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Molecular characterization of heat shock proteins 90 (HSP83?) and 70 in tropical strains of Bombyx mori

机译:热带家蚕菌株热激蛋白90(HSP83?)和70的分子表征

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摘要

Following the concept of whole organism, we have extracted total protein from the Bombyx mori for the identification and analysis of HSPs. Expression of 90 kDa HSP in first, second and third instars, 84 kDa in fourth instar and 90-, 84-, 62-, 60-, 52- and 33-kDa HSPs in fifth instar larvae of tropical polyvoltine and bivoltine silkworm strains were obvious. Further, we have combined single and 2-DE with MALDI-TOF for analysis of BmHSPs. Ninety kilodalton band excised from 1-DE gel was identified as HSP83 by MALDI-TOF-MS. The immunoblot analysis confirmed the expression of HSP90 in all the instars larvae of B. mori. Heat shock-induced protein spots were excised from 2-DE gels for MALDI-TOF-MS analysis. The Mascot search results are for HSP68, HSC70-1 and HSP70Ba in Pure Mysore, and major HSP70Bbb, HSP68, HSC-3 and HSP83 in NB 4D 2. Multiple sequence alignment explicit the variations in amino acid sequence between Pure Mysore and NB 4D 2. Notably, the PMF of spot 2 matched the coding sequence of B. mori and its gene annotation was determined on chromosome 9. With this novel approach, expression of BmHSP90 was confirmed in all the instars and uncovered isoforms of BmHSP70, which provided unequivocal insight to analyze and understand the biological significance in B. mori.
机译:遵循整个生物体的概念,我们从家蚕中提取了总蛋白,用于鉴定和分析HSP。热带多伏和双伏蚕品系在第一,第二和第三龄幼虫中表达90 kDa HSP,在第四龄幼虫中表达84 kDa,在第五龄幼虫中表达90、84、62、60、52和33 kDa HSP。明显。此外,我们将单和2-DE与MALDI-TOF结合使用以分析BmHSP。从1-DE凝胶切下的九十道尔顿带通过MALDI-TOF-MS鉴定为HSP83。免疫印迹分析证实了HSP90在桑蚕所有幼虫中的表达。从2-DE凝胶上切下热激诱导的蛋白质斑点,以进行MALDI-TOF-MS分析。 Mascot搜索结果针对的是纯迈索尔中的HSP68,HSC70-1和HSP70Ba,以及NB 4D 2中的主要HSP70Bbb,HSP68,HSC-3和HSP83。多序列比对明确了Pure Mysore和NB 4D 2之间的氨基酸序列差异。值得注意的是,斑点2的PMF匹配了桑蚕的编码序列,并在染色体9上确定了其基因注释。通过这种新方法,在所有BmHSP70的幼虫和未发现的亚型中都证实了BmHSP90的表达,这提供了明确的见解分析和了解家蚕的生物学意义。

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