Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada.
Biomaterials. 2010 Jan;31(2):315-20. doi: 10.1016/j.biomaterials.2009.09.040. Epub 2009 Oct 2.
We present a straightforward, accessible method to covalently pattern proteins in poly(dimethyl siloxane) (PDMS) microchannels. Our approach includes (i) region-specific photografting of a layer of poly(acrylamide) (PAAm) and (ii) bioconjugation of PAAm with a desired protein. The method produces symmetric protein patterns on all channel walls, which have high specificity and pattern fidelity, are compatible with a variety of geometries and exhibit excellent longevity under shear stresses of up to 1 dyn/cm. We demonstrate the generality of the method by creating multi-protein gradients within microfluidic microchannels and by in-situ patterning of islands of multiple proteins. Protein activity was observed by the digestion of BODIPY-casein using channels patterned with trypsin.
我们提出了一种简单、可行的方法,可将蛋白质在聚二甲基硅氧烷(PDMS)微通道中进行共价图案化。我们的方法包括(i)聚(丙烯酰胺)(PAAm)的区域特异性光接枝,以及(ii)与所需蛋白质的生物偶联。该方法在所有通道壁上产生对称的蛋白质图案,具有高特异性和图案保真度,与各种几何形状兼容,并在高达 1 dyn/cm 的剪切应力下具有出色的耐久性。我们通过在微流控微通道内创建多种蛋白质梯度以及通过原位图案化多个蛋白质岛来证明该方法的通用性。通过使用胰蛋白酶图案化的通道,观察到 BODIPY-酪蛋白的消化来证明蛋白质的活性。