Mango-III aptamer(YO3)

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Timeline

The Mango aptamer which can be used to simultaneously fluorescently label and purify biologically important RNAs was selected[1]

An RNA aptamer-based FRET system using single-stranded RNA origami scaffolds was developed[2]

The cocrystal structures of YO3-biotin and Mango III were analyzed to measure the angular dependence of FRET[3]

The characterization of the Mango-III aptamer in complex with the YO3-Biotin fluorophore was described[4]

Description

In 2014, Elena V. Dolgosheina et al. employed in vitro selection techniques to isolate Mango aptamers with high-affinity binding sites for TO1-biotin. Subsequently, they used this motif to design ribozymes displaying polynucleotide kinase activity. In 2021, SUNNY C.Y.JENG et al. elucidated the structure of the Mango-III fluorescent aptamer bound to YO3-Biotin by X-ray diffraction[1,3].


SELEX

This work generated aptamers that bind TO1-biotin using SELEX. An RNA library containing ∼3×1013 random library members was used and TO1-Biotin was conjugated to streptavidin magnetic as positive target. After 12 rounds of SELEX, one RNA family that exhibited both tight binding and a high fluorescent enhancement was identified from 7 distinct families[1].
Detailed information are accessible on SELEX page.



Structure

2D representation

Here we used ribodraw to complete the figure, through the 3D structure information[1].

5'-GCUACGAAGGAAGGAUUGGUAUGUGGUAUAUUCGUAGC-3'

drawing

3D visualisation

In 2021, Sunny C.Y. Jeng et al. analyzed the structure of the Mango-YO3-biotin complexs through crystallization and X-ray diffraction data collection. Coordinates and structure factors have been deposited to the Protein Database under accession codes PDB: 6UP0[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)      

drawing PDBe Molstar





Binding pocket

Left: Surface representation of the binding pocket of the aptamer generated from PDB ID: 1Q8N by X-ray crystallography. YO3-biotin (Oxazole yellow 3-biotin) (shown in sticks) is labeled in yellow. Right: The hydrogen bonds of binding sites of the aptamer bound with YO3-biotin or other nucleotides surround small molecules.

drawing drawing


Ligand information

SELEX ligand

YO3-biotin-RNA aptamer: The EC50 was determined by and measuring the increase in fluorescence as a function of increasing RNA aptamer concentration in the presence of a fixed concentration of dye[2].
TO3-biotin-RNA aptamer: The Kd was determined by and measuring the increase in fluorescence as a function of increasing RNA aptamer concentration in the presence of a fixed concentration of dye[1].


drawing

Structure ligand

YO3 (Oxazole yellow 3) is a synthetic fluorescent small molecule whose spectral properties are very similar to Texas Red. YO3-biotin fluoresces with comparable intensities when bound in either the Mango or the Spinach construct, similarly to TO1-biotin. DFHBI-1T outcompetes YO3-biotin bound in Spinach, whereas YO3-biotin is unable to outcompete DFHBI-1T bound in Spinach.-----Ikeda, S., Kubota, T., Yuki, M., & Okamoto, A. (2009). Exciton‐controlled hybridization‐sensitive fluorescent probes: multicolor detection of nucleic acids. Angewandte Chemie, 121(35), 6602-6606.

PubChem CID Molecular Formula MW CAS Solubility Drugbank ID
59853378 C21H19N2O+ 315.4 g/mol NA NA NA
drawing drawing

Similar compound

We screened the compounds with great similarity to YO3 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
ZINC114784389 2-[(2Z)-2-[(E)-3-(1-methylquinolin-1-ium-4-yl)prop-2-enylidene]-1,3-benzothiazol-3-yl]acetic acid NA 59274362 drawing


References

[1] RNA mango aptamer-fluorophore: a bright, high-affinity complex for RNA labeling and tracking.
Dolgosheina, E. V., Jeng, S. C., Panchapakesan, S. S., Cojocaru, R., Chen, P. S., Wilson, P. D., Hawkins, N., Wiggins, P. A., & Unrau, P. J.
ACS chemical biology, 9(10), 2412–2420. (2014)
[2] Development of a genetically encodable FRET system using fluorescent RNA aptamers.
Jepsen, M. D. E., Sparvath, S. M., Nielsen, T. B., Langvad, A. H., Grossi, G., Gothelf, K. V., & Andersen, E. S.
Nature communications, 9(1), 18. (2018)
[3] Fluorogenic aptamers resolve the flexibility of RNA junctions using orientation-dependent FRET.
Jeng, S. C. Y., Trachman, R. J., 3rd, Weissenboeck, F., Truong, L., Link, K. A., Jepsen, M. D. E., Knutson, J. R., Andersen, E. S., Ferré-D'Amaré, A. R., & Unrau, P. J.
RNA (New York, N.Y.), 27(4), 433–444. (2021)
[4] Characterizing fluorescence properties of turn-on RNA aptamers.
Trachman, R. J., 3rd, Link, K. A., Knutson, J. R., & Ferré-D'Amaré, A. R.
Methods in molecular biology (Clifton, N.J.), 2568, 25–36. (2023)