Department of Laboratory Medicine, Center for Diagnostic Oncology, Research Institute and Hospital, National Cancer Center, Goyang-si, Republic of Korea.
PLoS One. 2013 Sep 5;8(9):e73408. doi: 10.1371/journal.pone.0073408. eCollection 2013.
Nanoparticles (NPs) are attractive materials owing to their physical and electrochemical properties, which make them extremely useful in diagnostic applications. Photon upconversion is the phenomenon where high-energy photons are emitted upon excitation of low-energy photons. Nucleic acids detection based on upconversion nanoparticles (UCNPs), which display a high signal-to-noise ratio and no photobleaching, has been widely applied. We evaluated whether UCNPs can improve polymerase chain reaction (PCR) specificity and affect PCR amplification. The effects of UCNPs with a diameter size of 40, 70, and 250 nm were evaluated using 3 PCR kits (AccuPower PCR PreMix, AmpliTaq Gold 360 Master Mix, and HotStarTaq Plus Master Mix) and 3 real-time PCR kits (AccuPower GreenStar qPCR PreMix, SYBR Green PCR Master Mix, and QuantiTect SYBR Green PCR Kit). Quantum dots were used for comparison with the UCNPs. In the presence of an appropriate concentration of UCNPs, PCR specificity was optimized. UCNPs of 40-nm size improved PCR specificity more effectively than did UCNPs sized 70 or 250 nm. As the size and concentrations of the UCNPs were increased, PCR amplification was more severely inhibited. At lower annealing temperatures (25°C-45°C), addition of the 40 nm UCNP (1 µg/µL) to the PCR reagent produced specific PCR products without nonspecific sequence amplification. Therefore, UCNPs of different sizes, with different DNA polymerases used in the commercial kits, showed different inhibitory effects on PCR amplification. These results demonstrate that optimization of UCNPs, added to reaction mixtures at appropriate concentrations, can improve PCR specificity. However, the mechanism underlining UCNPs effect on PCR remains unclear and will require further investigation.
纳米粒子(NPs)因其物理和电化学性质而成为极具吸引力的材料,使其在诊断应用中非常有用。上转换是指在激发低能光子时发射高能光子的现象。基于上转换纳米粒子(UCNPs)的核酸检测具有高信噪比和无荧光漂白的特点,因此得到了广泛的应用。我们评估了 UCNPs 是否可以提高聚合酶链反应(PCR)的特异性并影响 PCR 扩增。使用 3 种 PCR 试剂盒(AccuPower PCR PreMix、AmpliTaq Gold 360 Master Mix 和 HotStarTaq Plus Master Mix)和 3 种实时 PCR 试剂盒(AccuPower GreenStar qPCR PreMix、SYBR Green PCR Master Mix 和 QuantiTect SYBR Green PCR Kit)评估了直径分别为 40、70 和 250nm 的 UCNPs 的效果。使用量子点与 UCNPs 进行比较。在适当浓度的 UCNPs 存在下,优化了 PCR 的特异性。与尺寸为 70 或 250nm 的 UCNPs 相比,尺寸为 40nm 的 UCNPs 更有效地提高了 PCR 的特异性。随着 UCNPs 的尺寸和浓度的增加,PCR 扩增受到的抑制更为严重。在较低的退火温度(25°C-45°C)下,将 40nm UCNP(1µg/µL)添加到 PCR 试剂中可产生特异性 PCR 产物,而无非特异性序列扩增。因此,不同尺寸的 UCNPs 与商业试剂盒中使用的不同 DNA 聚合酶对 PCR 扩增表现出不同的抑制作用。这些结果表明,优化添加到反应混合物中的 UCNPs,使其浓度适当,可以提高 PCR 的特异性。然而,UCNPs 对 PCR 影响的机制尚不清楚,需要进一步研究。