Hao Jingfang, Malnoë Alizée
Umeå Plant Science Centre (UPSC), Department of Plant Physiology, Umeå University, 901 87 Umeå, Sweden.
Bio Protoc. 2023 Aug 5;13(15):e4756. doi: 10.21769/BioProtoc.4756.
The chloroplast lumen contains at least 80 proteins whose function and regulation are not yet fully understood. Isolating the chloroplast lumen enables the characterization of the lumenal proteins. The lumen can be isolated in several ways through thylakoid disruption using a Yeda press or sonication, or through thylakoid solubilization using a detergent. Here, we present a simple procedure to isolate thylakoid lumen by sonication using leaves of the plant . The step-by-step procedure is as follows: thylakoids are isolated from chloroplasts, loosely associated thylakoid surface proteins from the stroma are removed, and the lumen fraction is collected in the supernatant following sonication and centrifugation. Compared to other procedures, this method is easy to implement and saves time, plant material, and cost. Lumenal proteins are obtained in high quantity and purity; however, some stromal membrane-associated proteins are released to the lumen fraction, so this method could be further adapted if needed by decreasing sonication power and/or time.
叶绿体腔中至少含有80种蛋白质,其功能和调控机制尚未完全明确。分离叶绿体腔有助于对腔蛋白进行表征。可以通过几种方法分离腔,包括使用耶达压榨机或超声处理使类囊体破裂,或使用去污剂使类囊体溶解。在此,我们介绍一种使用植物叶片通过超声处理分离类囊体腔的简单方法。具体步骤如下:从叶绿体中分离出类囊体,去除来自基质的松散结合在类囊体表面的蛋白质,然后在超声处理和离心后,将腔部分收集在上清液中。与其他方法相比,该方法易于实施,节省时间、植物材料和成本。可获得大量且纯度高的腔蛋白;然而,一些与基质膜相关的蛋白质会释放到腔部分中,因此如果需要,可以通过降低超声处理的功率和/或时间对该方法进行进一步改进。