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盘基网柄菌趋化过程中肌醇三磷酸和多磷酸的形成。

Inositol tris- and polyphosphate formation during chemotaxis of Dictyostelium.

作者信息

Europe-Finner G N, Gammon B, Wood C A, Newell P C

机构信息

Department of Biochemistry, University of Oxford, UK.

出版信息

J Cell Sci. 1989 Aug;93 ( Pt 4):585-92. doi: 10.1242/jcs.93.4.585.

Abstract

Using the technique of HPLC with Partisil SAX columns, we have found that stimulation of amoebae of Dictyostelium discoideum with the chemoattractant cyclic AMP induces the rapid accumulation of inositol 1,4,5-trisphosphate (Ins(1,4,5)P3), with a peak at 5 s. A smaller HPLC peak (designated P3) that elutes just after the Ins(1,4,5)P3 peak accumulates more slowly to a maximum at 20 s. In control studies, the changes in Ins(1,4,5)P3 were shown not to be due to varying recovery from the cell extracts and a comparison of reverse-phase and Partisil SAX HPLC columns showed similar values for determinations by either method. The involvement of a G-protein in this chemotactic system was confirmed by the finding that accumulation of Ins(1,4,5)P3 was elicited by the addition of GTP gamma S (5'-[gamma-thio]triphosphate) to saponin-permeabilized amoebae. A study of the changes in the lipid-soluble phosphatidyl inositol phosphates demonstrated that cyclic AMP also stimulated a rapid loss of radioactivity from 32P-labelled phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2), which corresponded in its timing to the rise in Ins(1,4,5)P3, indicating that a phosphoinositidase C (phospholipase C) is present that can be stimulated by occupation of the cell surface cyclic AMP receptors.

摘要

运用配备Partisil SAX柱的高效液相色谱法(HPLC)技术,我们发现用趋化剂环磷酸腺苷(cyclic AMP)刺激盘基网柄菌(Dictyostelium discoideum)的变形虫会诱导1,4,5-三磷酸肌醇(Ins(1,4,5)P3)迅速积累,在5秒时达到峰值。在Ins(1,4,5)P3峰之后洗脱的一个较小的HPLC峰(称为P3)积累较慢,在20秒时达到最大值。在对照研究中,Ins(1,4,5)P3的变化并非由于细胞提取物回收率的变化,并且反相HPLC柱和Partisil SAX HPLC柱的比较表明,两种方法测定的值相似。通过向皂角苷通透的变形虫中添加GTPγS(5'-[γ-硫代]三磷酸)可引发Ins(1,4,5)P3积累这一发现,证实了G蛋白参与该趋化系统。对脂溶性磷脂酰肌醇磷酸变化的研究表明,环磷酸腺苷还刺激了32P标记的磷脂酰肌醇4,5-二磷酸(PtdIns(4,5)P2)放射性的快速丧失,其时间与Ins(1,4,5)P3的升高相对应,表明存在一种可被细胞表面环磷酸腺苷受体激活的磷脂酶C。

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