Difference between revisions of "Part:BBa K2986004"
Line 20: | Line 20: | ||
[[File:Hgluc with il8 flow.png|450px|thumb|left|Figjre2.hGluc flow and Il8 flow]] | [[File:Hgluc with il8 flow.png|450px|thumb|left|Figjre2.hGluc flow and Il8 flow]] | ||
− | [[File:HGlu secretion and IL8 elisa.png|450px|thumb| | + | [[File:HGlu secretion and IL8 elisa.png|450px|thumb|right|Figjre3.hGluc secretion and Il8 Elisa]] |
We use the hGluc to be a quantity that characterize the the level of secretion the cytokine Interleukin 8. We can see from the curve that the tendency of the hGluc is similiar to the secertion of the Il8. This shows our plasmid works will in transfering the hGluc-bound cytokine expression system into the target cells. | We use the hGluc to be a quantity that characterize the the level of secretion the cytokine Interleukin 8. We can see from the curve that the tendency of the hGluc is similiar to the secertion of the Il8. This shows our plasmid works will in transfering the hGluc-bound cytokine expression system into the target cells. | ||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
Line 29: | Line 34: | ||
<partinfo>BBa_K2986004 parameters</partinfo> | <partinfo>BBa_K2986004 parameters</partinfo> | ||
<!-- --> | <!-- --> | ||
+ | |||
+ | |||
+ | |||
+ | |||
===Design Notes=== | ===Design Notes=== |
Revision as of 07:53, 7 October 2019
hGluc
Usage and Biology
The luciferase from the marine copepod Gaussia princeps (Gluc) is the smallest (∼19.9-kDa) coelenterazine (CTZ)-utilizing luciferase known thus far. A humanized variant of Gluc (hGluc), which was codon optimized for expression in cultured mammalian cells, has been widely used as a reporter gene. Gaussia luciferase exhibits an activity up to 1,000-fold higher than to Renilla reniformis luciferase (Rluc), firefly luciferase (Fluc), or bacterial luciferases (LuxAB). The outstanding sensitivity of Gluc-based assays was previously demonstrated detecting as low as 10−18 mol purified Gluc or one eukaryotic cell transiently expressing Gluc.
we use the plamid contains the hGluc, mRuby to be a quantity that characterize the the level of secretion the cytokine Il8. Interleukin 8 (IL8 or chemokine (C-X-C motif) ligand 8, CXCL8) is a chemokine produced by macrophages and other cell types such as epithelial cells, airway smooth muscle cells and endothelial cells. Endothelial cells store IL-8 in their storage vesicles, the Weibel-Palade bodies. In humans, the interleukin-8 protein is encoded by the CXCL8 gene. IL-8 is initially produced as a precursor peptide of 99 amino acids which then undergoes cleavage to create several active IL-8 isoforms.In culture, a 72 amino acid peptide is the major form secreted by macrophages.
There are many receptors on the surface membrane capable of binding IL-8; the most frequently studied types are the G protein-coupled serpentine receptors CXCR1 and CXCR2. Expression and affinity for IL-8 differs between the two receptors (CXCR1 > CXCR2). Through a chain of biochemical reactions, IL-8 is secreted and is an important mediator of the immune reaction in the innate immune system response.
IL-8, also known as neutrophil chemotactic factor, has two primary functions. It induces chemotaxis in target cells, primarily neutrophils but also other granulocytes, causing them to migrate toward the site of infection. IL-8 also stimulates phagocytosis once they have arrived. IL-8 is also known to be a potent promoter of angiogenesis. In target cells, IL-8 induces a series of physiological responses required for migration and phagocytosis, such as increases in intracellular Ca2+, exocytosis (e.g. histamine release), and the respiratory burst.
IL-8 can be secreted by any cells with toll-like receptors that are involved in the innate immune response. Usually, it is the macrophages that see an antigen first, and thus are the first cells to release IL-8 to recruit other cells. Both monomer and homodimer forms of IL-8 have been reported to be potent inducers of the chemokine receptors CXCR1 and CXCR2. The homodimer is more potent, but methylation of Leu25 can block the activity of homodimers.
Experiment
We use the hGluc to be a quantity that characterize the the level of secretion the cytokine Interleukin 8. We can see from the curve that the tendency of the hGluc is similiar to the secertion of the Il8. This shows our plasmid works will in transfering the hGluc-bound cytokine expression system into the target cells.
Design Notes
how to use the hGluc to represent the cytokine expression.
Source
Snapgene
References
[1].Tannous B. A. (2009). Gaussia luciferase reporter assay for monitoring biological processes in culture and in vivo. Nature protocols, 4(4), 582–591. doi:10.1038/nprot.2009.28.
[2].Hedges JC, Singer CA, Gerthoffer WT (2000). "Mitogen-activated protein kinases regulate cytokine gene expression in human airway myocytes". Am. J. Respir. Cell Mol. Biol. 23 (1): 86–94. CiteSeerX 10.1.1.326.6212. doi:10.1165/ajrcmb.23.1.4014. PMID 10873157.
[3].Brat DJ, Bellail AC, Van Meir EG (2005). "The role of interleukin-8 and its receptors in gliomagenesis and tumoral angiogenesis". Neuro-oncology. 7 (2): 122–133. doi:10.1215/s1152851704001061. PMC 1871893. PMID 15831231.
[4].Utgaard JO, Jahnsen FL, Bakka A, Brandtzaeg P, Haraldsen G (1998). "Rapid secretion of prestored interleukin 8 from Weibel-Palade bodies of microvascular endothelial cells". J. Exp. Med. 188 (9): 1751–6. doi:10.1084/jem.188.9.1751. PMC 2212514. PMID 9802986.
[5].Modi WS, Dean M, Seuanez HN, Mukaida N, Matsushima K, O'Brien SJ (1990). "Monocyte-derived neutrophil chemotactic factor (MDNCF/IL-8) resides in a gene cluster along with several other members of the platelet factor 4 gene superfamily". Hum. Genet. 84 (2): 185–7. doi:10.1007/BF00208938. PMID 1967588.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 604