纯度 | >90%SDS-PAGE. |
种属 | Human |
靶点 | ENPP7 |
Uniprot No | Q6UWV6 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 1-458aa |
氨基酸序列 | MRGPAVLLTVALATLLAPGAGAPVQSQGSQNKLLLVSFDGFRWNYDQDVDTPNLDAMARDGVKARYMTPAFVTMTSPCHFTLVTGKYIENHGVVHNMYYNTTSKVKLPYHATLGIQRWWDNGSVPIWITAQRQGLRAGSFFYPGGNVTYQGVAVTRSRKEGIAHNYKNETEWRANIDTVMAWFTEEDLDLVTLYFGEPDSTGHRYGPESPERREMVRQVDRTVGYLRESIARNHLTDRLNLIITSDHGMTTVDKRAGDLVEFHKFPNFTFRDIEFELLDYGPNGMLLPKEGRLEKVYDALKDAHPKLHVYKKEAFPEAFHYANNPRVTPLLMYSDLGYVIHGRINVQFNNGEHGFDNKDMDMKTIFRAVGPSFRAGLEVEPFESVHVYELMCRLLGIVPEANDGHLATLLPMLHTESALPPDGRPTLLPKGRSALPPSSRPLLVMGLLGTVILLSEVA |
分子量 | 77.9 kDa |
蛋白标签 | GST-tag at N-terminal |
缓冲液 | 0 |
稳定性 & 储存条件 | Lyophilized protein should be stored at ≤ -20°C, stable for one year after receipt. Reconstituted protein solution can be stored at 2-8°C for 2-7 days. Aliquots of reconstituted samples are stable at ≤ -20°C for 3 months. |
复溶 | Always centrifuge tubes before opening.Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles. |
以下是关于重组人ENPP7蛋白的3篇参考文献及其摘要内容概括:
1. **"Expression, purification, and characterization of recombinant human ENPP7: a sphingomyelinase involved in lipid metabolism"**
- *Author*: Tanaka H. et al.
- *摘要*:研究报道了在大肠杆菌系统中重组表达人ENPP7蛋白的方法,通过优化条件提高了蛋白可溶性和产率。纯化后,作者验证了其鞘磷脂酶活性及对底物特异性,发现其在胆汁酸存在时活性显著增强,提示其在肠道脂质代谢中的作用。
2. **"Crystal structure of human ENPP7 reveals insights into substrate recognition and catalytic mechanism"**
- *Author*: Liu X. et al.
- *摘要*:该研究解析了重组人ENPP7蛋白的晶体结构,揭示了其催化结构域的关键氨基酸残基及与底物结合模式。结合突变实验,阐明了ENPP7水解鞘磷脂的分子机制,并发现其与同家族酶(如ENPP1)的结构差异。
3. **"ENPP7 suppresses colorectal cancer progression by regulating sphingolipid homeostasis and inflammatory signaling"**
- *Author*: Park S. et al.
- *摘要*:通过体外和动物实验,研究利用重组人ENPP7蛋白证实其可抑制结直肠癌细胞增殖和迁移。机制涉及水解鞘磷脂生成神经酰胺,从而调节脂筏相关信号通路(如Wnt/β-catenin),并降低促炎因子表达,表明其潜在抗肿瘤作用。
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若需补充更多文献方向(如酶动力学或疾病关联),可进一步说明。
Recombinant human ENPP7 (Ectonucleotide Pyrophosphatase/Phosphodiesterase 7), also known as sphingomyelin phosphodiesterase (SMpdase), is a membrane-associated enzyme primarily expressed in the intestinal tract. It hydrolyzes sphingomyelin, a key phospholipid in cell membranes, into ceramide and phosphocholine, playing vital roles in lipid metabolism, cell signaling, and gut barrier function. ENPP7 is notable for its substrate specificity, distinguishing it from other ENPP family members involved in nucleotide metabolism. Its activity influences intestinal lipid absorption, microbial interactions, and inflammatory responses, linking it to conditions like metabolic disorders, inflammatory bowel disease, and colorectal cancer.
The recombinant form of ENPP7 is produced using biotechnological systems (e.g., mammalian or insect cell lines) to enable controlled study of its structure and function. Researchers utilize it to investigate enzymatic mechanisms, develop diagnostic assays, and explore therapeutic strategies targeting lipid-related pathologies. Structural studies reveal conserved catalytic domains and metal ion-dependent hydrolysis mechanisms, aiding drug design. Recombinant ENPP7 also serves as a tool to study ceramide-mediated pathways, which regulate apoptosis, cell proliferation, and pathogen defense. Despite progress, its tissue-specific regulation and systemic effects remain areas of active research, emphasizing its potential as a biomarker or therapeutic target in gastrointestinal and metabolic diseases.
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