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首页> 外文期刊>Journal of cell biology >Study of the mechanism of vanadate inhibition of the dynein cross-bridge cycle in sea urchin sperm flagella
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Study of the mechanism of vanadate inhibition of the dynein cross-bridge cycle in sea urchin sperm flagella

机译:钒酸盐抑制海胆精子鞭毛动力蛋白跨桥循环的机制研究

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The effect of vanadate on the ATP-induced disruption of trypsin-treated axonemes and the ATP-induced straightening of rigor wave preparations of sea urchin sperm was investigated. Addition of ATP to a suspension of trypsin-treated axonemes results in a rapid decrease in turbidity (optical density measured at 350 nm) concomitant with the disruption of the axonemes by sliding between microtubules to form tangles of connected doublet microtubules (Summers and Gibbons, 1971; Sale and Satir, 1977). For axonemes digested to approximately 93 percent of their initial turbidity, 5 {muM} vanadate completely inhibits the ATP-induced decrease in turbidity and the axonemes maintain their structural integrity. However, with axonemes digested to approximately 80 percent of their initial turbidity, vanadate fails to inhibit the ATP-induced decrease in turbidity and the ATP-induced structural disruption of axonemes, even when the vanadate concentration is raised as high as 100 μm. For such axonemes digested to 80 percent of their initial turbidity, the form of ATP-induced structural changes, in the presence of 25 μM vanadate, was observed by dark-field light microscopy and revealed that the axonemes become disrupted into curved, isolated doublet microtubules, small groups of doublet microtubules, and "banana peel" structures in which tubules have peeled back from the axoneme. Addition of 5 μM ATP to rigor wave sperm, which were prepared by abrupt removal of ATP from reactivated sperm, causes straightening of the rigor waves within 1 min, and addition of more than 10 μM ATP causes resumption of flagellar beating. Addition of 40 μM vanadate to the rigor wave sperm does not inhibit straightening of the rigor waves of 2 μM-1 mM ATP, although oscillatory beating is completely inhibited. These results suggest that vanadate inhibits the mechanochemical cycle of dyein at a step subsequent to the MgATP(2-)-induced release of the bridged dynein arms.
机译:研究了钒酸盐对ATP诱导的胰蛋白酶处理的轴突破坏和海藻精子的严格波制剂的ATP矫直的影响。在经过胰蛋白酶处理的轴突悬浮液中添加ATP会导致浊度快速降低(在350 nm处测得的光学密度),同时伴随着轴突的破坏,通过在微管之间滑动形成缠结的双峰微管(Summers和Gibbons,1971年) ; Sale and Satir,1977)。对于被消化至其初始浊度约93%的轴蛋白,5 {μM}钒酸盐完全抑制了ATP引起的浊度降低,并且轴蛋白保持其结构完整性。但是,将轴酮消化至其初始浊度的大约80%时,即使当钒酸盐浓度升高至100μm时,钒酸盐也无法抑制ATP引起的浊度降低和ATP引起的轴突结构破坏。对于这种被消化至其初始浊度为80%的轴索蛋白,在25μM钒酸盐存在的情况下,通过暗场光学显微镜观察到了ATP诱导的结构变化的形式,结果表明轴索蛋白被破坏成弯曲的,分离的双峰微管。 ,一小组的双重态微管和“香蕉皮”结构,其中小管已从轴突中剥离了下来。通过从重新激活的精子中突然去除ATP制备的5μMATP添加到严格的精子中,可在1分钟内使僵直的波直,而添加超过10μM的ATP则可导致鞭毛跳动的恢复。尽管严格抑制了振荡跳动,但向严格波精子中添加40μM钒酸盐不会抑制2μM-1mM ATP严格波的矫直。这些结果表明,钒酸盐在MgATP(2-)诱导的桥接的达因臂释放后的一步抑制染料的机械化学循环。

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