant proteins includes an efficient transfection of plasmid DNAs, faithful translation and processing of proteins [2]. In using these cells for expressing membrane proteins, such as ion channels, a low signal is sometimes observed (e.g., a signal can be current amplitude from electrophysiology or radioactivity from binding experiments).

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