Human Recombinant CASP1 protein, His Tag (V2LY-0526-LY2597)

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Basic Information

Expressed Host
E. coli
Protein Species
Human
Tag
His Tag
Protein Construction
This product is Human Recombinant CASP1 protein, His Tag consist of Amino Acid: 120-404 and predicts a molecular mass of 33.01 kDa.
Molecule Mass
33.01 kDa
Sequence
Amino Acid: 120-404
Species
Human

Formulations & Storage [For reference only, actual COA shall prevail!]

Purity
≥80% as determined by SDS-PAGE.
Endotoxin
Please contact us for more information.
Format
Lyophilized
Reconstitution
Allow the vial and reconstitution buffer to equilibrate to room temperature. Briefly centrifuge or tap down the vial to ensure that all lyophilized powder is collected at the bottom of the vial. For the reconstitution of this product, we recommend adding PBS or sterile water to achieve a final antibody concentration of 1 mg/mL. Allow the vial to reconstitute for 10-15 minutes at room temperature with gentle agitation. Avoid vigorous shaking that can cause foaming and antibody denaturation. Aliquot into volumes based on your experiment and store liquid protein at -20°C or -80°C for long time.
Buffer
Lyophilized from sterile PBS
Preservative
None
Storage
Samples are stable for up to twelve months from date of receipt at -20°C to -80°C. Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
More Infomation

Target

Full Name
Caspase 1
Function
Thiol protease involved in a variety of inflammatory processes by proteolytically cleaving other proteins, such as the precursors of the inflammatory cytokines interleukin-1 beta (IL1B) and interleukin 18 (IL18) as well as the pyroptosis inducer Gasdermin-D (GSDMD), into active mature peptides (PubMed:15326478, PubMed:1574116, PubMed:7876192, PubMed:15498465, PubMed:26375003, PubMed:32051255).
Plays a key role in cell immunity as an inflammatory response initiator: once activated through formation of an inflammasome complex, it initiates a proinflammatory response through the cleavage of the two inflammatory cytokines IL1B and IL18, releasing the mature cytokines which are involved in a variety of inflammatory processes (PubMed:1574116, PubMed:7876192, PubMed:15498465, PubMed:15326478, PubMed:32051255).
Cleaves a tetrapeptide after an Asp residue at position P1 (PubMed:1574116, PubMed:7876192, PubMed:15498465).
Also initiates pyroptosis, a programmed lytic cell death pathway, through cleavage of GSDMD (PubMed:26375003).
In contrast to cleavage of interleukins IL1B and IL1B, recognition and cleavage of GSDMD is not strictly dependent on the consensus cleavage site but depends on an exosite interface on CASP1 that recognizes and binds the Gasdermin-D, C-terminal (GSDMD-CT) part (PubMed:32051255, PubMed:32109412, PubMed:32553275).
Upon inflammasome activation, during DNA virus infection but not RNA virus challenge, controls antiviral immunity through the cleavage of CGAS, rendering it inactive (PubMed:28314590).
In apoptotic cells, cleaves SPHK2 which is released from cells and remains enzymatically active extracellularly (PubMed:20197547).
Isoform Delta: Apoptosis inactive.
Isoform Epsilon: Apoptosis inactive.
Biological Process
Apoptotic process Source: ProtInc
Cellular response to cytokine stimulus Source: Reactome
Cellular response to interferon-gamma Source: UniProtKB
Cellular response to lipopolysaccharide Source: UniProtKB
Cellular response to mechanical stimulus Source: UniProtKB
Cellular response to organic substance Source: MGI
Cytokine-mediated signaling pathway Source: Reactome
Cytokine precursor processing Source: ARUK-UCL
Execution phase of apoptosis Source: GOC
Membrane hyperpolarization Source: Ensembl
Mitochondrial depolarization Source: Ensembl
Positive regulation of cysteine-type endopeptidase activity involved in apoptotic process Source: UniProtKB
Positive regulation of I-kappaB kinase/NF-kappaB signaling Source: UniProtKB
Positive regulation of interleukin-1 alpha production Source: Ensembl
Positive regulation of interleukin-1 beta production Source: UniProtKB
Positive regulation of tumor necrosis factor-mediated signaling pathway Source: UniProtKB
Programmed necrotic cell death Source: Ensembl
Protein autoprocessing Source: UniProtKB
Proteolysis Source: UniProtKB
Purinergic nucleotide receptor signaling pathway Source: Reactome
Pyroptosis Source: UniProtKB
Regulation of apoptotic process Source: Reactome
Regulation of autophagy Source: Ensembl
Regulation of inflammatory response Source: UniProtKB
Response to ATP Source: Ensembl
Response to hypoxia Source: Ensembl
Signaling receptor ligand precursor processing Source: ARUK-UCL
Signal transduction Source: ProtInc
Toxin transport Source: Ensembl
Cellular Location
Cell membrane; Cytoplasm
PTM
The two subunits are derived from the precursor sequence by an autocatalytic mechanism.
Ubiquitinated via 'Lys-11'-linked polyubiquitination. Deubiquitinated by USP8.
Cleavage in the interdomain linker region is required to induce pyroptosis.

Zeng, X., Luo, X., Mao, X., Wen, D., Zhang, H., & Wang, J. (2021). Inflammatory and immune-related factor Caspase 1 contributes to the development of oral lichen planus. Archives of Oral Biology, 131, 105244.

Flores, J., Noël, A., Fillion, M. L., & LeBlanc, A. C. (2021). Therapeutic potential of Nlrp1 inflammasome, Caspase-1, or Caspase-6 against Alzheimer disease cognitive impairment. Cell Death & Differentiation, 1-13.

Crowley, S. M., Han, X., Allaire, J. M., Stahl, M., Rauch, I., Knodler, L. A., & Vallance, B. A. (2020). Intestinal restriction of Salmonella Typhimurium requires caspase-1 and caspase-11 epithelial intrinsic inflammasomes. PLoS pathogens, 16(4), e1008498.

Reinke, S., Linge, M., Diebner, H. H., Luksch, H., Glage, S., Gocht, A., ... & Winkler, S. (2020). Non-canonical caspase-1 signaling drives RIP2-dependent and TNF-α-mediated inflammation in vivo. Cell reports, 30(8), 2501-2511.

Wooff, Y., Fernando, N., Wong, J. H., Dietrich, C., Aggio-Bruce, R., Chu-Tan, J. A., ... & Natoli, R. (2020). Caspase-1-dependent inflammasomes mediate photoreceptor cell death in photo-oxidative damage-induced retinal degeneration. Scientific reports, 10(1), 1-20.

Kapplusch, F., Schulze, F., Rabe-Matschewsky, S., Russ, S., Herbig, M., Heymann, M. C., ... & Hofmann, S. R. (2019). CASP1 variants influence subcellular caspase-1 localization, pyroptosome formation, pro-inflammatory cell death and macrophage deformability. Clinical Immunology, 208, 108232.

Gonçalves, A. V., Margolis, S. R., Quirino, G. F., Mascarenhas, D. P., Rauch, I., Nichols, R. D., ... & Zamboni, D. S. (2019). Gasdermin-D and Caspase-7 are the key Caspase-1/8 substrates downstream of the NAIP5/NLRC4 inflammasome required for restriction of Legionella pneumophila. PLoS pathogens, 15(6), e1007886.

Chang, I., Mitsui, Y., Kim, S. K., Sun, J. S., Jeon, H. S., Kang, J. Y., ... & Tanaka, Y. (2017). Cytochrome P450 1B1 inhibition suppresses tumorigenicity of prostate cancer via caspase-1 activation. Oncotarget, 8(24), 39087.

Man, S. M., Karki, R., Briard, B., Burton, A., Gingras, S., Pelletier, S., & Kanneganti, T. D. (2017). Differential roles of caspase-1 and caspase-11 in infection and inflammation. Scientific reports, 7(1), 1-11.

Mascarenhas, D. P., Cerqueira, D. M., Pereira, M. S., Castanheira, F. V., Fernandes, T. D., Manin, G. Z., ... & Zamboni, D. S. (2017). Inhibition of caspase-1 or gasdermin-D enable caspase-8 activation in the Naip5/NLRC4/ASC inflammasome. PLoS pathogens, 13(8), e1006502.

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For research use only. Not intended for any clinical use.

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