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在通道内玻璃纤维上的氧化石墨烯和壳聚糖的层层涂层中固定化胰蛋白酶,用于微流控蛋白水解。

Immobilization of trypsin in the layer-by-layer coating of graphene oxide and chitosan on in-channel glass fiber for microfluidic proteolysis.

机构信息

School of Pharmacy, Department of Chemistry, Fudan University, Shanghai, PR China.

出版信息

Analyst. 2011 Dec 21;136(24):5190-6. doi: 10.1039/c1an15690j. Epub 2011 Oct 19.

Abstract

In this report, trypsin was immobilized in the layer-by-layer (LBL) coating of graphene oxide (GO) and chitosan on a piece of glass fiber to fabricate microchip bioreactor for efficient proteolysis. LBL deposition driven by electrostatic forces easily took place on the surface of the glass fiber, providing mild environmental conditions so that the denaturation and autolysis of the immobilized trypsin was minimized. Prior to use, a piece of the prepared trypsin-immobilized glass fiber was inserted into the channel of a microchip to form a core-changeable bioreactor. The novel GO-based bioreactor can be regenerated by changing its fiber core. The feasibility and performance of the unique bioreactor were demonstrated by the tryptic digestion of bovine serum albumin, myoglobin, cytochrome c, and hemoglobin and the digestion time was significantly reduced to less than 10 s. The obtained digests were identified by MALDI-TOF MS. The digestion performance of the core-changeable GO-based microchip bioreactor was comparable to that of 12-h in-solution tryptic digestion. The novel microchip bioreactor is simple and efficient, offering great promise for high-throughput protein identification.

摘要

在本报告中,胰蛋白酶被固定在氧化石墨烯(GO)和壳聚糖的层层(LBL)涂层中,然后涂覆在玻璃纤维上,以构建用于有效蛋白水解的微芯片生物反应器。通过静电力驱动的 LBL 沉积很容易在玻璃纤维表面发生,从而提供温和的环境条件,使固定化胰蛋白酶的变性和自溶最小化。在使用之前,将一块制备好的固定化胰蛋白酶玻璃纤维插入微芯片的通道中,形成可更换纤维核的生物反应器。新型基于 GO 的生物反应器可以通过更换纤维核来进行再生。通过牛血清白蛋白、肌红蛋白、细胞色素 c 和血红蛋白的胰蛋白酶消化来验证独特生物反应器的可行性和性能,消化时间显著缩短至 10 秒以内。通过 MALDI-TOF MS 对获得的消化产物进行鉴定。可更换纤维核的 GO 基微芯片生物反应器的消化性能可与 12 小时溶液内胰蛋白酶消化相媲美。新型微芯片生物反应器简单高效,有望实现高通量蛋白质鉴定。

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