Selective discrimination and classification of G-quadruplex structures with a host-guest sensing array.


Journal

Nature chemistry
ISSN: 1755-4349
Titre abrégé: Nat Chem
Pays: England
ID NLM: 101499734

Informations de publication

Date de publication:
05 2021
Historique:
received: 14 01 2020
accepted: 27 01 2021
pubmed: 3 4 2021
medline: 3 8 2021
entrez: 2 4 2021
Statut: ppublish

Résumé

The secondary structures of nucleic acids have an important influence on their cellular functions but can be difficult to identify and classify quickly. Here, we show that an arrayed suite of synthetic hosts and dyes is capable of fluorescence detection of oligonucleotide secondary structures. Multivariate analysis of different fluorescence enhancements-generated using cationic dyes that show affinity for both DNA G-quadruplexes and the synthetic hosts-enables discrimination between G-quadruplex structures of identical length and highly similar topological types. Different G-quadruplexes that display the same folding topology can also be easily differentiated by the number of G-quartets and sequence differences at the 3' or 5' ends. The array is capable of both differentiation and classification of the G-quadruplex structures at the same time. This simple non-invasive sensing method does not require the discovery and synthesis of specific G-quadruplex binding ligands, but employs a simple multicomponent approach to ensure wide applicability.

Identifiants

pubmed: 33795843
doi: 10.1038/s41557-021-00647-9
pii: 10.1038/s41557-021-00647-9
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

488-495

Références

Belmont, P., Constant, J.-F. & Demeunynck, M. Nucleic acid conformation diversity: from structure to function and regulation. Chem. Soc. Rev. 30, 70–81 (2001).
doi: 10.1039/a904630e
Balasubramanian, S., Hurley, L. H. & Neidle, S. Targeting G-quadruplexes in gene promoters: a novel anticancer strategy? Nat. Rev. Drug Discovery 10, 261–275 (2011).
pubmed: 21455236 doi: 10.1038/nrd3428
Seeman, N. C. & Sleiman, H. F. DNA nanotechnology. Nat. Rev. Mater. 3, 17068 (2017).
doi: 10.1038/natrevmats.2017.68
Pinheiro, A. V., Han, D., Shih, W. M. & Yan, H. Challenges and opportunities for structural DNA nanotechnology. Nat. Nanotechnol. 6, 763–772 (2011).
pubmed: 22056726 pmcid: 3334823 doi: 10.1038/nnano.2011.187
Jaeger, L. & Chworos, A. The architectonics of programmable RNA and DNA nanostructures. Curr. Opin. Struct. Biol. 16, 531–543 (2006).
pubmed: 16843653 doi: 10.1016/j.sbi.2006.07.001
Winnerdy, F. R. et al. NMR solution and X-ray crystal structures of a DNA containing both right-and left-handed parallel-stranded G-quadruplexes. Nucleic Acids Res. 47, 8272–8281 (2019).
pubmed: 31216034 pmcid: 6735952 doi: 10.1093/nar/gkz349
Salgado, G. F., Cazenave, C., Kerkour, A. & Mergny, J.-L. G-quadruplex DNA and ligand interaction in living cells using NMR spectroscopy. Chem. Sci. 6, 3314–3320 (2015).
pubmed: 28706695 pmcid: 5490339 doi: 10.1039/C4SC03853C
del Villar-Guerra, R., Trent, J. O. & Chaires, J. B. G-quadruplex secondary structure obtained from circular dichroism spectroscopy. Angew. Chem. Int. Ed. 57, 7171–7175 (2018).
doi: 10.1002/anie.201709184
Eubanks, C. S., Forte, J. E., Kapral, G. J. & Hargrove, A. E. Small molecule-based pattern recognition to classify RNA structure. J. Am. Chem. Soc. 139, 409–416 (2017).
pubmed: 28004925 doi: 10.1021/jacs.6b11087
You, L., Zha, D. & Anslyn, E. V. Recent advances in supramolecular analytical chemistry using optical sensing. Chem. Rev. 115, 7840–7892 (2015).
pubmed: 25719867 doi: 10.1021/cr5005524
Eubanks, C. S. et al. Visualizing RNA conformational changes via pattern recognition of RNA by small molecules. J. Am. Chem. Soc. 141, 5692–5698 (2019).
pubmed: 30860826 pmcid: 6639014 doi: 10.1021/jacs.8b09665
Stewart, S., Ivy, M. A. & Anslyn, E. V. The use of principal component analysis and discriminant analysis in differential sensing routines. Chem. Soc. Rev. 43, 70–84 (2014).
pubmed: 23995750 doi: 10.1039/C3CS60183H
del Villar-Guerra, R., Gray, R. D., Trent, J. O. & Chaires, J. B. A rapid fluorescent indicator displacement assay and principal component/cluster data analysis for determination of ligand–nucleic acid structural selectivity. Nucleic Acids Res. 46, e41 (2018).
pubmed: 29361140 pmcid: 6283418 doi: 10.1093/nar/gky019
Huppert, J. L. Four-stranded nucleic acids: structure, function and targeting of G-quadruplexes. Chem. Soc. Rev. 37, 1375–1384 (2008).
pubmed: 18568163 doi: 10.1039/b702491f
Bochman, M. L., Paeschke, K. & Zakian, V. A. DNA secondary structures: stability and function of G-quadruplex structures. Nat. Rev. Genet. 13, 770–780 (2012).
pubmed: 23032257 pmcid: 3725559 doi: 10.1038/nrg3296
Burge, S. et al. sequence, topology and structure. Nucleic Acids Res. 34, 5402–5415 (2006).
pubmed: 17012276 pmcid: 1636468 doi: 10.1093/nar/gkl655
Dolinnaya, N. G., Ogloblina, A. M. & Yakubovskaya, M. G. Structure, properties, and biological relevance of the DNA and RNA G-quadruplexes: Overview 50 years after their discovery. Biochemistry 81, 1602–1649 (2016).
pubmed: 28260487
Kwok, C. K. & Merrick, C. J. G-quadruplexes: prediction, characterization, and biological application. Trends Biotechnol. 35, 997–1013 (2017).
pubmed: 28755976 doi: 10.1016/j.tibtech.2017.06.012
Puig Lombardi, E. & Londoño-Vallejo, A. A guide to computational methods for G-quadruplex prediction. Nucleic Acids Res. 48, 1–15 (2020).
pubmed: 31754698 doi: 10.1093/nar/gkz1097
Zuffo, M. et al. More is not always better: finding the right trade-off between affinity and selectivity of a G-quadruplex ligand. Nucleic Acids Res. 46, e115 (2018).
pubmed: 29986058 pmcid: 6212845 doi: 10.1093/nar/gky607
Felsenstein, K. M. et al. Small molecule microarrays enable the identification of a selective, quadruplex-binding inhibitor of MYC expression. ACS Chem. Biol. 11, 139–148 (2016).
pubmed: 26462961 doi: 10.1021/acschembio.5b00577
Pinalli, R., Pedrini, A. & Dalcanale, E. Biochemical sensing with macrocyclic receptors. Chem. Soc. Rev. 47, 7006–7026 (2018).
pubmed: 30175351 doi: 10.1039/C8CS00271A
Dsouza, R. N., Hennig, A. & Nau, W. M. Supramolecular tandem enzyme assays. Chem. Eur. J. 18, 3444–3459 (2012).
pubmed: 22367854 doi: 10.1002/chem.201103364
Hennig, A., Bakirci, H. & Nau, W. M. Label-free continuous enzyme assays with macrocycle-fluorescent dye complexes. Nat. Methods 4, 629–632 (2007).
pubmed: 17603491 doi: 10.1038/nmeth1064
Peacor, B. C., Ramsay, C. M. & Waters, M. L. Fluorogenic sensor platform for the histone code using receptors from dynamic combinatorial libraries. Chem. Sci. 8, 1422–1428 (2017).
pubmed: 28451282 doi: 10.1039/C6SC03003C
Minaker, S. A., Daze, K. D., Ma, M. C. F. & Hof, F. Antibody-free reading of the histone code using a simple chemical sensor array. J. Am. Chem. Soc. 134, 11674–11680 (2012).
pubmed: 22703116 doi: 10.1021/ja303465x
Florea, M. & Nau, W. M. Implementation of anion-receptor macrocycles in supramolecular tandem assays for enzymes involving nucleotides as substrates, products, and cofactors. Org. Biomol. Chem. 8, 1033–1039 (2010).
pubmed: 20165793 doi: 10.1039/b925192h
Liu, Y. et al. Selective heavy element sensing with a simple host–guest fluorescent array. Anal. Chem. 89, 11113–11121 (2017).
pubmed: 28946741 doi: 10.1021/acs.analchem.7b03377
Gill, A. D. et al. Sensing of citrulline modifications in histone peptides by deep cavitand hosts. Chem. Commun. 55, 13259–13262 (2019).
doi: 10.1039/C9CC07002H
Murat, P., Singh, Y. & Defrancq, E. Methods for investigating G-quadruplex DNA/ligand interactions. Chem. Soc. Rev. 40, 5293–5307 (2011).
pubmed: 21720638 doi: 10.1039/c1cs15117g
Biros, S. M., Ullrich, E. C., Hof, F., Trembleau, L. & Rebek, J. Kinetically stable complexes in water: the role of hydration and hydrophobicity. J. Am. Chem. Soc. 126, 2870–2876 (2004).
pubmed: 14995204 doi: 10.1021/ja038823m
Liu, Y. et al. Site-selective sensing of histone methylation enzyme activity via an arrayed supramolecular tandem assay. J. Am. Chem. Soc. 139, 10964–10967 (2017).
pubmed: 28777546 pmcid: 5615822 doi: 10.1021/jacs.7b05002
Liu, Y. et al. Selective sensing of phosphorylated peptides and monitoring kinase and phosphatase activity with a supramolecular tandem assay. J. Am. Chem. Soc. 140, 13869–13877 (2018).
pubmed: 30269482 doi: 10.1021/jacs.8b08693
Mosca, S., Yu, Y. & Rebek, J. Preparative scale and convenient synthesis of a water-soluble, deep cavitand. Nat. Protoc. 11, 1371–1387 (2016).
pubmed: 27388554 doi: 10.1038/nprot.2016.078
Pinalli, R. et al. The origin of selectivity in the complexation of N-methyl amino acids by tetraphosphonate cavitands. J. Am. Chem. Soc. 138, 8569–8580 (2016).
pubmed: 27310660 doi: 10.1021/jacs.6b04372
Menozzi, D. et al. Thermodynamics of host–guest interactions between methylpyridinium salts and phosphonate cavitands. Supramol. Chem. 22, 768–775 (2010).
doi: 10.1080/10610278.2010.506547
Yang, Q. et al. Verification of specific G-quadruplex structure by using a novel cyanine dye supramolecular assembly: II. The binding characterization with specific intramolecular G-quadruplex and the recognizing mechanism. Nucleic Acids Res. 38, 1022–1033 (2010).
pubmed: 19933263 doi: 10.1093/nar/gkp1045
Früh, A. E., Artoni, F., Brighenti, R. & Dalcanale, E. Strain field self-diagnostic Poly(dimethylsiloxane) elastomers. Chem. Mater. 29, 7450–7467 (2017).
doi: 10.1021/acs.chemmater.7b02438
Thordarson, P. Determining association constants from titration experiments in supramolecular chemistry. Chem. Soc. Rev. 40, 1305–1323 (2011).
pubmed: 21125111 doi: 10.1039/C0CS00062K
Sengar, A., Heddi, B. & Phan, A. T. Formation of G-quadruplexes in poly-G sequences: structure of a propeller-type parallel-stranded G-quadruplex formed by a G15 stretch. Biochemistry 53, 7718–7723 (2014).
pubmed: 25375976 doi: 10.1021/bi500990v
Ambrus, A. et al. Human telomeric sequence forms a hybrid-type intramolecular G-quadruplex structure with mixed parallel/antiparallel strands in potassium solution. Nucleic Acids Res. 34, 2723–2735 (2006).
pubmed: 16714449 pmcid: 1464114 doi: 10.1093/nar/gkl348

Auteurs

Junyi Chen (J)

Environmental Toxicology Graduate Program, University of California, Riverside, CA, USA.

Briana L Hickey (BL)

Department of Chemistry, University of California, Riverside, CA, USA.

Linlin Wang (L)

Department of Chemistry, University of California, Riverside, CA, USA.

Jiwon Lee (J)

Department of Chemistry, University of California, Riverside, CA, USA.

Adam D Gill (AD)

Department of Biochemistry and Molecular Biology, University of California, Riverside, CA, USA.

Alessia Favero (A)

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
INSTM, UdR, Parma, Italy.

Roberta Pinalli (R)

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
INSTM, UdR, Parma, Italy.

Enrico Dalcanale (E)

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
INSTM, UdR, Parma, Italy.

Richard J Hooley (RJ)

Department of Chemistry, University of California, Riverside, CA, USA. richard.hooley@ucr.edu.
Department of Biochemistry and Molecular Biology, University of California, Riverside, CA, USA. richard.hooley@ucr.edu.

Wenwan Zhong (W)

Environmental Toxicology Graduate Program, University of California, Riverside, CA, USA. wenwan.zhong@ucr.edu.
Department of Chemistry, University of California, Riverside, CA, USA. wenwan.zhong@ucr.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH