4.6 Article

A smart surface in a microfluidic chip for controlled protein separation

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CHEMISTRY-A EUROPEAN JOURNAL
卷 13, 期 18, 页码 5113-5120

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200601624

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cyclic voltammetry; microfluidic chips; proteins; self-assembly; smart surfaces

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The smart surface created in a microfluidic chip has shown the capability of adsorbing and releasing proteins under electrical control. ne inner surface of the chip channel was first coated by a thin layer of An through sputtering and was subsequently modified with loosely packed self-assembled monolayers (SAMs) of thiols with terminal carboxylic or amino groups. Upon application of an external electric potential to the gold substrate, reversible conformational transformation between bent and straight states for the anchored mercapto chains could be modulated, through the electrostatic effect between the ionized terminal groups and the charged gold substrate. Thus, a hydrophobic or hydrophilic channel surface was established and could be reversibly switched electrochemically. Accordingly, the microchips prepared in this way can reversibly and selectively adsorb and release differently charged proteins under electrical control. Two model proteins, avidin and streptavidin, were demonstrated to be readily adsorbed by the smart chips under negative and positive potential, respectively. Also, more than 90% of the adsorbed proteins could be released upon an electrical command. Furthermore, these chips were applied to the controlled separation of avidin and streptavidin mixtures with 1:1 and 1:1000 molar ratios. Under specific applied potentials, the chips adsorbed a certain protein from the mixture whereas the other protein was allowed to flow out, after which the adsorbed protein could be released by switching the applied potential. Thus, two eluted protein tractions were obtained and the separation of the two proteins was achieved. For the former mixture, each eluted fraction contained up to approximate to 80-90% avidin or streptavidin. For the latter mixture, the resulting separation efficiency indicated that the molar ratio of avidin and streptavidin could be increased from 1:1000 to about 32:1 after five run separations.

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