Abstract
Human thyroid peroxidase (hTPO) has been secretory expressed in AD293 mammalian cells. cDNA sequence of 'Gluc' (Gaussia luciferase) protein from Gaussia princeps was incorporated at the amino terminal of hTPO gene for secretion of targeted protein outside the mammalian cells. Augmentation of TPO clone in serum free mediums was investigated and a simplified purification procedure of hTPO has been reported here. Purified hTPO was further analyzed by SDS-PAGE and immunoblotting (western blotting). The relative molecular mass of hTPO was found to be 105kDa. This is the first report with respect to cost effective and simplified purification approach to get highest yield and purity of recombinant hTPO.
Keywords:
Augmentation; Gaussia luciferase; Recombinant hTPO protein.
Copyright © 2017 Elsevier B.V. All rights reserved.
MeSH terms
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Amino Acid Sequence
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Autoantigens / genetics
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Autoantigens / isolation & purification*
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Cell Line
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Chromatography, Ion Exchange / methods
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Cloning, Molecular
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Gene Expression
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Genes, Reporter
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Genetic Vectors / chemistry*
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Genetic Vectors / metabolism
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HEK293 Cells
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Humans
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Iodide Peroxidase / genetics
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Iodide Peroxidase / isolation & purification*
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Iodide Peroxidase / metabolism
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Iron-Binding Proteins / genetics
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Iron-Binding Proteins / isolation & purification*
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Iron-Binding Proteins / metabolism
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Kinetics
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Luciferases / genetics*
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Luciferases / metabolism
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Recombinant Fusion Proteins / genetics
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Recombinant Fusion Proteins / isolation & purification*
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Recombinant Fusion Proteins / metabolism
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Sequence Alignment
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Sequence Homology, Amino Acid
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Transfection
Substances
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Autoantigens
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Iron-Binding Proteins
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Recombinant Fusion Proteins
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TPO protein, human
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Iodide Peroxidase
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Luciferases