2022
DOI: 10.1016/j.biotechadv.2021.107902
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Strategies to manipulate the performance of aptamers in SELEX, post-SELEX and microenvironment

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Cited by 90 publications
(37 citation statements)
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“…The electrostatic complementarity occurs because of an interaction between the positive and negative charges present on the surfaces of the aptamer and the target. Apart from the electrostatic interaction, other intermolecular interactions such as van der Waals forces, hydrogen bonds and π-π stacking make the aptamer–target complex stable [ 25 ]. They feature distinct characteristics such as compact size, low cost, high specificity, facile chemical modification, and most importantly extraordinary flexibility.…”
Section: Label and Label-free Aptasensorsmentioning
confidence: 99%
“…The electrostatic complementarity occurs because of an interaction between the positive and negative charges present on the surfaces of the aptamer and the target. Apart from the electrostatic interaction, other intermolecular interactions such as van der Waals forces, hydrogen bonds and π-π stacking make the aptamer–target complex stable [ 25 ]. They feature distinct characteristics such as compact size, low cost, high specificity, facile chemical modification, and most importantly extraordinary flexibility.…”
Section: Label and Label-free Aptasensorsmentioning
confidence: 99%
“…MD simulations generate a conformational ensemble of nucleic acid structures at equilibrium and provide detailed atomic motions that aid in understanding structure–function relationships in an aptamer [ 112 , 114 ]. Due to the advantages of incorporating MD simulations into a computational pipeline, an increasing number of published studies report the use of software packages such as NAMD, AMBER, and GROMACS [ 101 , 115 , 116 ]. Ultimately, computational methods could be applied to predict the interactions between an aptamer and its ligand and, hence, refine the nucleic acid sequence to improve the binding affinity and specificity, in addition to being applied for the de novo selection of aptamer in silico [ 114 , 116 ].…”
Section: Nucleic Acid Aptamersmentioning
confidence: 99%
“…Due to the advantages of incorporating MD simulations into a computational pipeline, an increasing number of published studies report the use of software packages such as NAMD, AMBER, and GROMACS [ 101 , 115 , 116 ]. Ultimately, computational methods could be applied to predict the interactions between an aptamer and its ligand and, hence, refine the nucleic acid sequence to improve the binding affinity and specificity, in addition to being applied for the de novo selection of aptamer in silico [ 114 , 116 ]. An overview of the workflow followed for the simulation-based prediction of an aptamer’s interactions with, and affinity for, its ligand is shown in Figure 2 .…”
Section: Nucleic Acid Aptamersmentioning
confidence: 99%
“…This interaction between the aptamer recognition element and the reporter is guided by the way they are written into the DNA blueprint of the biosensor (Fowler & Li, 2014). Moreover, benefiting from the target versatility of aptamer, riboswitch, as the gene structure of reporter protein, can achieve the purpose of highly sensitive and specific detection from small organic molecules to heavy metals, proteins, cells, and even complete virus particles (Oueslati et al., 2018; Qi et al., 2022; Stepanova et al., 2017; Sun et al., 2022). Due to the extremely complex environment of living bacterial cells, target diversity represented the detection of each target with its unique challenges (Hoetzel & Suess, 2022).…”
Section: Introductionmentioning
confidence: 99%