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Immobilization-mediated reduction in melting temperatures of DNA-DNA and DNA-RNA hybrids: Immobilized DNA probe hybridization studied by SPR

机译:固定化介导的DNA-DNA和DNA-RNA杂种熔解温度的降低:SPR研究的固定化DNA探针杂交

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The melting temperature of probe-target nucleic acid hybrids plays an important role in sensor performance. This study employed surface plasmon resonance (SPR) techniques to investigate the hybridization of both DNA and RNA targets to their complementary surface-bound DNA oligonucleotide and the corresponding melting temperatures. The target molecule was a 26 nucleotide strand of RNA selected because of its utility in detecting the tobacco mosaic virus, a common plant pathogen with an RNA genome. The melting temperatures of duplexes with immobilized probes were determined by hybridization of the DNA and RNA targets with the bound DNA probe at different temperatures using a custom-built thermostated dual-channel SPR cell. Hybridization conditions and binding efficiencies were compared for both DNA and RNA binding to the gold-coated surface-bound DNA probe. The melting temperature for the DNA-DNA duplex was approximately 15 degrees C higher than the DNA-RNA in the solid state. The melting temperature in solution was also measured for comparison to the surface values. For both RNA and DNA, the melting transitions were substantially lower (similar to 20 degrees C) for solid state binding relative to solution. Particularly for surface immobilized DNA-RNA hybrids, the melting temperature was reduced to room temperature or below. Since most biosensor platforms operate at room temperature, they may consequently exhibit poor sensor performance due to weakened probe-target interactions. This result emphasizes that for optimal sensor performance, the hybrid melting temperature should be considered. The ability to study and optimize the binding of complementary strands of genomic materials to bound DNA probes could facilitate the rapid detection and identification of plant viruses having genomic RNA using various biosensor rapid analytical techniques. (C) 2015 Elsevier B.V. All rights reserved.
机译:探针-目标核酸杂交体的解链温度在传感器性能中起着重要作用。这项研究采用表面等离振子共振(SPR)技术来研究DNA和RNA靶标与其互补的表面结合DNA寡核苷酸的杂交以及相应的解链温度。选择目标分子是一条26核苷酸的RNA链,因为它可用于检测烟草花叶病毒(一种具有RNA基因组的常见植物病原体)。使用定制的恒温双通道SPR细胞,通过在不同温度下将DNA和RNA靶标与结合的DNA探针杂交,可以确定具有固定探针的双链体的解链温度。比较了DNA和RNA与镀金表面结合DNA探针结合的杂交条件和结合效率。 DNA-DNA双链体的解链温度比固态DNA-RNA高约15摄氏度。还测量溶液中的熔融温度以与表面值比较。对于RNA和DNA而言,固态结合相对于溶液而言,其熔解转变明显较低(类似于20摄氏度)。特别是对于表面固定化的DNA-RNA杂化物,其解链温度降低到室温或更低。由于大多数生物传感器平台都在室温下运行,因此由于探针与目标之间的相互作用减弱,它们可能会表现出较差的传感器性能。该结果强调,为获得最佳传感器性能,应考虑混合熔化温度。研究和优化基因组材料互补链与结合的DNA探针的结合的能力可以促进使用各种生物传感器快速分析技术快速检测和鉴定具有基因组RNA的植物病毒。 (C)2015 Elsevier B.V.保留所有权利。

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