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三磷酸腺苷(ATP)抑制通透化肥大细胞中胞吐作用的起始。

ATP inhibits onset of exocytosis in permeabilised mast cells.

作者信息

Tatham P E, Gomperts B D

机构信息

Department of Experimental Pathology, University College London, UK.

出版信息

Biosci Rep. 1989 Feb;9(1):99-109. doi: 10.1007/BF01117516.

Abstract

ATP is not required for exocytosis from permeabilised mast cells, and therefore there is no direct role for protein phosphorylation in the late stages of the activation pathway. We have measured the time-course of exocytosis from permeabilised cells triggered to release hexosaminidase following addition of Ca2+ to cells equilibrated for 2 min with GTP-gamma-S. If ATP is included at the time of permeabilization, then exocytosis commences after a delay, the duration of which depends on the square root of the product [Ca2+][GTP-gamma-S], and which may extend to beyond 3 min. When ATP is excluded then the maximal rate of exocytosis is established within 3 secs of completing the effector combination. These results suggest that the achievement of a new steady-state, induced by Ca2+ and GTP-gamma-S, and required for exocytosis is inhibited by ATP. From this we conclude that dephosphorylation of an unknown regulator protein may comprise a step in the exocytotic pathway.

摘要

通透化肥大细胞的胞吐作用不需要ATP,因此在激活途径的后期蛋白质磷酸化没有直接作用。我们测量了在加入Ca2+后触发通透化细胞释放己糖胺酶的胞吐作用的时间进程,这些细胞已用GTP-γ-S平衡2分钟。如果在通透化时加入ATP,那么胞吐作用会延迟开始,延迟的持续时间取决于[Ca2+][GTP-γ-S]乘积的平方根,并且可能会延长到3分钟以上。当排除ATP时,胞吐作用的最大速率在完成效应物组合后的3秒内建立。这些结果表明,由Ca2+和GTP-γ-S诱导的、胞吐作用所需的新稳态的实现受到ATP的抑制。由此我们得出结论,一种未知调节蛋白的去磷酸化可能是胞吐途径中的一个步骤。

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