Corporate Research and Development Center, Olympus Corporation, Kuboyama 2-3, Hachioji, Tokyo 192-8512, Japan.
Luminescence. 2013 Jul-Aug;28(4):582-91. doi: 10.1002/bio.2497. Epub 2013 Mar 6.
We isolated and characterized a green fluorescent protein (GFP) from the sea cactus Cavernularia obesa. This GFP exists as a dimer and has absorption maxima at 388 and 498 nm. Excitation at 388 nm leads to blue fluorescence (456 nm maximum) at pH 5 and below, and green fluorescence (507 nm maximum) at pH 7 and above, and the GFP is remarkably stable at pH 4. Excitation at 498 nm leads to green fluorescence (507 nm maximum) from pH 5 to pH 9. We introduced five amino acid substitutions so that this GFP formed monomers rather than dimers and then used this monomeric form to visualize intracellular pH change during the phagocytosis of living cells by use of fluorescence microscopy. The intracellular pH change is visualized by use of a simple long-pass emission filter with single-wavelength excitation, which is technically easier to use than dual-emission fluorescent proteins that require dual-wavelength excitation.
我们从海仙人掌 Cavernularia obesa 中分离并鉴定了一种绿色荧光蛋白 (GFP)。这种 GFP 以二聚体的形式存在,在 pH 值为 5 及以下时,其吸收最大值在 388nm 和 498nm 处;在 pH 值为 7 及以上时,其激发波长为 388nm,发出的荧光为蓝色(最大发射波长为 456nm);在 pH 值为 4 时,GFP 具有显著的稳定性。当激发波长为 498nm 时,GFP 在 pH 值为 5 到 9 之间发出绿色荧光(最大发射波长为 507nm)。我们引入了五个氨基酸取代,使这种 GFP 形成单体而不是二聚体,然后使用这种单体形式通过荧光显微镜可视化活细胞吞噬过程中的细胞内 pH 值变化。通过使用具有单波长激发的简单长通发射滤光片来可视化细胞内 pH 值变化,这种方法在技术上比需要双波长激发的双发射荧光蛋白更容易使用。