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用于基于阵列的应用(包括表面等离子体共振成像)的蛋白质连续流微流控打印。

Continuous-flow microfluidic printing of proteins for array-based applications including surface plasmon resonance imaging.

作者信息

Natarajan Sriram, Katsamba Phini S, Miles Adam, Eckman Josh, Papalia Giuseppe A, Rich Rebecca L, Gale Bruce K, Myszka David G

机构信息

Department of Chemical Engineering, University of Utah, Salt Lake City, UT 84132, USA.

出版信息

Anal Biochem. 2008 Feb 1;373(1):141-6. doi: 10.1016/j.ab.2007.07.035. Epub 2007 Aug 19.

Abstract

Arraying proteins is often more challenging than creating oligonucleotide arrays. Protein concentration and purity can severely limit the capacity of spots created by traditional pin and ink jet printing techniques. To improve protein printing methods, we have developed a three-dimensional microfluidic system to deposit protein samples within discrete spots (250-microm squares) on a target surface. Our current technology produces a 48-spot array within a 0.5 x 1 cm target area. A chief advantage of this method is that samples may be introduced in continuous flow, which makes it possible to expose each spot to a larger volume of sample than would be possible with standard printing methods. Using Biacore Flexchip (Biacore AB) surface plasmon resonance array-based biosensor as a chip reader, we demonstrate that the microfluidic printer is capable of spotting proteins that are dilute (<0.1 microg/ml) and contain high concentrations of contaminating protein (>10,000-fold molar excess). We also show that the spots created by the microfluidic printer are more uniform and have better-defined borders than what can be achieved with pin printing. The ability to readily print proteins using continuous flow will help expand the application of protein arrays.

摘要

排列蛋白质通常比创建寡核苷酸阵列更具挑战性。蛋白质的浓度和纯度会严重限制传统针式和喷墨打印技术所形成斑点的容量。为了改进蛋白质打印方法,我们开发了一种三维微流体系统,用于在目标表面的离散斑点(250微米见方)内沉积蛋白质样品。我们目前的技术在0.5×1厘米的目标区域内产生一个48斑点的阵列。这种方法的一个主要优点是样品可以连续流动引入,这使得每个斑点能够接触到比标准打印方法更多体积的样品。使用基于Biacore Flexchip(Biacore AB)表面等离子体共振阵列的生物传感器作为芯片读取器,我们证明微流体打印机能够点样稀释的蛋白质(<0.1微克/毫升)且含有高浓度污染蛋白质(摩尔过量>10000倍)。我们还表明,微流体打印机产生的斑点比针式打印的更均匀,边界更清晰。使用连续流动轻松打印蛋白质的能力将有助于扩大蛋白质阵列的应用。

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