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Effect of ionic strength on PNA-DNA hybridization on surfaces and in solution

机译:离子强度对表面和溶液中PNA-DNA杂交的影响

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Peptide nucleic acids (PNAs) are mimics of oligonucleotides containing a neutral peptidelike backbone and are able to bind complementary DNA targets with high affinity and selectivity. In order to investigate the effect of the ionic strength of the buffer solution, hybridization experiments with PNAs as (catcher) probes and DNAs as target oligonucleotides were performed in different salt solutions. Surface plasmon field-enhanced fluorescence spectroscopy was employed for real-time monitoring of DNA hybridizations to surface bound PNA. Probes with three different strand lengths were immobilized by self-assembly on the sensor surface. By introducing Cy5-labeled DNA targets the affinity constants, KA=kon (association)/koff (dissociation), were determined for fully complementary (MM0) as well as for single base mismatched (MM1) duplexes. Furthermore, the thermal stability of each duplex was determined by measuring melting curves in solution which was then compared to the kinetic and affinity parameters determined for the surface hybridization reactions. The results indicate that ions do not play a significant role for the PNA/DNA hybridization kinetics at surfaces. However, changes in the configuration of the PNA/DNA duplex due to the ionic strength variations influence the fluorescence yield drastically.
机译:肽核酸(PNA)是含有中性肽样骨架的寡核苷酸的模拟物,能够以高亲和力和选择性结合互补的DNA靶标。为了研究缓冲溶液离子强度的影响,在不同的盐溶液中进行了以PNA作为(捕获)探针和DNA为靶寡核苷酸的杂交实验。表面等离激元场增强荧光光谱用于实时监测与表面结合的PNA的DNA杂交。通过自组装将具有三种不同链长的探针固定在传感器表面上。通过导入Cy5标记的DNA靶标,可以确定完全互补(MM0)和单碱基错配(MM1)双链体的亲和常数KA = kon(缔合)/ koff(解离)。此外,通过测量溶液中的熔解曲线来确定每个双链体的热稳定性,然后将其与为表面杂交反应确定的动力学和亲和力参数进行比较。结果表明离子对表面的PNA / DNA杂交动力学没有重要作用。但是,由于离子强度的变化,PNA / DNA双链体的构型变化会极大地影响荧光产量。

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