Chen Tzu-Ho, Zhang Shuwei, Jaishi Meghnath, Adhikari Rashmi, Bi Jianheng, Fang Mingxi, Xia Shuai, Zhang Yibin, Luck Rudy L, Pati Ranjit, Lee Hsien-Ming, Luo Fen-Tair, Tiwari Ashutosh, Liu Haiying
Institute of Chemistry, Academia Sinica, Taipei, Taiwan 11529, Republic of China.
Department of Chemistry, National Taiwan University, No. 1 Roosevelt Road Section 4, Taipei 10617, Taiwan, Republic of China.
ACS Appl Bio Mater. 2018 Sep 17;1(3):549-560. doi: 10.1021/acsabm.8b00020. Epub 2018 Aug 2.
Two near-infrared luminescent probes with Stokes-shift and single-photon anti-Stokes-shift fluorescence properties for sensitive determination of pH variance in lysosomes have been synthesized. A morpholine residue in probe which serves as a targeting group for lysosomes in viable cells was attached to the fluorophores via a spirolactam moiety while a mannose residue was ligated to probe resulting in increased biocompatibility and solubility in water. Probes and contain closed spirolactam moieties, and show no Stokes-shift or anti-Stokes-shift fluorescence under neutral or alkali conditions. However, the probes incrementally react to pH variance from 7.22 to 2.76 with measurable increases in both Stokes-shift and anti-Stokes-shift fluorescence at 699 nm and 693 nm under 645 nm and 800 nm excitation, respectively. This acid-activated fluorescence is produced by the breaking of the probe spirolactam moiety, which greatly increased overall π-conjugation in the probes. These probes possess upconversion near-infrared fluorescence imaging advantages including minimum cellular photo-damage, tissue penetration, and minimum biological fluorescence background. They display excellent photostability with low dye photobleaching and show good biocompatibility. They are selective and capable of detecting pH variances in lysosomes at excitation with two different wavelengths, i.e., 645 and 800 nm.
已合成了两种具有斯托克斯位移和单光子反斯托克斯位移荧光特性的近红外发光探针,用于灵敏测定溶酶体中的pH变化。探针中的吗啉残基作为活细胞中溶酶体的靶向基团,通过螺内酰胺部分连接到荧光团上,而甘露糖残基连接到探针上,从而提高了生物相容性和在水中的溶解度。探针和含有封闭的螺内酰胺部分,在中性或碱性条件下不显示斯托克斯位移或反斯托克斯位移荧光。然而,在645 nm和800 nm激发下,探针分别在699 nm和693 nm处对pH从7.22到2.76的变化逐渐产生反应,斯托克斯位移和反斯托克斯位移荧光均有可测量的增加。这种酸激活荧光是由探针螺内酰胺部分的断裂产生的,这大大增加了探针中的整体π共轭。这些探针具有上转换近红外荧光成像优势,包括最小的细胞光损伤、组织穿透性和最小的生物荧光背景。它们表现出优异的光稳定性,染料光漂白低,并显示出良好的生物相容性。它们具有选择性,能够在645和800 nm这两种不同波长激发下检测溶酶体中的pH变化。