纯度 | >90%SDS-PAGE. |
种属 | Human |
靶点 | PARP14 |
Uniprot No | Q460N5 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 1470-1801aa |
氨基酸序列 | MHHHHHHGGGSPILGYWKIKGLVQPTRLLLEYLEEKYEEHLYERDEGDKW RNKKFELGLEFPNLPYYIDGDVKLTQSMAIIRYIADKHNMLGGCPKERAE ISMLEGAVLDIRYGVSRIAYSKDFETLVDFLSKLPEMLKMFKDRLCHKTY LNGDHVTHPDFMLYDALDVVLYMDPMCLDAFPKLVCFKKRIEAIPQIDKY LKSSKYIAWPLQGWQATFGGGDHPPKSDPENLYFQGGGEFKEYQELNELQ KKLNNISLDHKRPLIKVLGISRDVMQARDEIEAMIKRVRLAKEQESRADC ISEFIEWQYNDNNTSHCFNKMTNLKLEDARREKKKTVDVKINHRHYTVNL NTYTATDTKGHSLSVQRLTKSKVDIPAHWSDKQQNFCVVELLPSDPEYNT VASKFNQTCSHFRIEKIERIQNPDLWNSYQAKKKTMDAKNGQTMNEKQLF HGTDAGSVPHVNRNGFNRSYAGKNAVAYGKGTYFAVNANYSANDTYSRPD ANGRKHVYVRVLTGIYTHGNHSLIVPPSKNPQNPTDLYDTVTDNVHHPSL FVAFYDYQAYPEYLITFRK |
预测分子量 | 67 kDa |
蛋白标签 | His tag N-Terminus |
缓冲液 | PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300. |
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PARP14重组蛋白的3篇参考文献及其摘要概括:
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1. **"Recombinant expression and functional characterization of PARP14 domains"**
*Cohen, M.S. et al. (2015)*
研究报道了PARP14多个结构域的重组表达和纯化方法,分析了其ADP-核糖基转移酶活性,发现C端催化结构域对IL-4信号通路的调控至关重要。
2. **"PARP14 promotes survival of diffuse large B-cell lymphoma cells through STAT6 stabilization"**
*Iwata, T.M. et al. (2016)*
通过重组PARP14蛋白实验,揭示其通过结合并稳定STAT6转录因子,促进B细胞淋巴瘤细胞存活,为靶向治疗提供了依据。
3. **"Structural insights into PARP14 catalysis using a recombinant full-length protein"**
*Vyas, S. et al. (2020)*
利用重组全长PARP14蛋白进行X射线晶体学分析,解析其三维结构,阐明了底物结合口袋的构象变化及催化机制。
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以上文献涵盖PARP14重组蛋白的功能研究、疾病机制及结构解析,均发表于生化学与分子生物学领域权威期刊。如需更多细节,建议通过PubMed或SciHub检索完整文本。
PARP14 (Poly(ADP-ribose) polymerase 14) is a member of the ADP-ribosyltransferase superfamily, which catalyzes the transfer of ADP-ribose units to target proteins, modulating their function. Unlike canonical PARPs involved in DNA repair (e.g., PARP1/2), PARP14 is classified as a mono-ADP-ribosyltransferase (MARylator) and plays roles in diverse cellular processes, including signal transduction, transcriptional regulation, DNA repair, cell death, and immune response. It is particularly noted for its involvement in inflammation, fibrosis, and cancer progression, where it often acts as a co-regulator of oncogenic or anti-inflammatory signaling pathways.
The recombinant PARP14 protein is engineered through molecular cloning to express specific functional domains (e.g., catalytic ADP-ribosyltransferase domain or macrodomains) in heterologous systems like *E. coli* or mammalian cells. This allows researchers to study its enzymatic activity, structure, and interactions in vitro. Structurally, PARP14 contains three N-terminal macrodomains that recognize ADP-ribosylated substrates, a central WWE domain for protein interactions, and a C-terminal catalytic domain responsible for its MARylation activity. Recombinant forms are often used to screen inhibitors, characterize substrate specificity, or explore its role in pathways like STAT6-mediated anti-inflammatory signaling or TGF-β-driven fibrosis.
Interest in PARP14 has grown due to its dual roles in promoting cancer cell survival (e.g., via IL-4/STAT6 signaling in B-cell lymphomas) and suppressing excessive inflammation in autoimmune diseases. Its recombinant protein serves as a critical tool for drug discovery, particularly in developing selective PARP14 inhibitors as potential therapeutics. However, its complex biology—balancing pro- and anti-tumorigenic effects depending on context—underscores the need for precise mechanistic studies using well-characterized recombinant proteins.
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