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一种基于新型肽的严重急性呼吸综合征冠状病毒2抗体检测方法。

A Novel Peptide-Based Detection of SARS-CoV-2 Antibodies.

作者信息

Bulut Aliye, Temur Betul Z, Kirimli Ceyhun E, Gok Ozgul, Balcioglu Bertan K, Ozturk Hasan U, Uyar Neval Y, Kanlidere Zeynep, Kocagoz Tanil, Can Ozge

机构信息

Department of Biomedical Engineering, Institute of Biomedical Engineering, Bogazici University, Istanbul 34684, Turkey.

Department of Medical Biotechnology, Institute of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul 34752, Turkey.

出版信息

Biomimetics (Basel). 2023 Feb 22;8(1):89. doi: 10.3390/biomimetics8010089.

DOI:10.3390/biomimetics8010089
PMID:36975319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10046560/
Abstract

The need for rapidly developed diagnostic tests has gained significant attention after the recent pandemic. Production of neutralizing antibodies for vaccine development or antibodies to be used in diagnostic tests usually require the usage of recombinant proteins representing the infectious agent. However, peptides that can mimic these recombinant proteins may be rapidly utilized, especially in emergencies such as the recent outbreak. Here, we report two peptides that mimic the receptor binding domain of the spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and investigate their binding behavior against the corresponding human immunoglobulin G and immunoglobulin M (IgG and IgM) antibodies in a clinical sample using a quartz crystal microbalance (QCM) sensor. These peptides were immobilized on a QCM sensor surface, and their binding behavior was studied against a clinical serum sample that was previously determined to be IgG and IgM-positive. It was determined that designed peptides bind to SARS-CoV-2 antibodies in a clinical sample. These peptides might be useful for the detection of SARS-CoV-2 antibodies using different methods such as enzyme-linked immunosorbent assay (ELISA) or lateral flow assays. A similar platform might prove to be useful for the detection and development of antibodies in other infections.

摘要

在最近的疫情大流行之后,对快速开发的诊断测试的需求受到了极大关注。用于疫苗开发的中和抗体或用于诊断测试的抗体的生产通常需要使用代表感染因子的重组蛋白。然而,能够模拟这些重组蛋白的肽可能会被迅速利用,尤其是在诸如最近的疫情爆发等紧急情况下。在此,我们报告了两种模拟严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白受体结合域的肽,并使用石英晶体微天平(QCM)传感器研究了它们在临床样本中与相应的人类免疫球蛋白G和免疫球蛋白M(IgG和IgM)抗体的结合行为。这些肽被固定在QCM传感器表面,并针对先前确定为IgG和IgM阳性的临床血清样本研究了它们的结合行为。结果确定,设计的肽在临床样本中与SARS-CoV-2抗体结合。这些肽可能有助于使用酶联免疫吸附测定(ELISA)或侧向流动测定等不同方法检测SARS-CoV-2抗体。类似的平台可能被证明对其他感染中抗体的检测和开发有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/59132c0beedd/biomimetics-08-00089-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/85f1ea47dd02/biomimetics-08-00089-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/f98aa61250ed/biomimetics-08-00089-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/44adce2ead3e/biomimetics-08-00089-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/0fb8cf39e8dd/biomimetics-08-00089-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/13c8032d0276/biomimetics-08-00089-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/8735ddde9de9/biomimetics-08-00089-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/59132c0beedd/biomimetics-08-00089-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/85f1ea47dd02/biomimetics-08-00089-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/f98aa61250ed/biomimetics-08-00089-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/44adce2ead3e/biomimetics-08-00089-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/0fb8cf39e8dd/biomimetics-08-00089-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/13c8032d0276/biomimetics-08-00089-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/8735ddde9de9/biomimetics-08-00089-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2f/10046560/59132c0beedd/biomimetics-08-00089-g007.jpg

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