2022
DOI: 10.1016/j.ab.2022.114633
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DNA aptamer selection for SARS-CoV-2 spike glycoprotein detection

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Cited by 15 publications
(11 citation statements)
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References 74 publications
(84 reference statements)
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“…Since the onset of the COVID‐19 pandemic, many aptamers that recognize protein biomarkers from SARS‐CoV‐2 have been reported, [19–40] most of which target the spike protein (S‐protein) of the virus for binding largely because the S‐protein is on the surface of viral particles (and thus is easily accessible) and plays essential roles in virus fusion into host cells [41,42] . These aptamers were isolated using different selection methods (beads‐, filtration‐ or electrophoresis‐based SELEX) and various forms of S‐proteins as binding targets (receptor‐binding domain (RBD), subunit S1, trimeric S‐protein, pseudovirus with S‐protein expressed) [43] .…”
Section: Introductionmentioning
confidence: 99%
“…Since the onset of the COVID‐19 pandemic, many aptamers that recognize protein biomarkers from SARS‐CoV‐2 have been reported, [19–40] most of which target the spike protein (S‐protein) of the virus for binding largely because the S‐protein is on the surface of viral particles (and thus is easily accessible) and plays essential roles in virus fusion into host cells [41,42] . These aptamers were isolated using different selection methods (beads‐, filtration‐ or electrophoresis‐based SELEX) and various forms of S‐proteins as binding targets (receptor‐binding domain (RBD), subunit S1, trimeric S‐protein, pseudovirus with S‐protein expressed) [43] .…”
Section: Introductionmentioning
confidence: 99%
“…Today, research groups have developed different electrode set ups and detection schemes, as well as expanded the menu of analytes, which now includes small molecule drugs (cocaine, 104 ampicilin 105 ), proteins (CRP, 106 insulin 107 ), and viruses (zika virus, 108 avian flu, 109 SARS-CoV-2 (ref. 59 and 110–116)).…”
Section: In Vitro Applicationsmentioning
confidence: 97%
“…efficiency 85%-89%). In order to develop a highthroughput detection method for SARS-CoV-2, two noncompeting aptamers (C7 and C9) against the S protein were isolated by ideal-filter capillary electrophoresis SELEX by Alvarez-Salas et al [32] (Table 1). As the S protein recognition elements, C7 and C9 were used to develop electrochemical sensors and a fluorophore-linked aptamer assay test for SARS-CoV-2.…”
Section: Cov-2 S Proteinmentioning
confidence: 99%
“…Moreover, A1C1 inhibited the interaction between S protein and ACE2 (blocking efficiency 85%–89%). In order to develop a high‐throughput detection method for SARS‐CoV‐2, two noncompeting aptamers (C7 and C9) against the S protein were isolated by ideal‐filter capillary electrophoresis SELEX by Alvarez‐Salas et al [32] . (Table 1).…”
Section: Aptamers Developed For Sars‐cov‐2mentioning
confidence: 99%