首页> 美国卫生研究院文献>Marine Drugs >Identification Purification and Molecular Characterization of Chondrosin a New Protein with Anti-tumoral Activity from the Marine Sponge Chondrosia Reniformis Nardo 1847
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Identification Purification and Molecular Characterization of Chondrosin a New Protein with Anti-tumoral Activity from the Marine Sponge Chondrosia Reniformis Nardo 1847

机译:软骨苷的鉴定纯化和分子表征一种新的蛋白质具有来自海绵的抗肿瘤活性的新蛋白质肾形肾状尼斯Nardo 1847

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摘要

is a common marine demosponge showing many peculiarities, lacking silica spicules and with a body entirely formed by a dense collagenous matrix. In this paper, we have described the identification of a new cytotoxic protein (chondrosin) with selective activity against specific tumor cell lines, from , collected from the Liguria Sea. Chondrosin was extracted and purified using a salting out approach and molecular weight size exclusion chromatography. The cytotoxic fractions were then characterized by two-dimensional gel electrophoresis and mass spectrometry analysis and matched the results with transcriptome database. The procedure allowed for identifying a full-length cDNA encoding for a 199-amino acids (aa) polypeptide, with a signal peptide of 21 amino acids. The mature protein has a theoretical molecular weight of 19611.12 and an IP of 5.11. Cell toxicity assays showed a selective action against some tumor cell lines (RAW 264.7 murine leukemia cells in particular). Cell death was determined by extracellular calcium intake, followed by cytoplasmic reactive oxygen species overproduction. The in silico modelling of chondrosin showed a high structural homology with the -terminal region of the ryanodine receptor/channel and a short identity with defensin. The results are discussed suggesting a possible specific interaction of chondrosin with the Cav 1.3 ion voltage calcium channel expressed on the target cell membranes.
机译:是一种常见的海洋鼻头,显示许多特殊性,缺乏二氧化硅穗,并且具有完全由致密胶原基质形成的身体。在本文中,我们已经描述了从利叶米收集的特异性肿瘤细胞系具有选择性活性的新细胞毒性蛋白(Chondrosin)。用盐析方法和分子量抑制色谱法提取和纯化核糖苷。然后通过二维凝胶电泳和质谱分析表征细胞毒性级分,并将结果与​​转录组数据库匹配。允许鉴定用于199-氨基酸(AA)多肽的全长cDNA的方法,其中21个氨基酸的信号肽。成熟蛋白质具有19611.12的理论分子量和5.11的IP。细胞毒性测定显示出对某些肿瘤细胞系(特别是Raw 264.7鼠白血病细胞)的选择性作用。细胞死亡通过细胞外钙进气确定,然后是细胞质活性氧物质过量生产。 Chondrosin的Silico建模表现出高结构同源性与瑞尼诺受体/通道的终端区域和与防御素的短同种度。讨论结果表明Chondrosin与在靶细胞膜上表达的CAV 1.3离子电压钙通道的可能的特异性相互作用。

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