Lockett Matthew R, Shortreed Michael R, Smith Lloyd M
Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, USA.
Langmuir. 2008 Sep 2;24(17):9198-203. doi: 10.1021/la800991t. Epub 2008 Aug 2.
Amorphous carbon thin films are easily deposited at room temperature, readily functionalized with alkene-containing molecules through a UV photochemical reaction, and provide a robust surface capable of supporting chemical and biomolecule array fabrication. Aldehyde-terminated amorphous carbon substrates were fabricated via the attachment of a 2-(10-undecen-1-yl)-1,3-dioxolane molecule. The surfaces were then deprotected in 1.5 M HCl to yield an aldehyde-terminated surface that is readily reactive with amine containing molecules. An array of amine-modified oligonucleotides was prepared on aldehyde-terminated surfaces prepared on both amorphous carbon and on gold self-assembled monolayers, and the fluorescence background, feature signal-to-noise ratio, and hybridization densities were compared. The aldehyde-terminated amorphous carbon substrates offer inherently lower background fluorescence intensity and a greater number of hybridization-accessible sites.
非晶碳薄膜在室温下易于沉积,通过紫外光化学反应可轻松与含烯烃分子进行功能化,并且能提供一个坚固的表面,可支持化学和生物分子阵列的制备。通过连接2-(10-十一碳烯-1-基)-1,3-二氧戊环分子制备了醛基封端的非晶碳基底。然后将表面在1.5 M盐酸中脱保护,以产生易于与含胺分子反应的醛基封端表面。在非晶碳和金自组装单分子层上制备的醛基封端表面上制备了一系列胺修饰的寡核苷酸,并比较了荧光背景、特征信噪比和杂交密度。醛基封端的非晶碳基底具有固有的较低背景荧光强度和更多的杂交可及位点。