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烟草叶肉原生质体表面糖基磷脂酰肌醇锚定蛋白的检测

Detection of glycosyl-phosphatidylinositol-anchored proteins on the surface of Nicotiana tabacum protoplasts.

作者信息

Takos A M, Dry I B, Soole K L

机构信息

Centre for Plant Membrane Biology, School of Biological Sciences, The Flinders University of South Australia, Adelaide.

出版信息

FEBS Lett. 1997 Mar 17;405(1):1-4. doi: 10.1016/s0014-5793(97)00064-1.

Abstract

Glycosyl-phosphatidylinositol (GPI)-anchored plasma membrane proteins have been found to be widespread in eukaryotes and protozoa but have not been reported in higher terrestrial plants. A sensitive biotin-based assay has been used to detect the presence of GPI-anchored proteins on the outer surface of cultured Nicotiana tabacum cells. Six proteins with molecular weights of 92, 84, 60.5, 54.5, 39.5 and 37 kDa were found to move from a Triton X-114 detergent-rich phase to an aqueous phase following incubation with phosphatidylinositol-specific phospholipase C (PtdIns-PLC). The behaviour of these proteins is consistent with the presence of a GPI-anchor. Seven GPI-anchored proteins were also detected on the surface of tobacco leaf protoplasts with molecular weights of 67.5, 62, 39, 33.5, 27, 23 and 15.6 kDa. These data demonstrate the presence of multiple GPI-anchored proteins on the plasma membrane of higher plant cells.

摘要

糖基磷脂酰肌醇(GPI)锚定的质膜蛋白已被发现广泛存在于真核生物和原生动物中,但尚未在高等陆生植物中报道。一种基于生物素的灵敏检测方法已被用于检测培养的烟草细胞外表面上GPI锚定蛋白的存在。发现分子量分别为92、84、60.5、54.5、39.5和37 kDa的六种蛋白质在与磷脂酰肌醇特异性磷脂酶C(PtdIns-PLC)孵育后,从富含Triton X-114洗涤剂的相转移到水相。这些蛋白质的行为与存在GPI锚定一致。在烟草叶原生质体表面还检测到七种GPI锚定蛋白,分子量分别为67.5、62、39、33.5、27、23和15.6 kDa。这些数据证明高等植物细胞质膜上存在多种GPI锚定蛋白。

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