Tsai H M, Sussman I I, Ginsburg D, Lankhof H, Sixma J J, Nagel R L
Division of Hematology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY 10467, USA.
Blood. 1997 Mar 15;89(6):1954-62.
The susceptibility of recombinant type 2A von Willebrand factor (vWF) to a recently identified plasma metalloproteinase and the potential application of proteolysis inhibition in the treatment of the disease were investigated. Two recombinant type 2A vWF mutants, R834W and R834Q, were spontaneously cleaved by the partially purified plasma proteinase to smaller forms. When treated with guanidine HCI, both the wild-type and the R834W mutant vWF exhibited a biphasic change in proteolytic susceptibility, reaching the same maximum cleavage at 1.25 mol/L guanidine HCI. Proteolysis of the recombinant vWF generated the same 350-kD and 200-kD species (dimers of the 176-kD and 140-kD fragments, respectively) as those found in normal plasma. The proteinase activity was inhibited by doxycycline, with an IC50 of approximately 0.25 mmol/L. The inhibitory activity of doxycycline was related to its metallic cation binding activity. Susceptibility of the recombinant vWF to the proteinase was inhibited by monoclonal antibody VP-1 (directed against residues 828-842 of the vWF polypeptide), but not by two other monoclonal antibodies M13 and M31. The spontaneous susceptibility to proteolytic cleavage may account for the lack of large multimers in type 2A von Willebrand disease (vWD), and the results with tetracyclines and monoclonal antibody VP-1 offer new strategies for developing specific treatment of type 2A vWD.
研究了重组2A型血管性血友病因子(vWF)对最近发现的一种血浆金属蛋白酶的敏感性以及蛋白水解抑制在该疾病治疗中的潜在应用。两种重组2A型vWF突变体R834W和R834Q被部分纯化的血浆蛋白酶自发切割成较小的形式。用盐酸胍处理时,野生型和R834W突变体vWF在蛋白水解敏感性上均呈现双相变化,在1.25 mol/L盐酸胍时达到相同的最大切割程度。重组vWF的蛋白水解产生了与正常血浆中相同的350-kD和200-kD片段(分别为176-kD和140-kD片段的二聚体)。强力霉素可抑制该蛋白酶活性,IC50约为0.25 mmol/L。强力霉素的抑制活性与其金属阳离子结合活性有关。重组vWF对该蛋白酶的敏感性受到单克隆抗体VP-1(针对vWF多肽的828 - 842位残基)的抑制,但未受到另外两种单克隆抗体M13和M31的抑制。蛋白水解切割的自发敏感性可能解释了2A型血管性血友病(vWD)中缺乏大的多聚体的现象,而四环素和单克隆抗体VP-1的研究结果为开发2A型vWD的特异性治疗方法提供了新策略。