Hasenbank Melissa S, Edwards Thayne, Fu Elain, Garzon Richard, Kosar T Fettah, Look Michael, Mashadi-Hossein Afshin, Yager Paul
Department of Bioengineering, University of Washington, Seattle, WA 98195, United States.
Anal Chim Acta. 2008 Mar 17;611(1):80-8. doi: 10.1016/j.aca.2008.01.048. Epub 2008 Feb 2.
Patterning substrates with biological reagents is a critical component of biosensor development. Many applications require multi-analyte patterning capabilities, with a need to deposit several species reproducibly with a high degree of precision. We demonstrate a piezoelectric inkjet printing system that is capable of creating sub-millimeter (down to 150microm) patterns of aqueous and nonaqueous reagents with precise placement for biosensor applications. The size, shape, and density of the patterns may be modified by simple adjustments of the patterning parameters. Using this system, two methods of multi-analyte protein patterning for use in biosensor assays are demonstrated. The first method involves the deposition of multiple proteins directly onto a gold substrate. Specific binding of an antibody to the deposited antigen is demonstrated, although nonspecific adsorption of the antibody may limit the utility of this simple method in quantitative biosensor applications. A second, more sophisticated multi-analyte patterning method involves two sequential patterning steps, consisting of an initial deposition onto gold of a mixed thiol layer to provide oriented binding capabilities in a nonfouling background and a second deposition of multiple biotinylated proteins. Highly specific antibody binding to this patterned multi-analyte surface was demonstrated, with minimal nonspecific adsorption to the surrounding regions. Thus, this method produces high-quality, localized, and customizable sub-millimeter patterns in a nonfouling background for multi-analyte bioassay development.
用生物试剂对基底进行图案化是生物传感器开发的关键组成部分。许多应用需要多分析物图案化能力,即需要以高精度可重复地沉积多种物质。我们展示了一种压电喷墨打印系统,该系统能够为生物传感器应用创建水性和非水性试剂的亚毫米(低至150微米)图案,并实现精确放置。通过简单调整图案化参数,可以改变图案的尺寸、形状和密度。利用该系统,展示了两种用于生物传感器检测的多分析物蛋白质图案化方法。第一种方法是将多种蛋白质直接沉积到金基底上。尽管抗体的非特异性吸附可能会限制这种简单方法在定量生物传感器应用中的效用,但仍证明了抗体与沉积抗原的特异性结合。第二种更复杂的多分析物图案化方法包括两个连续的图案化步骤,首先在金上沉积一层混合硫醇层,以在无污背景中提供定向结合能力,然后再沉积多种生物素化蛋白质。已证明抗体与这种图案化的多分析物表面具有高度特异性结合,对周围区域的非特异性吸附极少。因此,该方法在无污背景中为多分析物生物检测开发生成高质量、局部化且可定制的亚毫米图案。