Biophysical characterization of highly active recombinantGaussia luciferase expressed in Escherichia coli

May 22, 2018

Title

Biophysical characterization of highly active recombinantGaussia luciferase expressed in Escherichia coli

Author

Tharangani Rathnayaka, Minako Tawa, Shihori Sohya, Masafumi Yohda, Yutaka Kuroda

Year

2010

Journal

Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics

Abstract

Recently, the smallest bioluminescent protein (MW: 19.9 kDa), Gaussia luciferase (GLuc), has been isolated from the marine copepod Gaussia princeps and has attracted much attention as a reporter protein. However, preparation of large quantities of homogeneous natively folded recombinant GLuc appears to be difficult due to its ten cysteines. Here, we report the biophysical characterization of recombinant GLuc expressed using a novel Escherichia coli expression system based on a cold induced expression vector (pCold). Using this system, a large fraction of the protein was expressed in the soluble fraction. GLuc, purified exclusively from the supernatant using nickel affinity chromatography, yielded a large amount of pure GLuc with a native disulfide bond pattern (Soluble-GLuc). Soluble-GLuc had a strong bioluminescence activity and it retained 65% of its activity after 30 min incubation at 95 °C. Soluble-GLuc remained fully folded until 40 °C, as assessed by circular dichroism; and the thermal denaturation curve was S-shaped, indicating a cooperative transition, with a midpoint temperature of 56 °C. These results indicate that both the structure and bioluminescence activity of GLuc remain stable at high temperatures, and they strongly suggest GLuc's potential as a reporter protein.

Instrument

FP-6500

Keywords

Fluorescence, Protein folding, Biochemistry