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Actin-Dynamics in Plant Cells: The Function of Actin Perturbing Substances Jasplakinolide Chondramides Phalloidin Cytochalasins and Latrunculins

机译:植物细胞中的肌动蛋白动力学:肌动蛋白摄动物质Jasplakinolide软骨素鬼笔环肽细胞松弛素和Latrunculins的功能

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摘要

This chapter will give an overview of the most common F-actin perturbing substances, that are used to study actin dynamics in living plant cells in studies on morphogenesis, motility, organelle movement or when apoptosis has to be induced. These substances can be divided into two major subclasses – F-actin stabilizing and polymerizing substances like jasplakinolide, chondramides and F-actin severing compounds like chytochalasins and latrunculins. Jasplakinolide was originally isolated form a marine sponge, and can now be synthesized and has become commercially available, which is responsible for its wide distribution as membrane permeable F-actin stabilizing and polymerizing agent, which may even have anti-cancer activities. Cytochalasins, derived from fungi show an F-actin severing function and many derivatives are commercially available (A, B, C, D, E, H, J), also making it a widely used compound for F-actin disruption. The same can be stated for latrunculins (A, B), derived from red sea sponges, however the mode of action is different by binding to G-actin and inhibiting incorporation into the filament. In the case of swinholide a stable complex with actin dimers is formed resulting also in severing of F-actin.For influencing F-actin dynamics in plant cells only membrane permeable drugs are useful in a broad range. We however introduce also the phallotoxins and synthetic derivatives, as they are widely used to visualize F-actin in fixed cells. A particular uptake mechanism has been shown for hepatocytes, but has also been described in siphonal giant algae. In the present chapter the focus is set on F-actin dynamics in plant cells where alterations in cytoplasmic streaming can be particularly well studied; however methods by fluorescence applications including phalloidin- and antibody staining as well as immunofluorescence-localization of the inhibitor drugs are given.
机译:本章将概述最常见的F-肌动蛋白扰动物质,这些物质可用于研究活体植物细胞的肌动蛋白动力学,以研究形态发生,运动性,细胞器运动或何时需要诱导凋亡。这些物质可以分为两个主要的子类-F-肌动蛋白稳定和聚合物质,如jasplakinolide,软骨素和F-肌动蛋白切断化合物,如糜蛋白酶和拉特朗库林。 Jasplakinolide最初是从海洋海绵中分离出来的,现在可以合成并已商业化,这是其广泛用作膜渗透性F-肌动蛋白稳定剂和聚合剂的原因,甚至具有抗癌活性。衍生自真菌的细胞松弛素显示F-肌动蛋白切断功能,许多衍生物可商购(A,B,C,D,E,H,J),也使其广泛用于破坏F-肌动蛋白。源自红海海绵的扁桃体蛋白(A,B)也可以说相同,但是其作用方式因与G-肌动蛋白结合并抑制其掺入丝而有所不同。在swinholide的情况下,会形成具有肌动蛋白二聚体的稳定复合物,从而导致F-肌动蛋白的切断。为了影响植物细胞中F-肌动蛋白的动力学,只有膜通透性药物才能广泛使用。但是,我们还介绍了鬼笔毒素和合成衍生物,因为它们被广泛用于可视化固定细胞中的F-肌动蛋白。肝细胞已显示出特定的摄取机制,但虹吸巨藻也已有描述。在本章中,重点放在植物细胞中的F-肌动蛋白动力学上,其中可以特别研究细胞质流的变化。然而,给出了通过荧光应用的方法,包括鬼笔环肽和抗体染色以及抑制剂药物的免疫荧光定位。

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