Background: Plasma renin can predict future cardiovascular events as well as the prevalence of chronic renal disease in hypertensive subjects. Ovine angiotensinogen (oANG) is a better substrate for measuring renin concentration through activity assay. Recombinant oANG expressed in cells can be utilized as the substrate while measuring plasma renin. We aim to establish an immunoassay for measuring renin concentration at picomolar level using recombinant oANG.
Material And Methods: Recombinant oANG was expressed in cells and purified to homogeneity. Various concentrations (0-1.5 pM) of recombinant human renin standard were prepared and incubated with recombinant oANG. Renin activity was determined by angiotensin-I specific enzyme-linked immunosorbent assay.
Results: About 4.5 mg of purified recombinant oANG was obtained from 0.5 L of culture. The Michaelis constant and turnover number of human renin with recombinant oANG were 0.16 μM and 0.51 s, respectively. A linear relationship was obtained when renin activity was plotted as a function of renin concentration using recombinant oANG as the renin substrate. Picomolar amounts of renin can be measured from known renin activity using this method.
Conclusion: This study established a novel assay system for measuring renin at picomolar level using cost effective recombinant oANG.
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http://dx.doi.org/10.1016/j.heliyon.2019.e01409 | DOI Listing |
Heliyon
April 2019
Center for Highly Advanced Integration of Nano and Life Sciences, Gifu University (G-CHAIN), 1-1 Yanagido, Gifu, 501-1193, Japan.
Background: Plasma renin can predict future cardiovascular events as well as the prevalence of chronic renal disease in hypertensive subjects. Ovine angiotensinogen (oANG) is a better substrate for measuring renin concentration through activity assay. Recombinant oANG expressed in cells can be utilized as the substrate while measuring plasma renin.
View Article and Find Full Text PDFStruct Dyn
March 2016
Department of Chemistry, Inha University, Incheon 402-751, South Korea.
Homodimeric hemoglobin (HbI) consisting of two subunits is a good model system for investigating the allosteric structural transition as it exhibits cooperativity in ligand binding. In this work, as an effort to extend our previous study on wild-type and F97Y mutant HbI, we investigate structural dynamics of a mutant HbI in solution to examine the role of well-organized interfacial water cluster, which has been known to mediate intersubunit communication in HbI. In the T72V mutant of HbI, the interfacial water cluster in the T state is perturbed due to the lack of Thr72, resulting in two less interfacial water molecules than in wild-type HbI.
View Article and Find Full Text PDFBMC Biotechnol
April 2016
Faculty of Applied Biological Sciences, Gifu University, 1-1 Yanagido, Gifu, 501-1193, Japan.
Background: Angiotensinogen (ANG) is a macromolecular precursor of angiotensin, which regulates blood pressure and electrolyte balance. ANG is specifically cleaved by renin, an aspartic protease, to initiate the angiotensin-processing cascade. Ovine ANG (oANG) from sheep plasma has been shown to be a better substrate for human renin, and it has been used in clinical renin assays.
View Article and Find Full Text PDFChemphyschem
November 2013
Center for Nanomaterials and Chemical Reactions, Institute for Basic Science, Daejeon 305-701 (Republic of Korea), Fax: (+82) 42-350-2810; Department of Chemistry, KAIST, Daejeon 305-701 (Republic of Korea).
The mechanism of a photochemical reaction involves the formation and dissociation of various short-lived species on ultrafast timescales and therefore its characterization requires detailed structural information on the transient species. By making use of a structurally sensitive X-ray probe, time-resolved X-ray liquidography (TRXL) can directly elucidate the structures of reacting molecules in the solution phase and thus determine the comprehensive reaction mechanism with high accuracy. In this work, by performing TRXL measurements at two different wavelengths (400 and 267 nm), the reaction mechanism of I3 (-) photolysis, which changes subtly depending on the excitation wavelength, is elucidated.
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