Recombinant Human Dopa Decarboxylase/DDC Protein, CF Summary
Details of Functionality
Measured by its ability to convert the substrate 3, 4-dihydroxy L-phenylalanine (L-Dopa) to 3, 4-dihydroxyphenylethylamine (dopamine). The dopamine product is measured by its absorbance at 340 nm after derivatization with trinitrobenzene sulfonic acid. Sherald, F. et al. (1973) Anal. Biochem. 56:300. The specific activity is >1500 pmol/min/µg, as measured under the described conditions.
Source
Spodoptera frugiperda, Sf 21 (baculovirus)-derived human Dopa Decarboxylase/DDC protein Met1-Glu480, with a C-terminal 6-His tag
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Enzyme Activity
Theoretical MW
55 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
55 kDa, reducing conditions
Publications
Read Publication using 3564-DC in the following applications:
96 well clear UV-transparent microplate (Corning, Catalog # 3635)
Plate Reader (Model: Spectramax Plus by Molecular Devices) or equivalent
Prepare 5 mM stock solutions of L-DOPA and pyridoxal phosphate in deionized water. Use vigorous vortexing and mixing to get both reagents into solution.
Dilute rhDopa to 5 ng/µL in Assay Buffer.
Combine 160 µL of 5 ng/μL rhDopa with 20 µL 5 mM L-DOPA, 4 µL 5 mM pyridoxal phosphate, and 16 µL Assay Buffer. Include a control containing 20 µL 5 mM L-DOPA, 4 µL 5 mM pyridoxal phosphate, and 176 µL Assay Buffer without any rhDopa.
Incubate for 30 minutes at 37 °C.
Stop the reaction by heating for 2 minutes at 95 - 100 °C. After heating, cool on ice.
Add 10 µL of 5% TNBS to each tube and vortex.
Incubate for 20 minutes at 37 °C. Ensure that all samples undergo derivitization for the same length of time, stagger the addition of TNBS and the benzene extraction (next step) if necessary.
In a fume hood, add 300 µL of benzene to each reaction in the same order the 5% TNBS was added. Vortex for 30 seconds.
Centrifuge all reactions at 13,000 rpm in a microcentrifuge for 5 minutes to separate the aqueous and organic solvents.
Carefully pipet out 200 µL of the benzene phase (the upper layer) of each reaction and load into a UV-transparent microplate. It is recommended that the microplate be kept covered as much as possible to minimize evaporation of the benzene.
Read at an absorbance of 340 nm in endpoint mode.
Calculate specific activity:
Specific Activity (pmol/min/µg) =
Adjusted Abs* (OD) x Conversion Factor** (pmol/OD)
Incubation time (min) x amount of enzyme (µg)
*Adjusted for Substrate Blank
**Derived using calibration standard dopamine (3,4-dihydroxyphenylethylamine) (Sigma, Catalog # H8502).
Per Reaction:
rhDopa: 0.800 µg
L-DOPA: 500 µM
Pyridoxal Phosphate: 100 µM
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Dopa Decarboxylase/DDC Protein, CF
Dopa Decarboxylase (DDC), also known as aromatic amino acid decarboxylase, is a group II decarboxylase (1). The enzyme catalyzes the decarboxylation of aromatic L-amino acids to produce the corresponding amines. DDC produces the neurotransmitters dopamine and serotonin from L-Dopa and L-5-hydroxytryptophan, respectively. The inhibition of DDC could be used for the treatment of schizophrenia and Parkinson's disease (2).
Sandmeier, E. et al. (1994) Eur. J. Biochem. 221:997.
Bertoldi, M. et al. (1996) J. Biol. Chem. 271:23954.
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