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用于区分正常血管性血友病因子和2B型血管性血友病的构象特异性RNA适配体。

Conformation-specific RNA aptamers for phenotypic distinction between normal von Willebrand factor and type 2B von Willebrand disease.

作者信息

Machha Venkata R, Tischer Alexander, Moon-Tasson Laurie, Tange Julie, Santiago-Davis Annyoceli, Pruthi Rajiv K, Chen Dong, Maher L James, Auton Matthew

机构信息

Division of Hematology, Department of Internal Medicine, Mayo Clinic, 200 1st St SW, Rochester, MN, USA.

Department of Biochemistry and Molecular Biology, Mayo Clinic, 200 1st St SW, Rochester, MN 55905, USA.

出版信息

NAR Mol Med. 2024 Nov 23;1(4):ugae021. doi: 10.1093/narmme/ugae021. eCollection 2024 Oct.

Abstract

The A1 domain in Von Willebrand Factor (VWF) initiates coagulation through binding to platelet glycoprotein GPIbα receptors. Von Willebrand Disease (VWD)-Mutations in A1 that either impair (type 2M) or enhance (type 2B) platelet adhesion to VWF can locally destabilize and even misfold the domain. We leveraged misfolding in the gain-of-function type 2B VWD phenotype as a target, distinct from the normal conformation. Two nuclease-resistant 2'-fluoropyrimidine RNA aptamers were selected to discriminate normal A1 domains from a type 2B V1314D A1 variant in a glycosylated A1A2A3 tri-domain VWF-fragment. Two aptamers, W9 and V1, were isolated that selectively recognize, bind, and inhibit the A1-GPIbα interaction with WT A1A2A3 and V1314D A1A2A3, respectively. These aptamers were tested against their respective recombinant targets, plasma VWF, VWF concentrates, and patient plasma with the heterozygous type 2B VWD R1306W variant using clinical assays, surface plasmon resonance and inhibition assays of platelet adhesion to recombinant A1 and A1A2A3 domains under shear stress. The specificity of W9 and V1 aptamers confirms that pathological conformations of VWD Type 2B proteins are different from normal VWF. The availability of aptamers that distinguish normal plasma-derived VWF from VWD suggests potential applicability in clinical diagnosis of severe gain-of-function phenotypes.

摘要

血管性血友病因子(VWF)中的A1结构域通过与血小板糖蛋白GPIbα受体结合来启动凝血过程。血管性血友病(VWD)——A1结构域中的突变,无论是损害(2M型)还是增强(2B型)血小板与VWF的黏附,都可能使该结构域局部不稳定甚至错误折叠。我们利用功能获得型2B型VWD表型中的错误折叠作为靶点,该靶点不同于正常构象。我们选择了两种抗核酸酶的2'-氟嘧啶RNA适配体,以区分糖基化的A1A2A3三结构域VWF片段中的正常A1结构域和2B型V1314D A1变体。分离出了两种适配体W9和V1,它们分别选择性地识别、结合并抑制WT A1A2A3和V1314D A1A2A3的A1-GPIbα相互作用。使用临床检测、表面等离子体共振以及在剪切应力下血小板对重组A1和A1A2A3结构域黏附的抑制检测,针对它们各自的重组靶点、血浆VWF、VWF浓缩物以及携带杂合型2B型VWD R1306W变体的患者血浆对这些适配体进行了测试。W9和V1适配体的特异性证实了2B型VWD蛋白的病理构象与正常VWF不同。能够区分正常血浆来源的VWF和VWD的适配体的可用性表明其在严重功能获得型表型的临床诊断中具有潜在的适用性。

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