包络线(雷达)
质子
天体生物学
材料科学
核物理学
环境科学
化学
物理
工程类
航空航天工程
雷达
作者
Raul Martı́nez-Zaguilán,Souad R. Sennoune
出处
期刊:Methods in molecular biology
日期:2020-01-01
卷期号:: 47-63
被引量:1
标识
DOI:10.1007/978-1-0716-0763-3_5
摘要
The existence of nuclear pore complexes in the nuclear envelope has led to the assumption that ions move freely from the cytosol into the nucleus, and that the molecular mechanisms at the plasma membrane that regulate cytosolic pH also regulate nuclear pH. Furthermore, studies to measure pH in the nucleus have produced contradictory results, since it has been found that the nuclear pH is either similar to the cytosol or more alkaline than the cytosol. However, most studies of nuclear pH have lacked the rigor needed to understand pH regulation in the nucleus. A major problem has been the lack of in situ titrations in the nucleus and cytosol, since the intracellular environment is different in the cytosol and nucleus and the behavior of fluorescent pH probes is different in these environments. Here we present a method that uses the fluorescence of SNARF-1 that labels both cytosol and nucleus. Using ratio imaging microscopy, regions of interest corresponding to the nucleus and cytosol to perform steady-state pH measurements followed by in situ titrations, to correctly assign pH in those cellular domains.
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