Recombinant Cynomolgus Monkey DPPIV/CD26 Protein, CF Summary
| Details of Functionality |
Measured by its ability to cleave the fluorogenic peptide substrate, Gly-Pro-7-amido-4-methylcoumarin (GP-AMC). The specific activity is >3,000 pmol/min/μg, as measured under the described conditions. |
| Source |
Human embryonic kidney cell, HEK293-derived cynomolgus monkey DPPIV/CD26 protein Asn29-Pro766 with a C-terminal 6-His tag |
| Accession # |
|
| N-terminal Sequence |
Asn29 |
| Protein/Peptide Type |
Recombinant Enzymes |
| Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining |
| Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
| Dilutions |
|
| Theoretical MW |
86 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 |
100-116 kDa, reducing conditions |
Packaging, Storage & Formulations
| Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 6 months from date of receipt, -20 to -70 °C as supplied.
- 3 months, -20 to -70 °C under sterile conditions after opening.
|
| Buffer |
Supplied as a 0.2 μm filtered solution in Tris and NaCl. |
| Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining |
| Assay Procedure |
- Assay Buffer: 25 mM Tris, pH 8.0
- Recombinant Cynomolgus Monkey DPPIV/CD26 (rcynoDPPIV) (Catalog # 9637-SE)
- Substrate: H-Gly-Pro-AMC (Bachem, Catalog # I-1225), 10 mM stock in DMSO
- F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
- Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
- Dilute rcynoDPPIV to 0.2 ng/µL in Assay Buffer.
- Dilute Substrate to 20 µM in Assay Buffer.
- Load 50 μL of 0.2 ng/µL rcynoDPPIV into a plate, and start the reaction by adding 50 μL of 20 µM Substrate. For Substrate Blank, load 50 μL of Assay Buffer and 50 μL of Substrate.
- Read at excitation and emission wavelengths of 380 nm and 460 nm (top read), respectively, in kinetic mode for 5 minutes.
- Calculate specific activity:
Specific Activity (pmol/min/µg) = | Adjusted Vmax* (RFU/min) x Conversion Factor** (pmol/RFU) | | amount of enzyme (µg) |
*Adjusted for Substrate Blank. **Derived using calibration standard 7-amino, 4-Methyl Coumarin (Sigma, Catalog # A9891). Per Well: - rcynoDPPIV: 0.010 μg
- Substrate: 10 µM
|
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Cynomolgus Monkey DPPIV/CD26 Protein, CF
Background
DPPIV/CD26 is an approximately 110 kDa serine exopeptidase that releases
Xaa-Pro or Xaa-Ala dipeptides from the N-terminus of oligo- and polypeptides.
It regulates immune and endocrine function through the cleavage of multiple
chemokines, growth factors, and peptide hormones (1, 2). Mature DPPIV
consists of a cytoplasmic tail, a transmembrane
segment, and an extracellular domain (ECD) that contains the catalytic
active site (Ser, Asp, and His charge relay system) (3). Within the ECD, cynoDPPIV/CD26 shares 96% amino acid sequence identity with human DPPIV. DPPIV
is expressed as a nocovalent homodimer on the surface of epithelial cells,
endothelial cells, and activated lymphocytes, and it can be released by MMP mediated
shedding (4). It cleaves a range of peptide hormones including Glucagon, Glucagon-like
Peptides 1 and 2, GIP, GHRH, Procalcitonin, Neuropeptide Y, and Substance P (5).
It is released from adipocytes and induces insulin resistance in adipocytes and
skeletal muscle (6). DPPIV also cleaves many chemokines, resulting in reduced
chemotactic activity of CXCL6, 9, 10, 11, 12, and CCL5 (7-10) but unchanged
angiostatic activity of CXCL9 and CXCL10 (8). Cleavage can increase (CCL5),
decrease (CXCL12), or have no effect (CCL4) on chemokine blockade of HIV-1
cellular infectivity (7, 9, 11). In addition, DPPIV cleavage of CCL4 broadens
chemokine receptor usage to also include CCR2b (11). DPPIV serves as a cell
entry coreceptor for HIV and coronavirus (12, 13). It cleaves human GM-CSF and
IL-3 and reduces their ability to promote myeloid cell development (14). It
also interferes with CXCL12 induced hematopoietic cell migration, homing, and
engraftment (15). DPPIV interacts
in cis
with Adenosine Deaminase on T cells and in
trans with Caveolin-1 on antigen presenting cells (16, 17). It provides
costimulatory proliferation and activation signals to both CD4
+ and CD8
+ T cells (17, 18).
- Klemann, C. et al. (2016) Clin. Exp. Immunol. 185:1.
- Metzemaekers, M. et al. (2016) Front Immunol. 7:483.
- Tanaka, T. et al. (1992) J. Immunol. 149:481.
- Rohrborn, D. et al. (2014) FEBS Lett. 588:3870.
- Waumans, Y. et al. (2015) Front. Immunol. 6:387.
- Lamers, D. et al. (2011) Diabetes 60:1917.
- Proost, P. et al. (1998) J. Biol. Chem. 273:7222.
- Proost, P. et al. (2001) Blood 98:3554.
- Ohtsuki, T. et al. (1998) FEBS Lett. 431:236.
- Barreira da Silva, R. et al. (2015) Nat. Immunol. 16:850.
- Guan, E. et al. (2002) J. Biol. Chem. 277:32348.
- Callebaut, C. et al. (1993) Science 262:2045.
- Raj, V.S. et al. (2013) Nature 495:251.
- Broxmeyer, H.E. et al. (2012) Nat. Med. 18:1786.
- Christopherson II, K.W. et al. (2004) Science 305:1000.
- Kameoka, J. et al. (1993) Science 261:466.
- Ohnuma, K. et al. (2007) J. Biol. Chem. 282:10117.
- Hatano, R. et al. (2013) Immunology 138:165.
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