Institute of Life Technologies, University of Applied Sciences Western Switzerland, Sion 1950, Switzerland.
Molecules. 2013 Aug 16;18(8):9833-49. doi: 10.3390/molecules18089833.
Several azide-derivatized and fluorescently-labeled peptides were immobilized on azadibenzocyclooctyne (ADIBO)-activated slide surfaces via a strain-promoted alkyne-azide cycloaddition (SPAAC) reaction revealing excellent immobilization kinetics, good spot homogeneities and reproducible fluorescence signal intensities. A myc-peptide micro-array immunoassay showed an antibody limit-of-detection (LOD) superior to a microtiter plate-based ELISA. Bovine serum albumin (BSA) and dextran covalently attached via "click" chemistry more efficiently reduced non-specific binding (NSB) of fluorescently-labeled IgG to the microarray surface in comparison to immobilized hexanoic acid and various types of polyethylene glycol (PEG) derivatives. Confirmation of these findings via further studies with other proteins and serum components could open up new possibilities for human sample and microarray platform-based molecular diagnostic tests.
几种叠氮化物衍生和荧光标记的肽通过应变促进的炔基-叠氮化物环加成(SPAAC)反应固定在氮杂二苯并环辛炔(ADIBO)激活的载玻片表面上,显示出优异的固定化动力学、良好的斑点均一性和可重复的荧光信号强度。一种 Myc 肽微阵列免疫分析显示,抗体检测限(LOD)优于基于微量滴定板的 ELISA。牛血清白蛋白(BSA)和葡聚糖通过“点击”化学共价结合,与固定化己酸和各种类型的聚乙二醇(PEG)衍生物相比,更有效地降低了荧光标记 IgG 与微阵列表面的非特异性结合(NSB)。通过进一步研究其他蛋白质和血清成分证实了这些发现,这为基于人类样本和微阵列平台的分子诊断测试开辟了新的可能性。