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通过单克隆抗体从鸡胚成纤维细胞中分离出富含原肌球蛋白和富含α-辅肌动蛋白的微丝。

Tropomyosin-enriched and alpha-actinin-enriched microfilaments isolated from chicken embryo fibroblasts by monoclonal antibodies.

作者信息

Lin J J, Matsumura F, Yamashiro-Matsumura S

出版信息

J Cell Biol. 1984 Jan;98(1):116-27. doi: 10.1083/jcb.98.1.116.

Abstract

Antitropomyosin and anti-alpha-actinin monoclonal antibodies have been used to isolate two classes of microfilaments, i.e., tropomyosin-enriched and alpha-actinin-enriched microfilaments, respectively, from cultured chicken embryo fibroblasts. Electron microscopic studies of the isolated tropomyosin-enriched microfilaments showed periodic localization of tropomyosin along the microfilaments, with a 35-nm repeat. On the contrary, the isolated alpha-actinin-enriched microfilaments showed no obvious periodicity. Many individual alpha-actinin-enriched microfilaments with length greater than 1 micron (ranging from 1 to 10 microns) were aggregated by anti-alpha-actinin monoclonal antibodies. Both of the isolated microfilaments had the ability to activate the Mg2+-ATPase activity of skeletal muscle myosin, although different extents of activation were observed. These two classes of microfilaments also differed in their protein composition. Molar ratios of major identifiable proteins in the isolated microfilaments were alpha-actinin(dimer):actin(monomer):tropomyosin(dimer) = less than 0.02:8.06:1.00 for tropomyosin-enriched microfilaments and 0.44:13.91:1.00 for alpha-actinin-enriched microfilaments. By two-dimensional gel analysis of the isolated microfilaments, we have found seven spots which possess typical tropomyosin properties including pI 4.5, immunological cross-reaction, lack of proline and tryptophan, and heat stability. Pulse-chase experiments suggested that the assembly of microfilament-associated proteins, at least for alpha-actinin and tropomyosins, was coordinately regulated by the assembly of actin into microfilaments.

摘要

抗原肌球蛋白和抗α-辅肌动蛋白单克隆抗体已被用于从培养的鸡胚成纤维细胞中分别分离出两类微丝,即富含原肌球蛋白的微丝和富含α-辅肌动蛋白的微丝。对分离出的富含原肌球蛋白的微丝进行电子显微镜研究发现,原肌球蛋白沿微丝呈周期性定位,重复间距为35纳米。相反,分离出的富含α-辅肌动蛋白的微丝没有明显的周期性。许多长度大于1微米(范围为1至10微米)的单个富含α-辅肌动蛋白的微丝被抗α-辅肌动蛋白单克隆抗体聚集。尽管观察到不同程度的激活,但这两类分离出的微丝都有激活骨骼肌肌球蛋白Mg2 + -ATP酶活性的能力。这两类微丝在蛋白质组成上也有所不同。分离出的微丝中主要可识别蛋白质的摩尔比为:对于富含原肌球蛋白的微丝,α-辅肌动蛋白(二聚体):肌动蛋白(单体):原肌球蛋白(二聚体)=小于0.02:8.06:1.00;对于富含α-辅肌动蛋白的微丝,为0.44:13.91:1.00。通过对分离出的微丝进行二维凝胶分析,我们发现了七个具有典型原肌球蛋白特性的斑点,包括pI 4.5、免疫交叉反应、缺乏脯氨酸和色氨酸以及热稳定性。脉冲追踪实验表明,微丝相关蛋白的组装,至少对于α-辅肌动蛋白和原肌球蛋白来说,是由肌动蛋白组装成微丝来协调调节的。

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