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Nanofluidic molecular filters for efficient protein separation and preconcentration

机译:纳米流体分子过滤器,用于有效蛋白质分离和前​​浓度

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Regular nanofluidic channels, as thin as 20 nm, have been fabricated and used for protein separation and preconcentration. The nanochannels were fabricated by the substrate-bonding method, and the regularity of the nanochannel has been confirmed by cross-section SEM imaging. A nanofilter array device, with an array of 60-120 nm thin nanofilters, was used for separating small biomolecules (short double-stranded DNA and SDS-coated proteins) based on their size. The sieving of biomolecules (which are comparable to or smaller than the nanofilter gap size) is achieved by steric hindrance of biomolecules within nanochannels. The efficiency of this gel-free separation device is comparable to capillary gel electrophoresis, and can be made better by further optimization. In addition, we have developed a novel biomolecule concentrator using a 40 nm nanofluidic channel as a perm-selective membrane. More than a million times preconcentration of dilute protein or peptide solutions was demonstrated, which was enabled by the stability of the device.
机译:已经制造了常规纳米流体通道,薄为20nm,并用于蛋白质分离和前​​浓缩。通过基板键合方法制造纳米槽,并且通过横截面SEM成像证实了纳米通道的规律性。具有60-120nm薄纳米过滤器阵列的纳入过滤器阵列装置,用于基于其尺寸分离小的生物分子(短链双链DNA和SDS涂覆的蛋白质)。通过纳米纳米内的生物分子的空间阻断来实现生物分子的筛分(其与纳米过滤间隙尺寸相当)。这种无凝胶分离装置的效率与毛细血管凝胶电泳相当,并且可以通过进一步的优化来更好地实现。此外,我们已经开发了一种新的生物分子浓缩器,其使用40nm纳米流体通道作为渗透选择性膜。证明了稀释蛋白质或肽溶液的预浓缩的超过一百万次,这是通过装置的稳定性实现的。

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