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由肌动蛋白结合蛋白和肌动蛋白制备的凝胶的精细结构:与盘基网柄菌变形虫细胞的胞质提取物和皮质细胞质的比较。

Fine structure of gels prepared from an actin-binding protein and actin: comparison to cytoplasmic extracts and cortical cytoplasm in amoeboid cells of cortical cytoplasm in amoeboid cells of Dictyostelium discoideum.

作者信息

Wolosewick J J, Condeelis J

出版信息

J Cell Biochem. 1986;30(3):227-43. doi: 10.1002/jcb.240300305.

Abstract

We have identified the three-dimensional ultrastructure of actin gels that are formed in well-characterized cell extracts and mixtures of purified actin and the 120K actin-binding protein and compared these to the ultrastructure of the cytoplasmic matrix in regions of nonextracted Dictyostelium amoebae that are rich in actin and 120K. This ultrastructural characterization was achieved by using critical-point-dried whole-mount preparations. All three preparations--gelled extracts, purified proteins, and cortical cytoplasm--are composed of filament networks. The basic morphological feature of these networks is the presence of contacts between convergent filaments resulting in "T" or "X" shaped contacts. The finding that actin-containing gels are composed of filament networks, where the primary interaction occurs between convergent filaments, reconciles the known requirement of F actin for gelation with the amorphous appearance of these gels in thin sections. Increasing the molar ratio of 120K dimer to actin monomer increases the number of contacts between filaments per unit volume and decreases the lengths of filaments between contacts. This indicates that 120K stabilizes interactions between filaments and is consistent with biochemical evidence that 120K crosslinks actin filaments. The cortical network in situ resembles more closely networks formed in 120K-rich extracts than networks assembled in mixtures of purified 120K and actin. The heterogeneity of filament diameters and variation of network density are properties shared by extracts and the cytomatrix in situ while networks found in purified 120K-actin gels have filament diameters and densities that are more uniform. These differences are certainly due to the more complex composition of cell extracts and cortical cytoplasm as compared to that of purified 120K-actin gels.

摘要

我们已经确定了在特征明确的细胞提取物以及纯化肌动蛋白与120K肌动蛋白结合蛋白的混合物中形成的肌动蛋白凝胶的三维超微结构,并将其与未提取的富含肌动蛋白和120K的盘基网柄菌变形虫区域中的细胞质基质的超微结构进行了比较。这种超微结构表征是通过使用临界点干燥的整装制剂实现的。所有三种制剂——凝胶化提取物、纯化蛋白和皮质细胞质——均由丝状网络组成。这些网络的基本形态特征是汇聚的细丝之间存在接触,形成“T”形或“X”形接触。含肌动蛋白的凝胶由丝状网络组成,其中主要相互作用发生在汇聚的细丝之间,这一发现使F肌动蛋白凝胶化的已知要求与这些凝胶在薄切片中的无定形外观相协调。增加120K二聚体与肌动蛋白单体的摩尔比会增加单位体积内细丝之间的接触数量,并减少接触之间细丝的长度。这表明120K稳定了细丝之间的相互作用,并且与120K交联肌动蛋白细丝的生化证据一致。原位皮质网络与富含120K的提取物中形成的网络比与纯化的120K和肌动蛋白混合物中组装的网络更相似。细丝直径的异质性和网络密度的变化是提取物和原位细胞基质共有的特性,而在纯化的120K-肌动蛋白凝胶中发现的网络具有更均匀的细丝直径和密度。这些差异肯定是由于与纯化的120K-肌动蛋白凝胶相比,细胞提取物和皮质细胞质的组成更为复杂。

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