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Poly-L-histidine coated microfluidic devices for bacterial DNA purification without chaotropic solutions

机译:用于细菌DNA纯化的聚-L-组氨酸涂覆的微流体装置,没有椎间溶液溶解

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摘要

We present a disposable polymeric microfluidic device capable of reversibly binding and purifying Salmonella DNA through solid phase extraction (SPE). The microfluidic channels are first oxygen plasma treated and simultaneously micro-nanotextured, and then functionalized with amine groups via modification with L-histidine or poly-L-histidine. L-Histidine and poly-L-histidine bind on the plasma treated chip surface, and are not detached when rinsing with DNA purification protocol buffers. A pH-dependent protocol is applied on-chip to purify Salmonella DNA, which is first bound on the protonated amines at a pH (5.0) lower than their pKa of surface amine-groups which is 6.0 and then released at a pH higher than the pKa value (10.5). It was found that modification with poly-L-histidine resulted in higher surface density of amine groups onto microfluidic channel. Using the chip modified with poly-L-histidine, high recovery efficiency of at least 550 ng of isolated Salmonella DNA as well as DNA purification from Salmonella cell lysates corresponding to less than 5000 cells or 0.026 ng of Salmonella DNA was achieved. The protocol developed does not require ethanol or chaotropic solutions typically used in DNA purification, which are known inhibitors for downstream operations such as polymerase chain reactions (PCR) and which can also attack some polymeric microfluidic materials. Therefore, the microfluidic device and the related protocol hold promise for facile incorporation in microfluidics and Lab-on-a-chip (LOC) platforms for pathogen detection or in general for DNA purification.
机译:我们提出了一种可转化的聚合物微流体装置,其能够通过固相萃取(SPE)可逆地结合和纯化沙门氏菌DNA。微流体通道是第一种氧等离子体处理和同时微型纳米纹理,然后通过用L-组氨酸或多L-组氨酸改性用胺基官能化。 L-组氨酸和聚-L-组氨酸在等离子体处理的芯片表面上结合,并且在用DNA纯化方案缓冲液冲洗时不会脱离。贴上pH依赖性方案以涂上片上纯化沙门氏菌DNA,其首先在pH(5.0)的质子化胺上比其表面胺基的PKA在6.0的pKa上,然后在pH下释放到高于PKA值(10.5)。发现用聚L-组氨酸的改性导致胺基的表面密度较高,胺基在微流体通道上。使用用聚-L-组氨酸改性的芯片,实现了至少550ng分离的沙门氏菌DNA的高回收效率以及来自对应于小于5000个细胞或0.026ng沙门氏菌DNA的沙门氏菌细胞裂解物的DNA纯化。所开发的方案不需要通常用于DNA纯化的乙醇或混淆溶液,其是用于下游操作的已知抑制剂,例如聚合酶链反应(PCR),其也可以攻击一些聚合物微流体材料。因此,微流体装置和相关协议的承担承诺在微流体和芯片的实验室掺入(用于病原体检测的实验室平台中,或者通常用于DNA纯化。

著录项

  • 来源
    《Biomedical Microdevices》 |2020年第3期|44.1-44.12|共12页
  • 作者单位

    Institute of Nanoscience and Nanotechnology NCSR 'Demokritos' Patriarhou Gregoriou E' & 27 Neapoleos Str. 153 41 Aghia Paraskevi Attiki Greece Department of Chemistry University of Athens 157 71 Athens Greece;

    Institute of Nuclear & Radiological Sciences & Technology Energy & Safety NCSR 'Demokritos' Patriarhou Gregoriou E' & 27 Neapoleos Str. 153 41 Aghia Paraskevi Attiki Greece;

    Institute of Nanoscience and Nanotechnology NCSR 'Demokritos' Patriarhou Gregoriou E' & 27 Neapoleos Str. 153 41 Aghia Paraskevi Attiki Greece;

    Institute of Nanoscience and Nanotechnology NCSR 'Demokritos' Patriarhou Gregoriou E' & 27 Neapoleos Str. 153 41 Aghia Paraskevi Attiki Greece;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Plasma modification; High surface area; Amine groups; DNA purification; Microfluidics; Poly-L-histidine; L-histidine;

    机译:等离子体改性;高表面积;胺群;DNA纯化;微流体;聚L-组氨酸;l-组氨酸;

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