2021
DOI: 10.1016/j.trac.2021.116311
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Mapping the gaps in chemical analysis for the characterisation of aptamer-target interactions

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Cited by 42 publications
(46 citation statements)
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References 146 publications
(181 reference statements)
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“…Labels are employed in electrochemical biosensors to boost the signal produced per occurrence. Electrochemical labelling often involves chemical methods that covalently bind labels, but some probe labelling merely requires momentary (physical-binding) attachments [ 75 , 76 , 77 ]. In one of the fascinating studies, Karash et al designed an impedance-based aptasensor utilizing a specific avian influenza virus (AIV) H5N1 aptamer and a gold interdigitated microelectrode.…”
Section: Label and Label-free Aptasensorsmentioning
confidence: 99%
“…Labels are employed in electrochemical biosensors to boost the signal produced per occurrence. Electrochemical labelling often involves chemical methods that covalently bind labels, but some probe labelling merely requires momentary (physical-binding) attachments [ 75 , 76 , 77 ]. In one of the fascinating studies, Karash et al designed an impedance-based aptasensor utilizing a specific avian influenza virus (AIV) H5N1 aptamer and a gold interdigitated microelectrode.…”
Section: Label and Label-free Aptasensorsmentioning
confidence: 99%
“…The study of the binding kinetics and thermodynamics, along with the structural features of the peptidetarget complex, is instrumental in evaluating the applicability of the selected peptide as a bioreceptor and, eventually, the identification of the most suitable design for the sensing platform. The design of the peptide-target characterisation protocol should take into account the final application of the peptide sequence (i.e., the biosensing platform) as the binding performance can vary depending on the physical and chemical properties of the surrounding environment, as recently discussed for other biorecognition elements [32]. Characterisation of the peptide-target complex is therefore fundamental to the evaluation of the peptide's applicability, the discrimination of a restricted pool of selected sequences, and, eventually, the consideration to improve biorecognition elements, for instance, by using peptides in conjugation with other biomolecules [33,34].…”
Section: Peptide Selection Synthesis and Characterisationmentioning
confidence: 99%
“…The interaction between an aptamer and its target is the core of the SELEX process and practical application. The nature of this interaction depends on the type and size of the target [143]. When the target is a small molecule, the aptamer can integrate the target into its structure through stacking (with flat, aromatic ligands and ions), electrostatic complementation (with oligosaccharides and charged amino acids), and/or hydrogen bonding interactions [144].…”
Section: Aptamer-target Interaction Mechanismsmentioning
confidence: 99%