Key Laboratory of Advanced Textile Materials and Manufacturing Technology, Ministry of Education, Zhejiang Sci-Tech University, Hangzhou 310018, China.
Key Scientific Research Base of Textile Conservation, State Administration for Cultural Heritage, China National Silk Museum, Hangzhou 310002, China.
J Proteomics. 2019 Oct 30;209:103510. doi: 10.1016/j.jprot.2019.103510. Epub 2019 Aug 31.
Achieving efficient identification of silk protein requires highly sensitive analytical techniques and favorable extraction methods, which is of great significance to the research of ancient silk, especially for the controversial issue of the silk origin. In this paper, proteomics and western blot were proposed to analyze the silk proteins of Bombyx mori (B. mori) and Antheraea pernyi (A. pernyi) dissolved by different methods. First, the differences in secondary structure were detected via spectroscopy. LC-MS/MS was then employed to characterize the peptides of silk proteins precisely. LiBr solution exhibited outstanding dissolution effect on B. mori cocoon, with 87 proteins detected; while copper-ethylenediamine solution (CED) was more appropriate for A. pernyi cocoon, and 16 proteins were identified in A. pernyi-CED. In addition to fibroin and sericin, abundant seroins, enzymes, protease inhibitors, other functional proteins and uncharacterized proteins were detected. Based on the LC-MS/MS data, diagnostic antibodies for the two species were prepared, and fibroin was successfully identified by western blot assay because both dissolution methods were gentle and did not destroy the antigenic epitopes in the protein molecule. Owing to their good specificity and high sensitivity, these diagnostic antibodies have good application prospects in immunoassays of different silk species. SIGNIFICANCE: This study presents the comprehensive analysis on silk identification of proteins from B. mori and A. pernyi extracted by different methods via the proteomic and immunology as well as the conventional approaches. Great coverage of two cocoon proteomes was accomplished, which demonstrated the outstanding difference in components and abundance. Based on the proteomics analysis, the diagnostic antibodies against two species were prepared and identified the corresponding fibroin successfully in the completed protein mixtures. To our knowledge, the proteomic and immunology procedures with high efficiency, sensitivity and specificity are novel analysis on the silk identification and has great potential in the field of ancient silk detection.
实现丝蛋白的高效鉴定需要高度灵敏的分析技术和有利的提取方法,这对于古代丝绸的研究具有重要意义,特别是对于丝绸起源的争议问题。本文提出了蛋白质组学和 Western blot 方法,用于分析不同方法溶解的家蚕(B. mori)和柞蚕(A. pernyi)丝蛋白。首先,通过光谱法检测二级结构的差异。然后,采用 LC-MS/MS 精确表征丝蛋白肽。LiBr 溶液对家蚕茧具有出色的溶解效果,检测到 87 种蛋白;而铜乙二胺溶液(CED)更适合柞蚕茧,在 A. pernyi-CED 中鉴定出 16 种蛋白。除了丝素和丝胶外,还检测到丰富的丝氨酸、酶、蛋白酶抑制剂、其他功能蛋白和未鉴定的蛋白。基于 LC-MS/MS 数据,制备了两种物种的诊断抗体,并用 Western blot 鉴定了丝素,因为两种溶解方法都很温和,不会破坏蛋白质分子中的抗原表位。由于这些诊断抗体具有良好的特异性和高灵敏度,因此在不同丝绸物种的免疫分析中具有良好的应用前景。意义:本研究通过蛋白质组学和免疫学以及常规方法对不同方法提取的家蚕和柞蚕蛋白的丝鉴定进行了全面分析。完成了两个蚕茧蛋白质组的高覆盖率,表明成分和丰度存在显著差异。基于蛋白质组学分析,制备了针对两种物种的诊断抗体,并成功地在完成的蛋白质混合物中鉴定出相应的丝素。据我们所知,具有高效、高灵敏度和高特异性的蛋白质组学和免疫学程序是对丝鉴定的新分析,在古代丝绸检测领域具有巨大潜力。