Department Pathology, Institute of Surgical Pathology, University Hospital of Zurich, Zurich, Switzerland.
Mod Pathol. 2010 Sep;23(9):1289-97. doi: 10.1038/modpathol.2010.103. Epub 2010 May 21.
Designed ankyrin repeat proteins are a novel class of specific binding molecules, which display increased thermodynamic stability, smaller size and at least equal target affinity compared to immunoglobulins, making them potentially powerful tools in diagnostic pathology and therapeutic oncology. Here, we investigated whether designed ankyrin repeat proteins can reliably identify the amplification status of the epidermal growth factor receptor 2 in breast cancer. Designed ankyrin repeat proteins specific for epidermal growth factor receptor 2 were tested in paraffin-embedded tissue sections. Detection using enzymatic biotinylation proved to be most specific and sensitive. The affinity of the designed ankyrin repeat proteins was found crucial, but for a picomolar binder no further gain was found by making it multivalent. The best designed ankyrin repeat protein, G3 (K(D) 90 pM) was compared on breast cancer tissue microarrays (n=792) to an FDA-approved rabbit monoclonal antibody against epidermal growth factor receptor 2 (clone 4B5; Ventana Medical Systems) and correlated with corresponding epidermal growth factor receptor 2 amplification status measured by fluorescent in situ hybridization. Amplification status and epidermal growth factor receptor 2 expression measured by designed ankyrin repeat protein and antibody correlated strongly with each other (P<0.0001 each), the correlation between designed ankyrin repeat protein and amplification status being the strongest (0.87 compared to 0.77 for the antibody, Kendall's tau-beta). Using a modified scoring system for the designed ankyrin repeat protein, we show that the designed ankyrin repeat protein detects a positive epidermal growth factor receptor 2 amplification status with similar sensitivity and significantly higher specificity than the antibody (P=0.0005). This study suggests that designed ankyrin repeat proteins provide a valuable alternative to antibodies for the detection of epidermal growth factor receptor 2 expression in breast cancer and adds further compelling evidence for the use of designed ankyrin repeat proteins in diagnostic pathology and therapeutic oncology.
设计的锚蛋白重复蛋白是一类新型的特异性结合分子,与免疫球蛋白相比,它们具有更高的热力学稳定性、更小的尺寸和至少相等的靶亲和力,因此它们可能成为诊断病理学和治疗肿瘤学中的有力工具。在这里,我们研究了设计的锚蛋白重复蛋白是否可以可靠地识别乳腺癌中表皮生长因子受体 2 的扩增状态。针对表皮生长因子受体 2 的设计的锚蛋白重复蛋白在石蜡包埋的组织切片中进行了测试。使用酶促生物素化检测被证明是最特异和敏感的。发现设计的锚蛋白重复蛋白的亲和力至关重要,但对于皮摩尔结合物,通过使其多价化并没有进一步提高亲和力。最佳的设计的锚蛋白重复蛋白 G3(K(D)90pM)在乳腺癌组织微阵列(n=792)上与经 FDA 批准的针对表皮生长因子受体 2 的兔单克隆抗体(克隆 4B5;Ventana Medical Systems)进行了比较,并与通过荧光原位杂交测量的相应表皮生长因子受体 2 扩增状态相关。通过设计的锚蛋白重复蛋白和抗体测量的扩增状态和表皮生长因子受体 2 表达彼此之间强烈相关(均 P<0.0001),设计的锚蛋白重复蛋白与扩增状态的相关性最强(0.87 相比抗体为 0.77,Kendall 的 tau-beta)。使用设计的锚蛋白重复蛋白的改良评分系统,我们表明该蛋白可以检测到表皮生长因子受体 2 的阳性扩增状态,具有相似的敏感性和明显更高的特异性,优于抗体(P=0.0005)。这项研究表明,设计的锚蛋白重复蛋白为检测乳腺癌中的表皮生长因子受体 2 表达提供了抗体的一种有价值的替代方法,并为设计的锚蛋白重复蛋白在诊断病理学和治疗肿瘤学中的应用提供了进一步的有力证据。