详细说明
- Purity>90%, by SDS-PAGE under reducing conditions and visualized by silver stain
- Endotoxin Level<1.0 EU per 1 μg of the protein by the LAL method.
- ActivityMeasured by its ability to cleave the fluorogenic peptide substrate, SNAPEtide. The specific activity is >85 pmol/min/μg, as measured under the described conditions. See Activity Assay Protocol on www.RnDSystems.com
- SourceE. coli-derived Pro2-Ile403, with an N-terminal Met and 6-His tag
- Accession #
- N-terminal Sequence
AnalysisMet - Predicted Molecular Mass46 kDa
- SDS-PAGE43 kDa, reducing conditions
| 5424-ZN | | |
| Formulation Supplied as a 0.2 μm filtered solution in Tris, NaCl, Glycerol, Brij-30 and DTT. | ||
| Shipping The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below. | ||
| Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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- Assay Buffer: 50 mM HEPES, 0.1% (v/v) Tween® 20, pH 8.0
- Recombinant C. botulinum BoNT-E Light Chain (rBoNT-E LC) (Catalog # 5424-ZN)
- Substrate: SNAPEtide (o-Abz/Dnp) (List Biological Laboratories, Inc., Catalog # 550), 2 mM stock in DMSO
- F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
- Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
- Dilute rBoNT-E LC to 10 µg/mL in Assay Buffer.
- Dilute Substrate to 40 µM in Assay Buffer.
- Load into a black well plate 50 µL of 10 µg/mL of rBoNT-E LC, and start the reaction by adding 50 µL of 40 µM Substrate. Include a Substrate Blank containing Assay Buffer and 40 µM Substrate without rBoNT-E LC.
- Read at excitation and emission wavelengths of 320 nm and 410 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 Abz-Gly (Bachem, Catalog # E-2920).
Per Well:- rBoNT-E LC: 0.5 µg
- Substrate: 20 µM
Botulinum Neurotoxin Type E is one of the seven serotypes of Botulinum Neurotoxins (BoNTs) produced by various strains of Clostridium botulinum (1, 2). BoNTs are synthesized as inactive single chain protein precursors and activated by proteolytic cleavage to generate disulfide-linked two-chain proteins. The 50 kDa light chain contains the catalytic domain, whereas the 100 kDa heavy chain contains an internal translocation domain and a receptor binding domain (3). BoNTs are the most potent protein toxins for humans. As zinc proteases, they cleave SNARE proteins to elicit flaccid paralysis in botulism by blocking acetylcholine release at the neuromuscular junction (2‑4). E. coli-expressed recombinant light chains are active proteases. In the absence of the heavy chains, however, they lack toxicity because they cannot enter into host cells.
- References:
- Campbell K.D. et al. (1993) J. Clin. Microbiol. 31:2255.
- Montecucco, C. and Giampietro, S. (1993) Trends. Biochem. Sci. 18:324.
- Turton, K. et al. (2002) Trends. Biochem. Sci. 27:552.
- Schiavo, G. et al. (2000) Physiol. Rev. 80:717.
- Long Name:Botulinum Neurotoxin Type E Light Chain
- Alternate Names:BoNTE Light Chain; BoNT-E Light Chain
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