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通过体外酶重折叠试验筛选印楝提取物的微生物抗伴侣活性。

Screening of Neem extracts for microbial anti-chaperone activity by employing in vitro enzyme refolding assay.

作者信息

Patki Jyoti M, Shah Priyanka

机构信息

School of Biotechnology and Bioinformatics, D.Y.Patil University, Sector-15, Plot-50, CBD Belapur, Navi Mumbai, India.

出版信息

3 Biotech. 2017 Oct;7(5):277. doi: 10.1007/s13205-017-0911-6. Epub 2017 Aug 4.

Abstract

Microbial heat shock proteins (Hsps) play an important role in pathogenesis and development of resistance to existing drugs. New compounds that target microbial molecular chaperones have the potential of combating the challenge of anti-microbial resistance. The present study was aimed at assessing the employment of in vitro enzyme refolding assay to detect anti-chaperone activity of Neem () extracts. Protein extracts of thermotolerant cells were used as a source of Hsps or chaperones. Thermotolerance was found to be induced by pre-treating cells at 47 °C before subjecting them to a lethal temperature of 55 °C. This thermotolerance correlated with over-expression of specific proteins and reduced aggregation as evident from the SDS-PAGE profiles. Refolding assays of denatured enzymes exhibited 45% activity regain in presence of cell protein extracts containing chaperones compared to less than 5% regain in BSA negative controls. The chaperone activity was found to be ATP dependent. Addition of Neem extracts to refolding reaction mixtures distinctly reduced the activity regain (20%) in a dose dependent manner (500 and 1000 ppm). The negative influence of plant extract on refolding of the enzyme in the presence of chaperones gives evidence to its anti-chaperone activity. We propose that the employment of in vitro enzyme refolding assays will help not only to analyze the activity of known and putative chaperones but also to screen natural compounds for anti-microbial-Hsp activity.

摘要

微生物热休克蛋白(Hsps)在发病机制及对现有药物的耐药性发展中发挥着重要作用。靶向微生物分子伴侣的新型化合物具有应对抗菌耐药性挑战的潜力。本研究旨在评估利用体外酶重折叠试验检测印楝提取物的抗伴侣活性。耐热细胞的蛋白质提取物用作热休克蛋白或伴侣蛋白的来源。在将细胞置于55℃致死温度之前,先在47℃对其进行预处理,发现可诱导耐热性。从SDS-PAGE图谱明显可见,这种耐热性与特定蛋白质的过表达及聚集减少相关。与BSA阴性对照中不到5%的活性恢复相比,在含有伴侣蛋白的细胞蛋白质提取物存在下,变性酶的重折叠试验显示活性恢复了45%。发现伴侣活性依赖于ATP。在重折叠反应混合物中添加印楝提取物,以剂量依赖方式(500和1000 ppm)显著降低了活性恢复(20%)。植物提取物对伴侣蛋白存在下酶重折叠的负面影响证明了其抗伴侣活性。我们提出,利用体外酶重折叠试验不仅有助于分析已知和推定伴侣蛋白的活性,还能筛选具有抗微生物热休克蛋白活性的天然化合物。

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