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Light-directed synthesis of peptide nucleic acids (PNAs) chips

机译:肽核酸(PNA)芯片的光导合成

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摘要

We report herein the light-directed synthesis of peptide nucleic acids (PNAs) microarray using PNA monomers protected by photolabile protecting groups and a maskless technique that uses a digital micromirror array system to form virtual masks. An ultraviolet image from the virtual mask was cast onto the active surface of a glass substrate, which was mounted in a flow cell reaction chamber connected to a peptide synthesizer. Light exposure was followed by automatic chemical coupling cycles and these steps were repeated with different virtual masks to grow the desired PNA probes in a selected pattern. In a preliminary experiment, an array of PNA probes with dimensions of 4.11 mm x 4.11 nim was generated on each slide. Each synthesis region in the final array measured 210 mu m x 210 mu m for a total of 256 sites. The center-to-center space was 260 mu m. It was observed from the hybridization pattern of the fluorescently labeled ofigonucleotide targets that the fluorescence intensities of the matched, and mismatched sequences showed substantial difference, demonstrating specificity in the identification of complementary sequences. This opens the way to exploit processes from the microelectronics industry for the fabrication of PNA microarrays with high densities. (c) 2006 Elsevier B.V. All rights reserved.
机译:我们在本文中报道了使用受光不稳定保护基团保护的PNA单体和使用数字微镜阵列系统形成虚拟掩模的无掩模技术对肽核酸(PNA)微阵列进行光导合成。将来自虚拟掩模的紫外线图像投射到玻璃基板的活性表面上,该玻璃基板安装在与肽合成仪相连的流通池反应室​​中。曝光后进行自动化学偶联循环,并使用不同的虚拟掩模重复这些步骤,以使所需的PNA探针以选定的模式生长。在初步实验中,在每个载玻片上生成了尺寸为4.11 mm x 4.11 nim的PNA探针阵列。最终阵列中每个合成区域的大小为210微米x 210微米,共256个位点。中心到中心的空间为260微米。从荧光标记的寡核苷酸靶的杂交模式观察到,匹配的和错配的序列的荧光强度显示出实质性的差异,证明了互补序列鉴定的特异性。这为利用微电子行业的工艺制造高密度PNA微阵列开辟了道路。 (c)2006 Elsevier B.V.保留所有权利。

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