Cosandey Vincent, Debrot Fabien, Kaeser Jérémy, Marti Roger, Passeraub Philippe, Pétremand Jannick, Prim Denis, Pfeifer Marc E
HES-SO Valais, Institute of Life Technologies, Route du Rawyl 47, CH-1950 Sion 2, Switzerland.
Chimia (Aarau). 2012;66(10):803-6. doi: 10.2533/chimia.2012.803.
Peptide and protein microarrays provide a multiplex approach to identification and quantification of protein-protein interactions (PPI), useful to study for instance antigen-antibody properties. Multivariate serology assays detecting multiple tumor auto-antibodies (TAA) is an emerging class of blood tests for cancer detection. Here we describe the efficient coupling of peptide baits derived from the BRCA1-associated RING domain protein 1 (BARD1) to a solid surface and detection of a commercially available anti-BARD1 antibody with this newly designed peptide microarray. Analytical sensitivity and specificity were shown to be comparable to a microtiter plate based enzyme-linked immunosorbent assay (ELISA).
肽和蛋白质微阵列提供了一种用于蛋白质-蛋白质相互作用(PPI)鉴定和定量的多重方法,例如在研究抗原-抗体特性方面很有用。检测多种肿瘤自身抗体(TAA)的多变量血清学检测是一类新兴的癌症检测血液检测方法。在此,我们描述了将源自乳腺癌1号基因(BRCA1)相关环指结构域蛋白1(BARD1)的肽诱饵有效偶联到固体表面,并使用这种新设计的肽微阵列检测市售抗BARD1抗体。分析灵敏度和特异性显示与基于微孔板的酶联免疫吸附测定(ELISA)相当。