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激素占据的表皮生长因子受体在质膜制剂上的微聚集。

Microaggregation of hormone-occupied epidermal growth factor receptors on plasma membrane preparations.

作者信息

Zidovetzki R, Yarden Y, Schlessinger J, Jovin T M

出版信息

EMBO J. 1986 Feb;5(2):247-50. doi: 10.1002/j.1460-2075.1986.tb04205.x.

Abstract

The rotational diffusion of the complexes of epidermal growth factor (EGF) with its specific receptor on plasma membrane vesicles prepared from human epidermoid carcinoma A431 cells was studied using the time-resolved polarization of phosphorescence of erythrosin-labeled hormone. The measured rotational correlation times of 16-20 microseconds at 4 degrees C are consistent with monomeric freely diffusing EGF receptor. Upon increasing the temperature to 37 degrees C, the rate of rotational diffusion slows down as evidenced by an increase in the correlation time to 75 microseconds. This finding suggests that small clusters of the occupied EGF receptor (microaggregation) form at the higher temperature, a property we have reported previously for occupied receptors on living A431 cells. Subsequent cooling of the membranes leads to a partial reversal of the microaggregation. We conclude that clustering of occupied EGF receptors can proceed at 37 degrees C in the absence of metabolic energy and external interactions, e.g. with components of the cytoskeleton, and thus reflects inherent properties of the receptor protein in its natural environment. A lag phase in the time course of microaggregation observed with the isolated membrane preparations may reflect cooperativity in the process of receptor association.

摘要

利用赤藓红标记激素磷光的时间分辨极化,研究了表皮生长因子(EGF)与其在源自人表皮样癌A431细胞的质膜囊泡上的特异性受体形成的复合物的旋转扩散。在4℃下测得的16 - 20微秒的旋转相关时间与单体自由扩散的EGF受体一致。将温度升至37℃时,旋转扩散速率减慢,相关时间增加至75微秒就证明了这一点。这一发现表明,在较高温度下会形成被占据的EGF受体小簇(微聚集),这是我们之前报道过的活A431细胞上被占据受体的一个特性。随后对膜进行冷却会导致微聚集部分逆转。我们得出结论,在不存在代谢能量和外部相互作用(例如与细胞骨架成分的相互作用)的情况下,被占据的EGF受体的聚集可以在37℃下进行,因此反映了受体蛋白在其天然环境中的固有特性。在分离的膜制剂中观察到的微聚集时间进程中的延迟阶段可能反映了受体缔合过程中的协同作用。

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本文引用的文献

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Regulation of cell proliferation by epidermal growth factor.表皮生长因子对细胞增殖的调节
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