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筛选对单钠尿酸盐和焦磷酸钙二水合物晶体具有特异性结合活性的 Fv 抗体,用于痛风和假性痛风的诊断。

Screening of Fv Antibodies with Specific Binding Activities to Monosodium Urate and Calcium Pyrophosphate Dihydrate Crystals for the Diagnosis of Gout and Pseudogout.

机构信息

Department of Materials Science and Engineering, Yonsei University, 50 Yonsei-Ro, Seodaemun-gu, Seoul 03722, Korea.

Division of Life Sciences, College of Life Science and Bioengineering, Incheon National University, Incheon 22012, Korea.

出版信息

ACS Appl Bio Mater. 2021 Apr 19;4(4):3388-3397. doi: 10.1021/acsabm.0c01680. Epub 2021 Apr 6.

Abstract

To date, medical diagnosis of gout and pseudogout has been performed by observing the crystals in the joint fluid of patients under a polarized microscope. Conventional diagnostic methods using a polarized microscope have disadvantages, such as time-consuming analysis, a high false negative rate, and difficulty in distinguishing gout with monosodium urate (MSU) crystals and pseudogout with calcium pyrophosphate dihydrate (CPPD) crystals in synovial fluids. In this study, a chromogenic assay for the diagnosis of gout and pseudogout, without the requirement of a polarized microscope and trained experts, was proposed using Fv antibodies with specific binding activities to MSU and CPPD crystals. The IgG V chain Fv library with randomized complementarity-determining region 3 (CDR3) region was expressed on the outer membrane of using autodisplay technology. The target Fv antibodies with binding activity to MSU and CPPD crystals were screened from the autodisplayed Fv library on the outer membrane, and five clones were selected. On the basis of the binding properties of the screened Fv antibodies, peptides with the selected clone of amino acid sequences of the CDR3 region (15 residues) were chemically synthesized. The binding properties of the synthetic peptides with amino acid sequences of CDR3 regions from the selected clones were analyzed using fluorescence imaging and flow cytometry, and the affinity constants () of each peptide for binding to MSU and CPPD crystals were calculated by fitting based on the isotherm model. A chromogenic assay configuration for gout and pseudogout was developed using synthetic peptides. In this chromogenic assay, synthetic peptides labeled with biotin and streptavidin-horseradish peroxidase (HRP) complex were used, and crystal detection was possible using a chromogenic reaction between HRP and a chromogenic substrate (TMB). Finally, gout and pseudogout were diagnosed by detecting MSU and CPPD crystals in the synovial fluid in the concentration range of 0-300 μg/mL.

摘要

迄今为止,痛风和假性痛风的医学诊断是通过在偏光显微镜下观察患者关节液中的晶体来进行的。传统的偏光显微镜诊断方法存在分析时间长、假阴性率高以及难以区分关节液中尿酸单钠盐 (MSU) 晶体和焦磷酸钙二水合物 (CPPD) 晶体的缺点。在这项研究中,提出了一种无需偏光显微镜和专业专家即可进行诊断的痛风和假性痛风显色检测方法,该方法使用对 MSU 和 CPPD 晶体具有特异性结合活性的 Fv 抗体。使用自动展示技术在外膜上表达了具有随机互补决定区 3 (CDR3) 区的 IgG V 链 Fv 文库。从自动展示的 Fv 文库中筛选出对 MSU 和 CPPD 晶体具有结合活性的目标 Fv 抗体,并选择了 5 个克隆。基于筛选出的 Fv 抗体的结合特性,用选定的 CDR3 区域(15 个残基)氨基酸序列的克隆合成了具有肽。使用荧光成像和流式细胞术分析了具有选定克隆 CDR3 区域氨基酸序列的合成肽的结合特性,并根据等温模型拟合计算了每个肽与 MSU 和 CPPD 晶体结合的亲和力常数 (Kd)。使用合成肽开发了痛风和假性痛风的显色检测方法。在该显色检测方法中,使用了用生物素和链霉亲和素辣根过氧化物酶 (HRP) 复合物标记的合成肽,并且可以通过 HRP 与显色底物 (TMB) 之间的显色反应检测晶体。最后,通过在 0-300 μg/mL 的浓度范围内检测关节液中的 MSU 和 CPPD 晶体来诊断痛风和假性痛风。

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