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Kelvin probe force microscopy of DNA-capped nanoparticles for single-nucleotide polymorphism detection

机译:开尔文探针DNA-capped力显微镜纳米粒子的单核苷酸多态性检测

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Kelvin probe force microscopy (KPFM) is a robust toolkit for profiling the surface potential (SP) of biomolecular interactions between DNAs and/or proteins at the single molecule level. However, it has often suffered from background noise and low throughput due to instrumental or environmental constraints, which is regarded as limiting KPFM applications for detection of minute changes in the molecular structures such as single-nucleotide polymorphism (SNP). Here, we show KPFM imaging of DNA-capped nanoparticles (DCNP) that enables SNP detection of the BRCA1 gene owing to sterically well-adjusted DNA-DNA interactions that take place within the confined spaces of DCNP. The average SP values of DCNP interacting with BRCA1 SNP were found to be lower than the DCNP reacting with normal (non-mutant) BRCA1 gene. We also demonstrate that SP characteristics of DCNP with different substrates (e.g., Au, Si, SiO2, and Fe) provide us with a chance to attenuate or augment the SP signal of DCNP without additional enhancement of instrumentation capabilities.
机译:开尔文探针力显微镜(KPFM)是一个健壮分析表面电位(SP)的工具包生物分子dna之间的相互作用和/或在单分子水平的蛋白质。它经常遭受了背景噪声和由于仪器或低吞吐量环境约束,这被认为是限制KPFM检测申请分钟等分子结构的变化单核苷酸多态性(SNP)。显示KPFM DNA-capped纳米粒子的成像(DCNP),使BRCA1基因的SNP检测基因由于sterically适应dna dna限制内发生的交互DCNP的空间。与BRCA1 SNP交互被发现更低比DCNP反应与正常(non-mutant)BRCA1基因。DCNP不同基质的特点(例如,非盟、硅、二氧化硅,和铁)给我们提供了一个的SP信号减弱或增强的机会DCNP没有额外的增强仪表功能。

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