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通过原位滚环扩增在聚(丙烯酸)刷涂多孔硅上制造 DNA 微阵列。

DNA microarray fabricated on poly(acrylic acid) brushes-coated porous silicon by in situ rolling circle amplification.

机构信息

State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, Jiangsu, PR China.

出版信息

Analyst. 2012 Oct 7;137(19):4539-45. doi: 10.1039/c2an35417a.

Abstract

Microarrays hold considerable promise in large-scale biology on account of their analytical, massive and parallel nature. In a step toward further enabling such a capability, we describe the application of rolling circle amplification (RCA) for a sensitive and multiplex detection of nucleic acid targets on oligonucleotide-conjugated polymer brushes covalently grown from porous silicon. Both RCA and polymer brushes have been taken to increase the loading quantity of target molecules and thus improve the detection sensitivity without loss of multiplexing. Besides, polymer brushes were employed to protect porous silicon and to provide biologically simulated environments, making the attached biomolecules maintain bioactivity. This approach can reach a detection limit of 0.1 nM target analytes and three orders of magnitude dynamic range of 0.1-100 nM, with a fluorescence scanner. A two-colour DNA microarray was achieved via RCA of two kinds of circular DNA targets on one chip simultaneously. The porous silicon chip-based RCA technique is promising for the multiplex detection of deoxynucleic acids on microarrays.

摘要

微阵列在大规模生物学中具有很大的应用前景,因为它们具有分析、大规模和并行的特点。为了进一步实现这一功能,我们描述了滚环扩增(RCA)在寡核苷酸偶联聚合物刷上对核酸靶标的敏感和多重检测中的应用,该聚合物刷通过多孔硅共价生长。RCA 和聚合物刷都被用来增加目标分子的负载量,从而在不损失多重检测的情况下提高检测灵敏度。此外,聚合物刷被用来保护多孔硅并提供模拟生物环境,使附着的生物分子保持生物活性。该方法可以用荧光扫描仪达到 0.1 nM 目标分析物的检测限和 0.1-100 nM 的三个数量级动态范围。通过在一个芯片上同时对两种环状 DNA 靶标进行 RCA,实现了双色 DNA 微阵列。基于多孔硅芯片的 RCA 技术有望用于微阵列上脱氧核酸的多重检测。

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