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用Ca2+敏感荧光染料indo-1测量酵母细胞中的胞质和液泡Ca2+浓度。

Cytosolic and vacuolar Ca2+ concentrations in yeast cells measured with the Ca2+-sensitive fluorescence dye indo-1.

作者信息

Halachmi D, Eilam Y

机构信息

Department of Bacteriology, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

FEBS Lett. 1989 Oct 9;256(1-2):55-61. doi: 10.1016/0014-5793(89)81717-x.

Abstract

Cells of Saccharomyces cerevisiae were loaded with indo-1, by incubation in a medium of pH 4.5, which contained penta-potassium indo-1. Cells were then washed and resuspended in a buffer of pH 4.0. The emission fluorescence spectra were recorded between 390 and 500 nm (excitation at 355 nm) and the autofluorescent spectra of the matched controls were subtracted. A 19-fold cellular accumulation of indo-1 was achieved. By permeabilization of plasma membranes, leaving the vacuolar membrane intact, it was proved that indo-1 was accumulated in the cytosol. It was also shown that intracellular indo-1 did not leak out of the cells and was not modified by cellular metabolism. Using the emission fluorescence ratio at 410/480 nm, the concentration of a free cytosolic Ca2+ was found to be 346 nM. Vacuolar Ca2+ concentration, calculated from indo-1 fluorescence after lysis of vacuolar and cellular membranes, was found to be 1.3 mM.

摘要

通过在含有五钾吲哚酚 -1的pH 4.5培养基中孵育,将酿酒酵母细胞用吲哚酚 -1加载。然后洗涤细胞并将其重悬于pH 4.0的缓冲液中。在390至500nm之间记录发射荧光光谱(在355nm激发),并减去匹配对照的自发荧光光谱。实现了吲哚酚 -1在细胞内19倍的积累。通过使质膜通透化而使液泡膜保持完整,证明吲哚酚 -1积累在细胞质中。还表明细胞内的吲哚酚 -1不会从细胞中泄漏出来,也不会被细胞代谢修饰。使用410/480nm处的发射荧光比率,发现游离细胞质Ca2+的浓度为346nM。根据液泡膜和细胞膜裂解后的吲哚酚 -1荧光计算,液泡Ca2+浓度为1.3mM。

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