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Effects of Upconversion Nanoparticles on Polymerase Chain Reaction

机译:上转换纳米粒子对聚合酶链反应的影响

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摘要

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.
机译:纳米颗粒(NPs)由于其物理和电化学特性而成为有吸引力的材料,这使其在诊断应用中极为有用。光子上转换是在激发低能光子时发出高能光子的现象。基于上转换纳米粒子(UCNP)的核酸检测具有高信噪比且无光漂白,已得到广泛应用。我们评估了UCNP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)评估了直径分别为40、70和250 nm的UCNP的效果PreMix,SYBR Green PCR Master Mix和QuantiTect SYBR Green PCR Kit)。量子点用于与UCNP进行比较。在适当浓度的UCNPs存在下,优化了PCR特异性。 40 nm的UCNP比70或250 nm的UCNP更有效地提高了PCR特异性。随着UCNPs大小和浓度的增加,PCR扩增受到更严重的抑制。在较低的退火温度(25°C–45°C)下,向PCR试剂中添加40 nm UCNP(1 µg / µL)可产生特异性PCR产物,而无需非特异性序列扩增。因此,在商业试剂盒中使用不同大小的UCNP和不同的DNA聚合酶,对PCR扩增表现出不同的抑制作用。这些结果表明,以适当的浓度添加到反应混合物中的UCNP的优化可以提高PCR特异性。但是,UCNPs对PCR的影响机制尚不清楚,需要进一步研究。

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