Biofunctional Nanomaterials Unit, CICbiomaGUNE, Paseo Miramon 182, 20009 San Sebastian, Spain.
Chemistry. 2010 Nov 22;16(44):13163-75. doi: 10.1002/chem.201001295.
An effective chemoenzymatic strategy is reported that has allowed the construction, for the first time, of a focused microarray of synthetic N-glycans. Based on modular approaches, a variety of N-glycan core structures have been chemically synthesized and covalently immobilized on a glass surface. The printed structures were then enzymatically diversified by the action of three different glycosyltransferases in nanodroplets placed on top of individual spots of the microarray by a printing robot. Conversion was followed by lectin binding specific for the terminal sugars. This enzymatic extension of surface-bound ligands in nanodroplets reduces the amount of precious glycosyltransferases needed by seven orders of magnitude relative to reactions carried out in the solution phase. Moreover, only those ligands that have been shown to be substrates to a specific glycosyltransferase can be individually chosen for elongation on the array. The methodology described here, combining focused modular synthesis and nanoscale on-chip enzymatic elongation, could open the way for the much needed rapid construction of large synthetic glycan arrays.
报道了一种有效的化学酶学策略,该策略首次实现了合成 N-聚糖的聚焦微阵列的构建。基于模块化方法,已通过化学方法合成了各种 N-聚糖核心结构,并将其共价固定在玻璃表面上。然后,通过打印机器人将三种不同的糖基转移酶置于微阵列各个点的纳米液滴中,使打印结构在纳米液滴中通过酶促反应进行多样化。通过与末端糖特异性结合的凝集素进行转化。与在溶液相中进行的反应相比,这种在纳米液滴中延伸表面结合配体的酶促反应将所需的宝贵糖基转移酶的数量减少了七个数量级。此外,只有那些已被证明是特定糖基转移酶底物的配体才能被单独选择用于在阵列上的延伸。此处描述的方法结合了集中式模块合成和纳米级芯片上的酶促延伸,为急需的快速构建大型合成聚糖阵列开辟了道路。