Lipidic liquid crystalline cubic phases for preparation of ATP-hydrolysing enzyme electrodes
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
28961546
DOI
10.1016/j.bios.2017.09.036
PII: S0956-5663(17)30644-9
Knihovny.cz E-resources
- Keywords
- ATPase, Enzyme activity, Lipid cubic phase, Protein biosensor, Sodium potassium pump, Voltammetry,
- MeSH
- Adenosine Triphosphate metabolism MeSH
- Biosensing Techniques methods MeSH
- Enzyme Assays methods MeSH
- Enzymes, Immobilized chemistry metabolism MeSH
- Glycerides chemistry MeSH
- Hydrolysis MeSH
- Liquid Crystals chemistry MeSH
- Models, Molecular MeSH
- Swine MeSH
- Sodium-Potassium-Exchanging ATPase chemistry metabolism MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Adenosine Triphosphate MeSH
- Enzymes, Immobilized MeSH
- Glycerides MeSH
- monoolein MeSH Browser
- Sodium-Potassium-Exchanging ATPase MeSH
The lipidic liquid-crystalline cubic phase (LCP) is a membrane-mimetic material useful for the stabilization and structural analysis of membrane proteins. Here, we focused on the incorporation of the membrane ATP-hydrolysing sodium/potassium transporter Na+/K+-ATPase (NKA) into a monoolein-derived LCP. Small-angle X-ray scattering was employed for the determination of the LCP structure, which was of Pn3m symmetry for all the formulations studied. The fully characterized NKA-LCP material was immobilized onto a glassy carbon electrode, forming a highly stable enzyme electrode and a novel sensing platform. A typical NKA voltammetric signature was monitored via the anodic reaction of tyrosine and tryptophan residues. The in situ enzyme activity evaluation was based on the ability of NKA to transform ATP to ADP and free phosphate, the latter reacting with ammonium molybdate to form the ammonium phosphomolybdate complex under acidic conditions. The square-wave voltammetric detection of phosphomolybdate was performed and complemented with spectrophotometric measurement at 710nm. The anodic voltammetric response, corresponding to the catalytic ATP-hydrolysing function of NKA incorporated into the LCP, was monitored at around + 0.2V vs. Ag/AgCl in the presence or absence of ouabain, a specific NKA inhibitor. NKA incorporated into the LCP retained its ATP-hydrolysing activity for 7 days, while the solubilized protein became practically inactive. The novelty of this work is the first incorporation of NKA into a lipidic cubic phase with consequent enzyme functionality and stability evaluation using voltammetric detection. The application of LCPs could also be important in the further development of new membrane protein electrochemical sensors and enzyme electrodes.
References provided by Crossref.org
Lipid-based liquid crystalline materials in electrochemical sensing and nanocarrier technology