Song Xuezheng, Xia Baoyun, Lasanajak Yi, Smith David F, Cummings Richard D
Department of Biochemistry, Emory University School of Medicine, O. Wayne Rollins Research Center, 1510 Clifton Road, Suite 4001, Atlanta, GA 30322, USA.
Glycoconj J. 2008 Jan;25(1):15-25. doi: 10.1007/s10719-007-9066-8. Epub 2007 Sep 1.
A glycan microarray was developed by using 2,6-diaminopyridine (DAP) as a fluorescent linker and printing of the glycan-DAP conjugates (GDAPs) on epoxy-activated glass slides. Importantly, all coupled GDAPs showed a detectable level of concentration-dependent GDAP fluorescence under blue laser excitation (495 nm) that can be used for both grid location and on-slide quantification. A glycan array including a large number of GDAP's derived from natural and commercially available free glycans was constructed and glycan interactions with various plant lectins were investigated. In addition, binding parameters of lectins to glycans were obtained by varying both the amount of GDAPs on the array and the lectin concentration in analyses. These data demonstrate the general utility of GDAP microarrays for functional glycomic analyses and for determining binding parameters of glycan binding proteins (GBPs).
通过使用2,6-二氨基吡啶(DAP)作为荧光连接剂,并将聚糖-DAP缀合物(GDAPs)打印在环氧活化的载玻片上,开发了一种聚糖微阵列。重要的是,所有偶联的GDAPs在蓝色激光激发(495nm)下均显示出可检测水平的浓度依赖性GDAP荧光,可用于网格定位和载玻片上定量。构建了一个包含大量源自天然和市售游离聚糖的GDAPs的聚糖阵列,并研究了聚糖与各种植物凝集素的相互作用。此外,通过在分析中改变阵列上GDAPs的量和凝集素浓度,获得了凝集素与聚糖的结合参数。这些数据证明了GDAP微阵列在功能糖组学分析和确定聚糖结合蛋白(GBPs)结合参数方面的普遍实用性。