Department of Biological Chemistry, Indian Association for the Cultivation of Science , Jadavpur, Kolkata-700 032, India.
Langmuir. 2013 Sep 24;29(38):11982-90. doi: 10.1021/la4019579. Epub 2013 Sep 16.
Unambiguous identification of single base mismatches in nucleic acid sequences is of great importance in nucleic acid detection assays. However, ambiguities are often encountered with, and therefore, a strategy for attaining substantially large enhancement of mismatch discrimination has been worked upon in this study. Short single-stranded peptide nucleic acid (PNA) and deoxyribonucleic acid (DNA) sensor probes that are immobilized onto gold nanoparticle (AuNP) modified Au(111) surface have been applied for target DNA detection. It will be shown that while both PNA and the analogous DNA probes exhibit generally better target detection abilities on the AuNP-modified Au(111) surface (elicited from fluorescence-based measurement of on-surface Tm values), compared to the bare Au(111) surface, PNA supersedes DNA, for all sizes of AuNPs (10, 50, and 90 nm) applied, with the difference being quite drastic in the case of the smallest 10 nm AuNP. It is found that while the AuNP curvature plays a pivotal role in target detection abilities of the PNA probes, the changes in the surface roughness caused by AuNP treatment do not exert any significant influence. This study also presents a means for preparing PNA-AuNP hybrids without altering PNA functionality and without AuNP aggregation by working with the surface-affixed AuNPs.
在核酸检测中,明确识别核酸序列中的单碱基错配非常重要。然而,经常会遇到这种情况,因此,本研究旨在制定一种策略,以实现对错配的显著增强识别。本研究应用固定在金纳米粒子(AuNP)修饰的 Au(111)表面上的短单链肽核酸(PNA)和脱氧核糖核酸(DNA)传感器探针,用于目标 DNA 的检测。结果表明,与裸 Au(111)表面相比,尽管 PNA 和类似的 DNA 探针在 AuNP 修饰的 Au(111)表面上(通过表面 Tm 值的荧光测量得出)通常表现出更好的目标检测能力,但 PNA 优于 DNA,适用于所有大小的 AuNP(10、50 和 90nm),在最小的 10nm AuNP 情况下,差异非常明显。研究发现,虽然 AuNP 曲率在 PNA 探针的目标检测能力中起着关键作用,但 AuNP 处理引起的表面粗糙度变化并没有产生任何显著影响。本研究还提出了一种制备 PNA-AuNP 杂化物的方法,该方法无需改变 PNA 的功能,也无需通过表面固定的 AuNP 进行 AuNP 聚集。