Three DNA aptamers against HCV core protein were selected: AptHCV14F, AptHCV4.2F and AptHCV7.2R.
•AptHCV14F aptamer is identical to the previously reported AptD-1312 aptamer obtained using different SELEX procedures in another laboratory.
•This aptamer resulted in a high affinity binder of HCV core protein suitable for the development of new generation tools for hepatitis c virus detection and screening.
AbstractHerein, we demonstrate the accuracy of aptamer selection among different SELEX procedures, in different labs, using different variations of the same target and slightly different aptamer initial libraries. In our lab, we have selected DNA aptamers against HCV core protein by applying two consecutive selection approaches (in which two different variations of the target were used): using lysates of E. coli M15 bacteria expressing full-length HCV core protein (genotype 1a) as well as mature HCV core recombinant protein (genotype 1b). Three aptamers were finally identified: AptHCV14F, AptHCV4.2F and AptHCV7.2R, from which AptHCV14F resulted to be identical (within the variable region) to the previously reported (in this journal) aptamer AptD-1312. Functionality of these aptamers were deeply investigated by SPR and ELONA, resulting as high affinity binders of HCV core protein suitable for the development of new generation tools for hepatitis c virus detection and screening.
Graphical abstractaptamers
enzyme-linked oligonucleotide assay
core protein and Hepatitis C Virus
© 2025 The Author(s). Published by Elsevier Ltd.
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