Biotin aptamer
Timeline
Biotin-binding RNAs and DNAs (aptamers) isolated by in vitro selection from random sequence pools[1]
Reported a replacement assay for the detection of biotin using a replaceable liposomal aptamer[4]
Description
In 1998, Szostak, J employed in vitro selection techniques to isolate aptamers with affinity binding sites for biotin. In 2000, Nix, J. C. determined the 1.3 Å crystal structure of the aptamer complexed with biotin. Biotin is bound at the interface between the pseudoknot's stacked helices in a pocket defined almost entirely by base-paired nucleotides. The structure provides general insight into the mechanisms by which RNA function is mediated by divalent metals[1,3].SELEX
A randomized RNA library, consisting of approximately 1014 molecules, was synthesized via in vitro transcription from a DNA template and resuspended in a selection buffer comprising 0.1 M KCl, 5 mM MgCl2, and 10 mM Na-HEPES at pH 7.4. Following equilibration at ambient temperature, the RNA pool was applied to a 500 μL biotin-agarose affinity column to selectively bind biotin-interacting RNAs. Non-specific binders were eliminated through a series of 15 washes with 500 μL of the selection buffer. The biotinylated RNAs were eluted using 5 volumes of 500 μL elution buffer, which was the selection buffer supplemented with 5 mM D-biotin at pH 7.4. The affinity-purified RNAs were then pooled, concentrated, and subjected to enzymatic amplification. The resulting enriched RNA pool underwent gel purification and was cycled through additional rounds of selection and amplification. Notably, biotin-binding RNA species were first identified in the fourth selection round, and by the seventh round, these RNAs constituted over 50% of the total sequences present in the pool[1].
Detailed information are accessible on SELEX page.
Structure
2D representation
Here we use ribodraw to complete the figure, through the 3D structure information[3].
5'-GGACCGUCAGAGGACACGGUUAAAAAGUCCUCU-3'
3D visualisation
Nix, J. et al. determined the structure of the biotin RNA aptamer using X-ray crystallography. The aptamer structure reveals how a highly complementary binding pocket for an unusual ligand can be built by an RNA using mostly Watson-Crick base-paired nucleotides and a collection of bound solvent molecules. The PDB ID of this structure is 1F27[3].Additional available structures that have been solved and detailed information are accessible on Structures page.
(Clicking the "Settings/Controls info" to turn Spin off)
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Binding pocket
Left: Surface representation of the binding pocket of the aptamer generated from PDB ID: 1F27 by X-ray crystallography. Biotin (shown in sticks) is labeled in yellow. Right: The hydrogen bonds of binding sites of the aptamer bound with Biotin.Ligand information
SELEX ligand
The affinity of the aptamer for biotin was determined by measuring the fraction of RNA bound to biotin agarose at a range of immobilized ligand concentrations. The concentration of biotin available for binding was determined by saturating biotin agarose with excess labeled aptamer and measuring the amount of RNA specifically eluted following washing[1].Structure ligand
Biotin is one of the vitamin B groups, also known as vitamin H, vitamin B7, coenzyme R (Coenzyme R) and so on. Biotin is abundant in liver, kidney, yeast and milk, and it is an important factor for organisms to fix carbon dioxide. It is easy to combine with protein Avidin in egg white. Eating a large amount of raw protein can hinder the absorption of biotin and lead to biotin deficiency, such as depilation, weight loss and dermatitis. Because its deficiency rarely occurs, it is often called biotin directly.-----From Wiki
Name | PubChem CID | Molecular Formula | MW | CAS | Solubility | Drugbank ID |
---|---|---|---|---|---|---|
Biotin | 171548 | C10H16N2O3S | 244.31 g/mol | 58-85-5 | 220 mg/L (at 25 °C) | DB00121 |
Similar compound
We screened the compounds with great similarity to biotin by using the ZINC database and showed some of the compounds' structure diagrams. For some CAS numbers not available,we will supplement them with Pubchem CID.
Zinc_id | Named | CAS | Pubchem CID | Structure |
---|---|---|---|---|
ZINC4095742 | Biotin Amide | 6929-42-6 | 439597 | |
ZINC3870809 | 2-Iminobiotin | NA | 46936649 | |
ZINC13543600 | Lydimycin | NA | 70685126 | |
ZINC2169827 | vitamin H | NA | 6560210 | |
ZINC4321698 | Biotin Sulfone | 40720-05-6 | 83863 | |
ZINC4096827 | Biocytin | 576-19-2 | 83814 | |
ZINC5192424 | Bisnorbiotin | 16968-98-2 | 86492 | |
ZINC4521221 | Biotin-X | 72040-64-3 | 446905 |
References
[1] Functional requirements for specific ligand recognition by a biotin-binding RNA pseudoknot.Wilson, C., Nix, J., & Szostak, J.
Biochemistry, 37(41), 14410–14419. (1998)
[2] Preliminary crystallographic characterization of an in vitro evolved biotin-binding RNA pseudoknot.
Nix, J. C., Newhoff, A. R., & Wilson, C.
Acta crystallographica. Section D, Biological crystallography, 55(Pt 1), 323–325. (1999)
[3] The 1.3 A crystal structure of a biotin-binding pseudoknot and the basis for RNA molecular recognition.
Nix, J., Sussman, D., & Wilson, C.
Journal of molecular biology, 296(5), 1235–1244. (2000)
[4] A replaceable liposomal aptamer for the ultrasensitive and rapid detection of biotin.
Sung, T. C., Chen, W. Y., Shah, P., & Chen, C. S.
Scientific reports, 6, 21369. (2016)
[5] Pull-down of Biotinylated RNA and Associated Proteins.
Uppala, J. K., Ghosh, C., Sabat, G., & Dey, M.
Bio-protocol, 12(4), e4331. (2022)