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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Establishment of N-succinimidyl 4-(maleimidomethyl) cyclohexanecarboxylate (SMCC) modified biochip enabling concurrent detection of serum infectious antibodies in neuroborreliosis
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Establishment of N-succinimidyl 4-(maleimidomethyl) cyclohexanecarboxylate (SMCC) modified biochip enabling concurrent detection of serum infectious antibodies in neuroborreliosis

机译:N-琥珀酰亚胺基4-(马来酰亚胺基甲基)环己烷羧酸酯(SMCC)修饰的生物芯片的建立,可同时检测神经硼蛋白增生症中的血清感染性抗体

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摘要

In this study, we developed a novel protein biochip that was modified with N-succinimidyl 4-(maleimidomethyl)cyclohexanecarboxylate (SMCC) and specialized for concurrent detection of serum IgG and 1gM antibodies against Borrelia burgdorferi antigens, flagellin, outer surface protein C (OspC) and variable major protein-like sequence (VIsE) in the patients with neuroborreliosis (NB), respectively. Surface chemical characteristics of the biochips were validated with atomic force microscope (AFM) and attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR). The visualized detection limit for IgG antibodies against flagellin, OspC and VIsE antigens on the biochip were 0.78 mu g/ml, 0.78, mu g/ml and 1.56 mu g/ml, respectively. Finally, serum IgG and IgM antibodies in 72 patients with NB and 188 healthy individuals were tested on the biochip. The seroimmunological outcome by the biochip were evaluated in comparison with enzyme linked immunosorbent assay (ELISA) assay. The results demonstrated that the prevalences of IgG and IgM antibodies in the cases were 41.7%, 63.9% to flagellin; 20.8% and 51.4% to OspC and 76.4%, 62.5% to VIsE, respectively. Utilization of the biochip in detection IgM antibody against flagellin was compatible with ELISA assay (R-2=0.849). Thus, the protein biochip would provide a potential platform not only for enabling detection of corresponding antibodies directed against B. burgdorferi antigens, but also for monitoring course of the disease. (C) 2015 Elsevier B.V. All rights reserved.
机译:在这项研究中,我们开发了一种新型蛋白质生物芯片,该生物芯片经过N-琥珀酰亚胺基4-(马来酰亚胺基甲基)环己烷羧酸酯(SMCC)修饰,专门用于同时检测抗伯氏疏螺旋体抗原,鞭毛蛋白,外表面蛋白C(OspC)的血清IgG和1gM抗体。 )和神经硼蛋白缺乏症(NB)患者的可变主要蛋白样序列(VIsE)。生物芯片的表面化学特性已通过原子力显微镜(AFM)和衰减全反射傅里叶变换红外光谱(ATR-FTIR)进行了验证。生物芯片上针对鞭毛蛋白,OspC和VIsE抗原的IgG抗体的可视化检测极限分别为0.78μg / ml,0.78,μg / ml和1.56μg/ ml。最后,在生物芯片上测试了72名NB患者和188名健康个体的血清IgG和IgM抗体。通过生物芯片的血清免疫学结果与酶联免疫吸附试验(ELISA)进行了比较。结果表明,该病例中IgG和IgM抗体的发生率分别为鞭毛蛋白的41.7%,63.9%。 OspC分别为20.8%和51.4%,VIsE分别为76.4%,62.5%。生物芯片在检测抗鞭毛蛋白的IgM抗体中的应用与ELISA分析兼容(R-2 = 0.849)。因此,蛋白质生物芯片将不仅提供可能的平台,用于检测针对伯氏疏螺旋体抗原的相应抗体,而且还可以监测疾病的进程。 (C)2015 Elsevier B.V.保留所有权利。

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