DNA aptamer selection for SARS-CoV-2 spike glycoprotein detection. Academic Article uri icon

Overview

abstract

  • 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.

authors

  • Martinez Roque, Mateo
  • Franco-Urquijo, Pablo Alberto
  • García-Velásquez, Víctor Miguel
  • Choukeife, Moujab
  • Mayer, Günther
  • Molina-Ramírez, Sergio Roberto
  • Figueroa-Miranda, Gabriela
  • Mayer, Dirk
  • Alvarez-Salas, Luis M

publication date

  • March 2, 2022

Research

keywords

  • Aptamers, Nucleotide
  • COVID-19

Identity

PubMed Central ID

  • PMC8889740

Scopus Document Identifier

  • 85126042055

Digital Object Identifier (DOI)

  • 10.1016/j.bioelechem.2020.107589

PubMed ID

  • 35247355

Additional Document Info

volume

  • 645