2019
DOI: 10.1007/s00216-019-02219-w
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A novel zinc finger protein–based amperometric biosensor for miRNA determination

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Cited by 26 publications
(5 citation statements)
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“…One of the strategies to overcome the miR-21 short length issue is using zinc finger proteins (ZFPs). 31 A zinc finger is a small peptide with a specific secondary structure that is stabilized via the binding of zinc ions with histidines and two cysteines to bind miRNAs. 32 Povedano et al 31 designed a biosensor based on ZFP biorecognition for capturing the RNA hybrid formed between miR-21 molecules and achieved a LOD of 0.91 nM.…”
Section: Bioanalytical Systemsmentioning
confidence: 99%
See 1 more Smart Citation
“…One of the strategies to overcome the miR-21 short length issue is using zinc finger proteins (ZFPs). 31 A zinc finger is a small peptide with a specific secondary structure that is stabilized via the binding of zinc ions with histidines and two cysteines to bind miRNAs. 32 Povedano et al 31 designed a biosensor based on ZFP biorecognition for capturing the RNA hybrid formed between miR-21 molecules and achieved a LOD of 0.91 nM.…”
Section: Bioanalytical Systemsmentioning
confidence: 99%
“…31 A zinc finger is a small peptide with a specific secondary structure that is stabilized via the binding of zinc ions with histidines and two cysteines to bind miRNAs. 32 Povedano et al 31 designed a biosensor based on ZFP biorecognition for capturing the RNA hybrid formed between miR-21 molecules and achieved a LOD of 0.91 nM. Hybridization chain reaction (HCR), strand displacement amplification (SDA), loop-mediated isothermal amplification (LAMP), rolling circle amplification (RCA), and target-catalyzed hairpin assembly (CHA) are some isothermal nucleic acid amplification techniques developed for miRNA detection.…”
Section: Bioanalytical Systemsmentioning
confidence: 99%
“…The linear range was 4-50 fM with a linear regression equation of I (µA) = −9.81 logc (fM) + 4.26 (R 2 = 0.992), and the LOD was down to 120 aM (S/N = 3). The detection performance was comparable to and even better than most reported nanomaterials-based electrochemical assays for miRNA detection (Table 2) [26,[33][34][35][36][37] but without sophisticated electrode modifications. The high sensitivity of this method can be attributed to the three amplification strategies, including magnetic enrichment, enzymatic polymerization, and the use of Cu 2+ ions in SWV.…”
Section: Calibration Curves For Mirnas Detectionmentioning
confidence: 60%
“…This happens because the interactivity exhibited by the hexahistidine tag (H6) and other His-rich tails with Ni 2+ during the immobilized metal affinity chromatographic (IMAC) purification of recombinant proteins [2,3] can be also exploited for a controlled crossmolecular assembly, when adding defined amounts of Zn 2+ , Ca 2+ , Mn 2+ or other divalent cations to solutions of pure Histagged protein [4][5][6]. In fact, this principle sustains the formation of the secretory granules in the mammalian endocrine system [7,8] and of different types of amyloidal and non-amyloidal protein materials existing in nature [4,7,[9][10][11][12][13][14][15][16]. The simplicity of His-rich peptides used as architectonic agents at the nanoscale offers an interesting alternative to more refined approaches to control protein self-assembling, that might require more sophisticated protein engineering [17][18][19][20][21].…”
Section: Introductionmentioning
confidence: 99%