The molten-globule residual structure is critical for reflavination of glucose oxidase
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
28887045
DOI
10.1016/j.bpc.2017.08.009
PII: S0301-4622(17)30317-4
Knihovny.cz E-resources
- Keywords
- Deflavination, Hofmeister anions, Homodimeric interface, Thermal stability,
- MeSH
- Aspergillus niger enzymology MeSH
- Biocatalysis MeSH
- Circular Dichroism MeSH
- Calorimetry, Differential Scanning MeSH
- Flavin-Adenine Dinucleotide chemistry metabolism MeSH
- Glucose Oxidase chemistry metabolism MeSH
- Protein Multimerization MeSH
- Protein Isoforms chemistry metabolism MeSH
- Protein Structure, Secondary MeSH
- Spectrophotometry, Ultraviolet MeSH
- Protein Stability MeSH
- Temperature MeSH
- Protein Structure, Tertiary MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Flavin-Adenine Dinucleotide MeSH
- Glucose Oxidase MeSH
- Protein Isoforms MeSH
Glucose oxidase (GOX) is a homodimeric glycoprotein with tightly bound one molecule of FAD cofactor per monomer of the protein. GOX has numerous applications, but the preparation of biotechnologically interesting GOX sensors requires a removal of the native FAD cofactor. This process often leads to unwanted irreversible deflavination and, as a consequence, to the low enzyme recovery. Molecular mechanisms of reversible reflavination are poorly understood; our current knowledge is based only on empiric rules, which is clearly insufficient for further development. To develop conceptual understanding of flavin-binding competent states, we studied the effect of deflavination protocols on conformational properties of GOX. After deflavination, the apoform assembles into soluble oligomers with nearly native-like holoform secondary structure but largely destabilized tertiary structure presumambly due to the packing density defects around the vacant flavin binding site. The reflavination is cooperative but not fully efficient; after the binding the flavin cofactor, the protein directly disassembles into native homodimers while the fraction of oligomers remains irreversibly inactivated. Importantly, the effect of Hofmeister salts on the conformational properties of GOX and reflavination efficiency indicates that the native-like residual tertiary structure in the molten-globule states favorably supports the reflavination and minimizes the inactivated oligomers. We interpret our results by combining the ligand-induced changes in quaternary structure with salt-sensitive, non-equilibrated conformational selection model. In summary, our work provides the very first steps toward molecular understanding the complexity of the GOX reflavination mechanism.
Department of Biochemistry University of Zurich Winterthurerstrasse 190 CH 8057 Zurich Switzerland
Department of Biophysics P J Šafárik University in Košice Jesenná 5 04154 Košice Slovakia
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