Orosco Manuel M, Pacholski Claudia, Sailor Michael J
Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, Department 0358, La Jolla, California 92093-0358, USA.
Nat Nanotechnol. 2009 Apr;4(4):255-8. doi: 10.1038/nnano.2009.11. Epub 2009 Feb 22.
The activity of certain proteolytic enzymes is often an indicator of disease states such as cancer, stroke and neurodegeneracy, so there is a need for rapid assays that can characterize the kinetics and substrate specificity of enzymatic reactions. Nanostructured membranes can efficiently separate biomolecules, but coupling a sensitive detection method to such a membrane remains difficult. Here, we demonstrate a single mesoporous nanoreactor that can isolate and quantify in real time the reaction products of proteases. The reactor consists of two layers of porous films electrochemically prepared from crystalline silicon. The upper layer, with large pore sizes ( approximately 100 nm in diameter), traps the protease and acts as the reactor. The lower layer, with smaller pore sizes ( approximately 6 nm), excludes the proteases and other large proteins and captures the reaction products. Infiltration of the digested fragments into the lower layer produces a measurable change in optical reflectivity, and this allows label-free quantification of enzyme kinetics in real time within a volume of approximately 5 nl.
某些蛋白水解酶的活性通常是癌症、中风和神经退行性疾病等疾病状态的指标,因此需要能够表征酶促反应动力学和底物特异性的快速检测方法。纳米结构膜可以有效地分离生物分子,但将灵敏的检测方法与此类膜相结合仍然很困难。在这里,我们展示了一种单一的介孔纳米反应器,它可以实时分离和定量蛋白酶的反应产物。该反应器由两层通过电化学方法由晶体硅制备的多孔膜组成。上层具有较大的孔径(直径约100纳米),捕获蛋白酶并充当反应器。下层具有较小的孔径(约6纳米),可排除蛋白酶和其他大蛋白,并捕获反应产物。消化片段渗入下层会导致光学反射率发生可测量的变化,这使得能够在约5纳升的体积内实时对酶动力学进行无标记定量。