Zoega Morten, Trier Nicole Hartwig, Nejrup Rikke Guldhammer, Chailyan Anna, Friis Tina, Højrup Peter, Houen Gunnar
Department of Autoimmunology and Biomarkers, Statens Serum Institut, DK-2300 Copenhagen S, Denmark.
Department of Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230 Odense M, Denmark.
Antibodies (Basel). 2023 Mar 13;12(1):23. doi: 10.3390/antib12010023.
Proteinase 3 (PR3) is a neutrophil granulocyte enzyme and an autoantigen found in several forms of vasculitis. Due to the diagnostic and clinical importance of antibodies (Abs) to PR3, it is important to characterize the protein and the nature of its epitopes. Here, we have characterized PR3 monoclonal antibodies (MAbs) and disease-associated Abs and their dependency on the PR3 structure and modifications, especially interactions with α-defensins. Three MAbs (HYB 172-01, 172-04, 172-05), which bind to PR3 in its native and denatured forms and provide the disulphide bridges, were intact. α-1-antitrypsin (AT) binds to purified human neutrophil granulocyte PR3 and inhibits its proteolytic activity, towards a small synthetic peptide substrate and a large protein substrate (casein). AT also inhibited the binding of the three MAbs to PR3, indicating that they bind in a region affected by AT binding. However, the MAbs did not inhibit PR3 proteolytic activity with a small substrate, showing that they bound at the active site without restricting access to the substrate cleft. Patient-derived Abs showed essentially the same characteristics as the MAbs, with important implications for vasculitis diagnostics and pathophysiology. Current findings illustrate that PR3 epitopes depend on the three-dimensional structure of the PR3/defensin complex, and that the epitopes depend to a smaller or larger degree on PR3/defensin associations.
蛋白酶3(PR3)是一种中性粒细胞酶,也是在多种血管炎中发现的自身抗原。由于抗PR3抗体(Abs)在诊断和临床方面的重要性,表征该蛋白及其表位的性质很重要。在此,我们表征了PR3单克隆抗体(MAbs)和疾病相关抗体及其对PR3结构和修饰的依赖性,特别是与α-防御素的相互作用。三种能与天然和变性形式的PR3结合并提供二硫键的单克隆抗体(HYB 172-01、172-04、172-05)保持完整。α-1-抗胰蛋白酶(AT)与纯化的人中性粒细胞PR3结合,并抑制其对小合成肽底物和大蛋白质底物(酪蛋白)的蛋白水解活性。AT还抑制了这三种单克隆抗体与PR3的结合,表明它们在受AT结合影响的区域结合。然而,这些单克隆抗体并未抑制PR3对小底物的蛋白水解活性,表明它们在活性位点结合而不限制底物裂隙的可及性。患者来源的抗体表现出与单克隆抗体基本相同的特征,这对血管炎的诊断和病理生理学具有重要意义。目前的研究结果表明,PR3表位取决于PR3/防御素复合物的三维结构,并且这些表位在不同程度上依赖于PR3/防御素的结合。