Bujoli Bruno, Lane Sarah M, Nonglaton Guillaume, Pipelier Muriel, Léger Jean, Talham Daniel R, Tellier Charles
Laboratoire de Synthèse Organique, UMR CNRS 6513 & FR CNRS 2465, 2 Rue de la Houssinière, BP92208, 44322 Nantes Cedex 03, France.
Chemistry. 2005 Mar 18;11(7):1980-8. doi: 10.1002/chem.200400960.
A new process for preparing oligonucleotide arrays is described that uses surface grafting chemistry which is fundamentally different from the electrostatic adsorption and organic covalent binding methods normally employed. Solid supports are modified with a mixed organic/inorganic zirconium phosphonate monolayer film providing a stable, well-defined interface. Oligonucleotide probes terminated with phosphate are spotted directly on to the zirconated surface forming a covalent linkage. Specific binding of terminal phosphate groups with minimal binding of the internal phosphate diesters has been demonstrated. The mixed organic/inorganic thin films have also been extended for use arraying DNA duplex probes, and therefore represent a viable general approach to DNA-based bioarrays. Ideas for interfacing mixed organic/inorganic interfaces to other bioapplications are also discussed.
描述了一种制备寡核苷酸阵列的新方法,该方法使用的表面接枝化学与通常采用的静电吸附和有机共价结合方法有根本区别。固体支持物用有机/无机混合的磷酸锆单层膜进行修饰,从而提供一个稳定、明确的界面。末端带有磷酸基团的寡核苷酸探针直接点样到锆化表面上,形成共价连接。已证明末端磷酸基团的特异性结合以及内部磷酸二酯的最小结合。有机/无机混合薄膜也已扩展用于排列DNA双链体探针,因此代表了一种可行的基于DNA的生物阵列通用方法。还讨论了将有机/无机混合界面与其他生物应用相连接的思路。