NMI, Natural and Medical Sciences Institute, University of Tuebingen, Markwiesenstrasse 55, 72770 Reutlingen, Germany.
Anal Bioanal Chem. 2010 Aug;397(8):3329-38. doi: 10.1007/s00216-010-3873-7. Epub 2010 Jul 18.
Within the last decade, protein microarray technology has been successfully used for the simultaneous quantification of target proteins from minimal amounts of samples in basic and applied proteome research. The robustness and appropriate sensitivity of these miniaturized assays have been demonstrated and thus the transfer to routine and high-throughput applications is now possible. In this study, multiplexed bead-based sandwich immunoassays were used to determine the concentrations of 54 protein analytes, including HER 2 and the estrogen receptor, from ultrasound-guided large-core needle biopsies (LCNBs) from breast cancer patients. Expression levels for HER 2, estrogen receptors and progesterone receptors were also assessed by immunohistochemical routine staining, performed in the clinic on corresponding biopsy samples. The high concordance of the data sets generated with the bead-based protein arrays and by conventional immunohistochemical assessment of HER 2 and the estrogen receptor expressed by breast cancer cells present in the biopsies was demonstrated.
在过去的十年中,蛋白质微阵列技术已成功用于基础和应用蛋白质组学研究中,从少量样本中同时定量测定目标蛋白。这些小型化检测方法的稳健性和适当的灵敏度已得到证明,因此现在可以将其转移到常规和高通量应用中。在这项研究中,使用多重基于珠的夹心免疫测定法来确定 54 种蛋白质分析物的浓度,包括乳腺癌患者超声引导的大芯针活检(LCNB)中的 HER 2 和雌激素受体。还通过免疫组织化学常规染色评估了 HER 2、雌激素受体和孕激素受体的表达水平,该染色在临床中在相应的活检样本上进行。证明了基于珠的蛋白质阵列和通过常规免疫组织化学评估活检中乳腺癌细胞表达的 HER 2 和雌激素受体产生的数据集之间具有高度一致性。