DNA aptamer selection for SARS-CoV-2 spike glycoprotein detection

被引:16
|
作者
Alejandro Martinez-Roque, Mateo [1 ]
Alberto Franco-Urquijo, Pablo [1 ]
Miguel Garcia-Velasquez, Victor [1 ]
Choukeife, Moujab [2 ]
Mayer, Guenther [2 ]
Molina-Ramirez, Sergio Roberto [3 ]
Figueroa-Miranda, Gabriela [3 ]
Mayer, Dirk [3 ]
Alvarez-Salas, Luis M. [1 ]
机构
[1] IPN, Ctr Invest & Estudios Avanzados, Dept Genet & Biol Mol, Lab Terapia Gen, Cdmx 07360, Mexico
[2] Univ Bonn, Life & Med Sci LIMES Inst, D-53121 Bonn, Germany
[3] Forschungszentrum Julich, Inst Biol Informat Proc Bioelect IBI 3, D-52428 Julich, Germany
关键词
Aptamers; SELEX; SARS-CoV-2; COVID-19; Aptasensor; Capillary electrophoresis; IN-VITRO SELECTION; ELECTROPHORESIS-SELEX SELECTION; CAPILLARY-ELECTROPHORESIS; AFFINITY; CORONAVIRUS; EVOLUTION; DISCOVERY; PROTEINS; LIGANDS;
D O I
10.1016/j.ab.2022.114633
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The rapid spread of SARS-CoV-2 infection throughout the world led to a global public health and economic crisis triggering an urgent need for the development of low-cost vaccines, therapies and high-throughput detection assays. In this work, we used a combination of Ideal-Filter Capillary Electrophoresis SELEX (IFCE-SELEX), Next Generation Sequencing (NGS) and binding assays to isolate and validate single-stranded DNA aptamers that can specifically recognize the SARS-CoV-2 Spike glycoprotein. Two selected non-competing DNA aptamers, C7 and C9 were successfully used as sensitive and specific biological recognition elements for the development of electrochemical and fluorescent aptasensors for the SARS-CoV-2 Spike glycoprotein with detection limits of 0.07 fM and 41.87 nM, respectively.
引用
收藏
页数:10
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