Suppr超能文献

一种改进的细胞质动力蛋白纯化方法。

An improved purification method for cytoplasmic dynein.

作者信息

Pratt M M, Hisanaga S, Begg D A

出版信息

J Cell Biochem. 1984;26(1):19-33. doi: 10.1002/jcb.240260103.

Abstract

An improved method has been devised for the purification of cytoplasmic dynein from sea urchin eggs (Strongylocentrotus droebachiensis and S purpuratus). This protocol introduces three changes over a previously published procedure (Hisanaga and Sakai: J Biochem 93:87, 1983)--the substitution of diethylaminoethyl (DEAE)-cellulose for hydroxylapatite chromatography, the elimination of sucrose density gradient centrifugation, and the use of phosphocellulose chromatography. These changes reduce the time and increase the efficiency of the purification procedure. The purified egg cytoplasmic dynein has enzymatic properties in common with axonemal dynein, including ionic specificity (Ca++ATPase/Mg++ ATPase = 0.8) and inhibition by sodium vanadate and erythro-9-2,3-hydroxynonyl adenine (EHNA). As assayed by silver staining of polyacrylamide gels, the cytoplasmic dynein is composed of two high molecular weight polypeptides (greater than 300 kilodaltons) that comigrate with flagellar dynein heavy chains, and lesser amounts of three lower molecular weight bands. None of these polypeptides appears to contain bound carbohydrate. The purification procedure can be modified slightly to allow the preparation of cytoplasmic dynein in only 2 days from as little as 3-5 ml of packed eggs, a 20-fold reduction over the previous method. This more rapid and efficient method will facilitate the investigation of cytoplasmic dynein in other systems where starting material is limited, including tissue culture cells and nerve axoplasm.

摘要

已设计出一种改进方法,用于从海胆卵(强壮海胆和紫海胆)中纯化细胞质动力蛋白。该方案相对于先前发表的方法(久永与酒井:《生物化学杂志》93:87,1983)有三处改动——用二乙氨基乙基(DEAE)纤维素替代羟基磷灰石色谱法、取消蔗糖密度梯度离心法以及采用磷酸纤维素色谱法。这些改动减少了时间并提高了纯化过程的效率。纯化后的卵细胞质动力蛋白具有与轴丝动力蛋白相同的酶学特性,包括离子特异性(Ca++ATP酶/Mg++ATP酶 = 0.8)以及对钒酸钠和赤藓红 - 9 - 2,3 - 羟基壬基腺嘌呤(EHNA)的抑制作用。通过聚丙烯酰胺凝胶银染分析,细胞质动力蛋白由两条高分子量多肽(大于300千道尔顿)组成,它们与鞭毛动力蛋白重链迁移率相同,还有少量三条低分子量条带。这些多肽似乎都不含有结合型碳水化合物。纯化步骤可稍作修改,仅用3 - 5毫升压实的卵在短短2天内就能制备细胞质动力蛋白,比之前的方法减少了20倍。这种更快且更高效的方法将有助于在起始材料有限的其他系统中研究细胞质动力蛋白,包括组织培养细胞和神经轴浆。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验