| Literature DB >> 27349490 |
Kazuhisa Hirabayashi1, Kenjiro Hanaoka2, Takahiro Egawa1, Chiaki Kobayashi1, Shodai Takahashi1, Toru Komatsu3, Tasuku Ueno1, Takuya Terai1, Yuji Ikegaya1, Tetsuo Nagano4, Yasuteru Urano5.
Abstract
Fluorescence imaging of calcium ions (Ca(2+)) has become an essential technique for investigation of signaling pathways involving Ca(2+) as a second messenger. But, Ca(2+) signaling is involved in many biological phenomena, and therefore simultaneous visualization of Ca(2+) and other biomolecules (multicolor imaging) would be particularly informative. For this purpose, we set out to develop a fluorescent probe for Ca(2+) that would operate in a different color region (red) from that of probes for other molecules, many of which show green fluorescence, as exemplified by green fluorescent protein (GFP). We previously developed a red fluorescent probe for monitoring cytoplasmic Ca(2+) concentration, based on our established red fluorophore, TokyoMagenta (TM), but there remained room for improvement, especially as regards efficiency of introduction into cells. We considered that this issue was probably mainly due to limited water solubility of the probe. So, we designed and synthesized a red-fluorescent probe with improved water solubility. We confirmed that this Ca(2+) red-fluorescent probe showed high cell-membrane permeability with bright fluorescence. It was successfully applied to fluorescence imaging of not only live cells, but also brain slices, and should be practically useful for multicolor imaging studies of biological mechanisms.Entities:
Keywords: Calcium; Fluorescence; Imaging; Small molecule; Spectroscopy
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Year: 2016 PMID: 27349490 DOI: 10.1016/j.ceca.2016.06.002
Source DB: PubMed Journal: Cell Calcium ISSN: 0143-4160 Impact factor: 6.817