Recombinant Protein Production Core (rPPC), Chemistry of Life Processes Institute, Northwestern University, Evanston, Illinois, USA.
Department of Integrative Biomedical Sciences, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.
Protein Sci. 2021 Aug;30(8):1577-1593. doi: 10.1002/pro.4091. Epub 2021 May 11.
Angiotensin I-converting enzyme (ACE, CD143) plays a crucial role in blood pressure regulation, vascular remodeling, and immunity. A wide spectrum of mAbs to different epitopes on the N and C domains of human ACE have been generated and used to study different aspects of ACE biology, including establishing a novel approach-conformational fingerprinting. Here we characterized a novel set of 14 mAbs, developed against human seminal fluid ACE. The epitopes for these novel mAbs were defined using recombinant ACE constructs with truncated N and C domains, species cross-reactivity, ACE mutagenesis, and competition with the previously mapped anti-ACE mAbs. Nine mAbs recognized regions on the N domain, and 5 mAbs-on the C domain of ACE. The epitopes for most of these novel mAbs partially overlap with epitopes mapped onto ACE by the previously generated mAbs, whereas mAb 8H1 recognized yet unmapped region on the C domain where three ACE mutations associated with Alzheimer's disease are localized and is a marker for ACE mutation T877M. mAb 2H4 could be considered as a specific marker for ACE in dendritic cells. This novel set of mAbs can identify even subtle changes in human ACE conformation caused by tissue-specific glycosylation of ACE or mutations, and can detect human somatic and testicular ACE in biological fluids and tissues. Furthermore, the high reactivity of these novel mAbs provides an opportunity to study changes in the pattern of ACE expression or glycosylation in different tissues, cells, and diseases, such as sarcoidosis and Alzheimer's disease.
血管紧张素转换酶 (ACE,CD143) 在血压调节、血管重塑和免疫中发挥着关键作用。已经产生了针对人 ACE N 和 C 结构域上不同表位的广泛的单克隆抗体 (mAbs),用于研究 ACE 生物学的不同方面,包括建立新的构象指纹分析方法。在这里,我们描述了一组针对人精液 ACE 开发的 14 种新型 mAbs。这些新型 mAbs 的表位使用具有截断的 N 和 C 结构域的重组 ACE 构建体、种属交叉反应性、ACE 突变和与先前映射的抗 ACE mAbs 的竞争来定义。9 种 mAbs 识别 ACE N 结构域上的区域,而 5 种 mAbs 识别 ACE C 结构域上的区域。这些新型 mAbs 的表位大部分与先前生成的 mAbs 映射到 ACE 上的表位重叠,而 mAb 8H1 识别的是 C 结构域上尚未映射到的区域,其中三个与阿尔茨海默病相关的 ACE 突变定位在此处,并且是 ACE 突变 T877M 的标志物。mAb 2H4 可以被认为是树突状细胞中 ACE 的特异性标志物。这组新型 mAbs 可以识别由于 ACE 的组织特异性糖基化或突变引起的 ACE 构象的甚至细微变化,并可以在生物液和组织中检测人源体细胞和睾丸 ACE。此外,这些新型 mAbs 的高反应性为研究不同组织、细胞和疾病(如结节病和阿尔茨海默病)中 ACE 表达或糖基化模式的变化提供了机会。