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与GP96相关的肾细胞癌衍生肽的分离与鉴定

Isolation and identification of renal cell carcinoma-derived peptides associated with GP96.

作者信息

Li H-Z, Li C-W, Li C-Y, Zhang B-F, Li L-T, Li J-M, Zheng J-N, Chang J-W

机构信息

Jiangsu Key Laboratory of _Biological Cancer Therapy, Xuzhou Medical College, Huaihai Xi Road, Xuzhou, 221002, PR China.

出版信息

Technol Cancer Res Treat. 2013 Aug;12(4):285-93. doi: 10.7785/tcrt.2012.500326. Epub 2013 Feb 22.

Abstract

We determined the possible associated determinants and analyzed whether gp96-_associated antigenic peptides can be found in renal cell carcinoma (RCC). The gp96-peptide complexes were chromatographically purified from resected tumor tissue of RCC patients. SDS-PAGE and Western blot analysis confirmed gp96 using the gp96 monoclonal antibody, and its concentration was measured using BCA. Approximately 20 to 50 μg gp96-peptide complexes was obtained from 1 g RCC tissue. The mass spectrometry (MS) analysis of the eluted peptides included the initial profiling using matrix-assisted laser desorption/ionization time-of-flight MS. Quadrupole time-of-flight MS combined with the Mascot search engine was used to identify the peptides and find proteins from primary sequence databases. MS analysis results demonstrated that the mass range of peptide associated with gp96 was from 1046.48 to 3501.56 Da. Further research confirmed the sequences of two gp96-associated peptides, namely, LVPLEGWGGNVM and PPVYYVPYVVL. However, the original protein of the two peptides could not be found. The results demonstrated that the gp96-associated peptides are small molecular peptides, and the two peptides are deduced to be RCC-associated peptides. The identified peptides were confirmed to be associated with gp96 using the protocols described above. However, the specificity and relevance of the association to the immunogenicity of gp96 remains to be examined. Further analysis must be accomplished before the findings can be applied in peptide vaccine.

摘要

我们确定了可能的相关决定因素,并分析了肾细胞癌(RCC)中是否能找到与gp96相关的抗原肽。从RCC患者切除的肿瘤组织中通过色谱法纯化gp96 - 肽复合物。使用gp96单克隆抗体通过SDS - PAGE和蛋白质印迹分析来确认gp96,并使用BCA测量其浓度。从1g RCC组织中大约获得20至50μg gp96 - 肽复合物。对洗脱肽段的质谱(MS)分析包括使用基质辅助激光解吸/电离飞行时间质谱进行初始分析。四极杆飞行时间质谱结合Mascot搜索引擎用于鉴定肽段并从一级序列数据库中查找蛋白质。MS分析结果表明,与gp96相关的肽段质量范围为1046.48至3501.56Da。进一步研究证实了两个与gp96相关的肽段序列,即LVPLEGWGGNVM和PPVYYVPYVVL。然而,未能找到这两个肽段的原始蛋白质。结果表明,与gp96相关的肽段是小分子肽,且这两个肽段被推断为RCC相关肽段。使用上述方法证实了鉴定出的肽段与gp96相关。然而, 其与gp96免疫原性关联的特异性和相关性仍有待研究。在这些发现应用于肽疫苗之前,必须完成进一步的分析。

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