Synthesis 2023; 55(20): 3251-3262
DOI: 10.1055/a-2111-2333
feature

New Thiazole Orange Derivatives for Improved Fluorescence Signaling of DNA FIT Probes

Amal Homer
,
Oliver Seitz
We acknowledge support from the Deutsche Forschungsgemeinschaft (DFG), grant Se819/21-1.


Abstract

Forced intercalation probes (FIT probes) are nucleic acid probes in which an intercalator dye of the thiazole orange (TO) family serves as a surrogate nucleobase. Hybridization of FIT probes is accompanied by enhancements of fluorescence. Looking for ways to increase turn-on and brightness of fluorescence, we herein report the synthesis of new fluorogenic base surrogates. In total, nine different TO derivatives were introduced into FIT probes. Fluorescence measurements in six different sequences revealed that substitution at both the quinoline and the benzothiazole part affects fluorescence turn-on upon hybridization and brightness of probe–target duplexes. A TO derivative containing a tricyclic benzothiazole provided FIT probes signaling hybridization by up to 18.6-fold enhancement of fluorescence. Improved fluorescence quantum yields (Φds up to 0.53) and high extinction coefficients (ε518 up to 91000 M–1·cm–1) make this dye an interesting, and in some sequences superior, alternative to the canonical thiazole orange used previously in FIT probes.

Supporting Information



Publication History

Received: 28 April 2023

Accepted after revision: 15 June 2023

Accepted Manuscript online:
15 June 2023

Article published online:
19 July 2023

© 2023. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

    • 1a Buxbaum AR, Haimovich G, Singer RH. Nat. Rev. Mol. Cell Biol. 2015; 16: 95
    • 1b Faltin B, Zengerle R, von Stetten F. Clin. Chem. 2013; 59: 1567
    • 1c Tomoike F, Abe H. Adv. Drug Delivery Rev. 2019; 147: 44
    • 2a Cardullo RA, Agrawal S, Flores C, Zamecnik PC, Wolf DE. Proc. Natl. Acad. Sci. U. S. A. 1988; 85: 8790
    • 2b Martí AA, Jockusch S, Stevens N, Ju J, Turro NJ. Acc. Chem. Res. 2007; 40: 402
    • 2c Kolpashchikov DM. Chem. Rev. 2010; 110: 4709
  • 3 Holland PM, Abramson RD, Watson R, Gelfand DH. Proc. Natl. Acad. Sci. U. S. A. 1991; 88: 7276
    • 4a Tyagi S, Kramer FR. Nat. Biotechnol. 1996; 14: 303
    • 4b Bonnet G, Tyagi S, Libchaber A, Kramer FR. Proc. Natl. Acad. Sci. U. S. A. 1999; 96: 6171
  • 5 Yang CJ, Lin H, Tan W. J. Am. Chem. Soc. 2005; 127: 12772
  • 6 Tyagi S, Marras SA, Kramer FR. Nat. Biotechnol. 2000; 18: 1191
  • 7 Jayagopal A, Halfpenny KC, Perez JW, Wright DW. J. Am. Chem. Soc. 2010; 132: 9789
  • 8 Haner R, Biner SM, Langenegger SM, Meng T, Malinovskii VL. Angew. Chem. Int. Ed. 2010; 49: 1227
  • 9 Grossmann TN, Röglin L, Seitz O. Angew. Chem. Int. Ed. 2007; 46: 5223
  • 10 Holzhauser C, Wagenknecht H.-A. ChemBioChem 2012; 13: 1136
  • 11 Lin YW, Ho HT, Huang CC, Chang HT. Nucleic Acids Res. 2008; 36: e123
  • 12 Wang L, Yang CJ, Medley CD, Benner SA, Tan W. J. Am. Chem. Soc. 2005; 127: 15664
  • 13 Roth M, Seitz O. Chem. Eur. J. 2021; 27: 14189
  • 14 Hövelmann F, Seitz O. Acc. Chem. Res. 2016; 49: 714
  • 15 Ishiguro T, Saitoh J, Yawata H, Otsuka M, Inoue T, Sugiura Y. Nucleic Acids Res. 1996; 24: 4992
    • 17a Seitz O, Bergmann F, Heindl D. Angew. Chem. Int. Ed. 1999; 38: 2203
    • 17b Köhler O, Seitz O. Chem. Commun. 2003; 2938
  • 18 Köhler O, Jarikote DV, Seitz O. ChemBioChem 2005; 6: 69
  • 19 Bethge L, Singh I, Seitz O. Org. Biomol. Chem. 2010; 8: 2439
  • 20 Hövelmann F, Bethge L, Seitz O. ChemBioChem 2012; 13: 2072
  • 21 Karunakaran V, Pérez Lustres JL, Zhao L, Ernsting NP, Seitz O. J. Am. Chem. Soc. 2006; 128: 2954
  • 22 Jarikote DV, Krebs N, Tannert S, Röder B, Seitz O. Chem. Eur. J. 2007; 13: 300
  • 23 Socher E, Jarikote DV, Knoll A, Röglin L, Burmeister J, Seitz O. Anal. Biochem. 2008; 375: 318
  • 24 Knoll A, Kankowski S, Schöllkopf S, Meier JC, Seitz O. Chem. Commun. 2019; 55: 14817
  • 25 Hövelmann F, Gaspar I, Loibl S, Ermilov EA, Röder B, Wengel J, Ephrussi A, Seitz O. Angew. Chem. Int. Ed. 2014; 53: 11370
  • 26 Hövelmann F, Gaspar I, Chamiolo J, Kasper M, Steffen J, Ephrussi A, Seitz O. Chem. Sci. 2016; 7: 128
    • 27a Gaspar I, Hövelmann F, Chamiolo J, Ephrussi A, Seitz O. ACS Chem. Biol. 2018; 13: 742
    • 27b Chamiolo J, Fang G.-M, Hövelmann F, Friedrich D, Knoll A, Loewer A, Seitz O. ChemBioChem 2019; 20: 595
    • 27c Torres AG, Fabani MM, Vigorito E, Williams D, Al-Obaidi N, Wojciechowski F, Hudson RH, Seitz O, Gait MJ. Nucleic Acids Res. 2012; 40: 2152
    • 27d Kam Y, Rubinstein A, Nissan A, Halle D, Yavin E. Mol. Pharmaceutics 2012; 9: 685
    • 27e Kolevzon N, Hashoul D, Naik S, Rubinstein A, Yavin E. Chem. Commun. 2016; 52: 2405
    • 27f Sonar MV, Wampole ME, Jin Y.-Y, Chen C.-P, Thakur ML, Wickstrom E. Bioconjugate Chem. 2014; 25: 1697
  • 28 Fang G.-M, Chamiolo J, Kankowski S, Hövelmann F, Friedrich D, Löwer A, Meier JC, Seitz O. Chem. Sci. 2018; 9: 4794
  • 29 Sato T, Sato Y, Nishizawa S. J. Am. Chem. Soc. 2016; 138: 9397
    • 30a Ebrahimi SB, Samanta D, Cheng HF, Nathan LI, Mirkin CA. J. Am. Chem. Soc. 2019; 141: 13744
    • 30b Ebrahimi SB, Samanta D, Partridge BE, Kusmierz CD, Cheng HF, Grigorescu AA, Chávez JL, Mirau PA, Mirkin CA. Angew. Chem. Int. Ed. 2021; 60: 15260
  • 31 Socher E, Knoll A, Seitz O. Org. Biomol. Chem. 2012; 10: 7363
  • 32 Bethge L, Jarikote DV, Seitz O. Bioorg. Med. Chem. 2008; 16: 114
  • 33 Uno K, Sasaki T, Sugimoto N, Ito H, Nishihara T, Hagihara S, Higashiyama T, Sasaki N, Sato Y, Itami K. Chem. Asian J. 2017; 12: 233
  • 34 Zhou CY, Alexander SC, Devaraj NK. Chem. Sci. 2017; 8: 7169
  • 35 McDougall M, Dwight SJ. US9206474B2, 2015
  • 36 Saarnio VK, Alaranta JM, Lahtinen TM. J. Mater. Chem. B 2021; 9: 3484
  • 37 Long W, Lu Y.-J, Zhang K, Huang X.-H, Hou J.-Q, Cai S.-Y, Li Y, Du X, Luyt LG, Wong W.-L, Chow C.-F. Dyes Pigm. 2018; 159: 449
  • 38 Seitz O, Ficht S, Röglin L, Ziehe M, Breyer D. Synlett 2004; 2525
  • 39 Owczarzy R, Tataurov AV, Wu Y, Manthey JA, McQuisten KA, Almabrazi HG, Pedersen KF, Lin Y, Garretson J, McEntaggart NO, Sailor CA, Dawson RB, Peek AS. Nucleic Acids Res. 2008; 36: W163
  • 40 Cavazos-Elizondo D, Aguirre-Soto A. Analysis Sensing 2022; 2: e202200004