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Creation of a functional heterogeneous vesicle array via DNA controlled surface sorting onto a spotted microarray

机译:通过将DNA控制的表面分选到斑点微阵列上来创建功能性异质囊泡阵列

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Membrane protein microarrays are expected to play a key role in the future of drug screening and discovery. The authors present a method for the creation of functional heterogeneous vesicle arrays via DNA controlled surface sorting. Complexes of streptavidin and biotinylated DNA are spotted onto a biomolecule- and cell-resistant surface of biotinylated poly(l-lysine)-grafted-poly(ethylene glycol). Two kinds of vesicles functionalized with either the membrane-binding protein annexin A5 or loaded with bovine serum albumin, are tagged with DNA, mixed together, and guided to predefined spots on the surface. The authors show that the spotted complexes remain active and selective and that the background is resistant towards nonspecific adsorption of the vesicles and the proteins.
机译:膜蛋白微阵列有望在未来的药物筛选和发现中发挥关键作用。作者提出了一种通过DNA控制的表面分选创建功能性异质囊泡阵列的方法。将链霉亲和素和生物素化的DNA的复合物点到生物素化的聚(1-赖氨酸)-接枝的聚(乙二醇)的抗生物分子和细胞的表面上。用膜结合蛋白膜联蛋白A5或牛血清白蛋白功能化的两种囊泡用DNA标记,混合在一起,并引导至表面上预定的斑点。作者表明,斑点复合物保持活性和选择性,并且背景对囊泡和蛋白质的非特异性吸附具有抵抗力。

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