Phospholipid-Modified Upconversion Nanoprobe for Ratiometric Fluorescence Detection and Imaging of Phospholipase D in Cell Lysate and in Living Cells

• Published in: Analytical chemistry (Washington) 2014-07, Vol.86 (14), p.7119-7127
• Main Authors: Cen, Yao, Wu, Yan-Mei, Kong, Xiang-Juan, Wu, Shuang, Yu, Ru-Qin, Chu, Xia
• Format: Article
• Language: English
• Subjects: Cell Line - enzymology; Cell Line, Tumor - enzymology; Cellular biology; Emission; Enzymes; Fluorescence; Fluorescence in situ hybridization; Fluorescence Resonance Energy Transfer - methods; Gene expression; Humans; Hydrolysis; Lipids; Molecular Imaging - instrumentation; Molecular Imaging - methods; Nanoparticles - chemistry; Nanostructure; Phospholipase D - analysis; Phospholipids; Phospholipids - chemistry; Polyethylene Glycols - chemistry; Rhodamine; Rhodamines - chemistry; Self assembly; Solutions; Surface chemistry; Upconversion; Ytterbium - chemistry; Yttrium - chemistry
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac5016694

Phospholipase D (PLD) is a critical component of intracellular signal transduction and has been implicated in many important biological processes. It has been observed that there are abnormalities in PLD expression in many human cancers, and PLD is thus recognized as a potential diagnostic biomarker as well as a target for drug discovery. We report for the first time a phospholipid-modified nanoprobe for ratiometric upconversion fluorescence (UCF) sensing and bioimaging of PLD activity. The nanoprobe can be synthesized by a facile one-step self-assembly of a phospholipid monolayer composed of poly­(ethylene glycol) (PEG)­ylated phospholipid and rhodamine B-labeled phospholipid on the surface of upconversion nanoparticles (UCNPs) NaYF4: 20%Yb, 2%Er. The fluorescence resonance energy transfer (FRET) process from the UCF emission at 540 nm of the UCNPs to the absorbance of the rhodamine B occurs in the nanoprobe. The PLD-mediated hydrolysis of the phosphodiester bond makes rhodamine B apart from the UCNP surface, leading to the inhibition of FRET. Using the unaffected UCF emission at 655 nm as an internal standard, the nanoprobe can be used for ratiometric UCF detection of PLD activity with high sensitivity and selectivity. The PLD activity in cell lysates is also determined by the nanoprobe, confirming that PLD activity in a breast cancer cell is at least 7-fold higher than in normal cell. Moreover, the nanoprobe has been successfully applied to monitoring PLD activity in living cells by UCF bioimaging. The results reveal that the nanoprobe provides a simple, sensitive, and robust platform for point-of-care diagnostics and drug screening in biomedical applications.