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从糯米香叶片中提取的蛋白质分析方法的建立。

Method development for analysis of proteins extracted from the leaves of Orthosiphon aristatus.

机构信息

School of Pharmaceutical Sciences, Universiti Sains Malaysia, USM, Penang, Malaysia.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jul 15;879(22):2179-83. doi: 10.1016/j.jchromb.2011.05.041. Epub 2011 Jun 6.

Abstract

Orthosiphon aristatus is a traditionally used medicinal plant. In order to study the proteome of the plant, we have developed a simple plant protein extraction method by direct extraction of protein using a modified 2D-gel compatible tris-sucrose buffer followed by a double TCA-acetone precipitation. This method omitted the use of toxic phenol which is widely used in the studies of plants proteins. Moreover, it shortens the lengthy extraction procedure of phenol extraction and back-extraction method and therefore reduced the extraction time (by 2h) while increased in protein yields (by 50%). Comparison of the 2D-gel images of the two extracts revealed that >60 extra protein spots were detected in the extract of our current method. The method was applied on the leaves of O. aristatus collected from six geographical areas in Malaysia. The correlation coefficient of each replicate gels from the six areas ranged from 0.70 to 0.90 indicating good reproducibility of the method.

摘要

过岗龙是一种传统药用植物。为了研究该植物的蛋白质组,我们开发了一种简单的植物蛋白提取方法,即用改良的 2D 胶兼容的三蔗糖缓冲液直接提取蛋白质,然后进行两次三氯乙酸-丙酮沉淀。该方法省去了广泛用于植物蛋白研究的有毒苯酚的使用。此外,它缩短了苯酚提取和反萃取方法的冗长提取过程,从而减少了提取时间(2 小时),同时增加了蛋白质产量(50%)。两种提取物的 2D 凝胶图像比较显示,我们当前方法的提取物中检测到了 >60 个额外的蛋白质斑点。该方法应用于从马来西亚六个地区采集的过岗龙叶片。来自六个地区的每个重复凝胶的相关系数范围为 0.70 至 0.90,表明该方法具有良好的重现性。

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