Jemilohun P F
Department of Biology, Jackson State University, MS 39217, USA.
Parasitol Res. 1998 Oct;84(10):800-5. doi: 10.1007/s004360050491.
As a first step in the biochemical and biomedical analyses of flagella from Trichomonas vaginalis the flagella were isolated, purified, and analyzed. The flagella were detached by mechanical shearing and a crude flagellar preparation was obtained by low-speed differential centrifugation. The crude flagellar preparation was subjected to further purification by discontinuous sucrose density-gradient centrifugation. Electron micrographs (EM) of the purified flagella showed the typical 9 + 2 axonemal arrangement. The structural integrity and the flagellar membrane were not destroyed by the deflagellation method or the purification scheme employed. The flagellar preparations were resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The purified preparation contained many flagellar enriched proteins ranging from 20 to 120 kDa. Three major proteins of 65 kDa and a doublet of about 50-58 kDa were observed. The protein patterns and EM appearance of the fractions were highly reproducible.
作为对阴道毛滴虫鞭毛进行生化和生物医学分析的第一步,对鞭毛进行了分离、纯化和分析。通过机械剪切使鞭毛脱离,经低速差速离心获得粗制鞭毛制剂。粗制鞭毛制剂通过不连续蔗糖密度梯度离心进一步纯化。纯化鞭毛的电子显微镜照片显示出典型的9 + 2轴丝排列。去鞭毛方法或所采用的纯化方案均未破坏结构完整性和鞭毛膜。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳对鞭毛制剂进行分析。纯化制剂包含许多分子量在20至120 kDa之间的富含鞭毛的蛋白质。观察到三种65 kDa的主要蛋白质和一组约50 - 58 kDa的双条带蛋白质。各组分的蛋白质图谱和电子显微镜外观具有高度可重复性。