Fraunhofer Institute for Biomedical Engineering, Department of Nanobiotechnology and Nanomedicine, Am Mühlenberg 13, 14476 Potsdam, Germany.
J Nanobiotechnology. 2010 May 17;8:10. doi: 10.1186/1477-3155-8-10.
Micrometer resolution placement and immobilization of probe molecules is an important step in the preparation of biochips and a wide range of lab-on-chip systems. Most known methods for such a deposition of several different substances are costly and only suitable for a limited number of probes. In this article we present a flexible procedure for simultaneous spatially controlled immobilization of functional biomolecules by molecular ink lithography.
For the bottom-up fabrication of surface bound nanostructures a universal method is presented that allows the immobilization of different types of biomolecules with micrometer resolution. A supporting surface is biotinylated and streptavidin molecules are deposited with an AFM (atomic force microscope) tip at distinct positions. Subsequent incubation with a biotinylated molecule species leads to binding only at these positions. After washing streptavidin is deposited a second time with the same AFM tip and then a second biotinylated molecule species is coupled by incubation. This procedure can be repeated several times. Here we show how to immobilize different types of biomolecules in an arbitrary arrangement whereas most common methods can deposit only one type of molecules. The presented method works on transparent as well as on opaque substrates. The spatial resolution is better than 400 nm and is limited only by the AFM's positional accuracy after repeated z-cycles since all steps are performed in situ without moving the supporting surface. The principle is demonstrated by hybridization to different immobilized DNA oligomers and was validated by fluorescence microscopy.
The immobilization of different types of biomolecules in high-density microarrays is a challenging task for biotechnology. The method presented here not only allows for the deposition of DNA at submicrometer resolution but also for proteins and other molecules of biological relevance that can be coupled to biotin.
将探针分子以微米级分辨率放置和固定是生物芯片和各种微流控芯片系统制备的重要步骤。大多数已知的用于沉积多种不同物质的方法成本高昂,并且仅适用于有限数量的探针。在本文中,我们提出了一种通过分子墨水光刻术同时进行空间控制的固定功能生物分子的灵活程序。
为了进行基于自下而上的表面结合纳米结构的制造,提出了一种通用方法,该方法允许以微米级分辨率固定不同类型的生物分子。将支撑表面进行生物素化,并且通过原子力显微镜(AFM)尖端在不同位置沉积链霉亲和素分子。随后在这些位置与生物素化分子物种孵育导致仅在这些位置结合。洗涤后,用相同的 AFM 尖端再次沉积链霉亲和素,然后通过孵育将第二种生物素化分子物种偶联。该过程可以重复几次。在这里,我们展示了如何以任意排列固定不同类型的生物分子,而大多数常见的方法只能沉积一种类型的分子。该方法适用于透明和不透明的基底。空间分辨率优于 400nm,并且仅受 AFM 重复 z 循环后的位置精度限制,因为所有步骤都是在原位进行的,而无需移动支撑表面。该原理通过与不同固定化 DNA 寡聚物的杂交得到证明,并通过荧光显微镜进行了验证。
在高密度微阵列中固定不同类型的生物分子是生物技术面临的一项挑战。这里提出的方法不仅允许亚微米分辨率的 DNA 沉积,还允许与生物素偶联的蛋白质和其他具有生物学相关性的分子沉积。