Ratiometric fluorescent pH nanoprobes based on in situ assembling of fluorescence resonance energy transfer between fluorescent proteins

被引:4
|
作者
Yu, Haijun [1 ]
Chen, Chao [1 ]
Cao, Xiaodan [1 ]
Liu, Yueling [1 ]
Zhou, Shengmin [1 ]
Wang, Ping [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Sch Biotechnol, Biomed Nanotechnol Ctr, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[2] Univ Minnesota, Dept Bioprod & Biosyst Engn, St Paul, MN 55108 USA
基金
中国国家自然科学基金;
关键词
pH probes; FRET; In situ-assembling; Mesoporous silica nanoparticle; Fluorescent proteins; LIVING CELLS; INTRACELLULAR PH; SINGLE FLUOROPHORE; MESOPOROUS SILICA; QUANTUM DOTS; CANCER-CELLS; BROAD-RANGE; SENSORS; PROBE; ADSORPTION;
D O I
10.1007/s00216-017-0453-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
pH-dependent protein adsorption on mesoporous silica nanoparticle (MSN) was examined as a unique means for pH monitoring. Assuming that the degree of protein adsorption determines the distance separating protein molecules, we examined the feasibility of nanoscale pH probes based on fluorescence resonance energy transfer (FRET) between two fluorescent proteins (mTurquoise2 and mNeonGreen, as donor and acceptor, respectively). Since protein adsorption on MSN is pH-sensitive, both fluorescent proteins were modified to make their isoelectric points (pIs) identical, thus achieving comparable adsorption between the proteins and enhancing FRET signals. The adsorption behaviors of such modified fluorescent proteins were examined along with ratiometric FRET signal generation. Results demonstrated that the pH probes could be manipulated to show feasible sensitivity and selectivity for pH changes in hosting solutions, with a good linearity observed in the pH range of 5.5-8.0. In a demonstration test, the pH probes were successfully applied to monitor progress of enzymatic reactions. Such an "in situ-assembling" pH sensor demonstrates a promising strategy in developing nanoscale fluorescent protein probes.
引用
收藏
页码:5073 / 5080
页数:8
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