4-Amino-1,8-naphthalimide based fluorescent photoinduced electron transfer (PET) pH sensors as liposomal cellular imaging agents: The effect of substituent patterns on PET directional quenching
Miguel Martínez-Calvo, Sandra A. Bright, Emma B. Veale, Adam F. Henwood, D. Clive Williams, Thorfinnur Gunnlaugsson
4-Amino-1,8-naphthalimide based fluorescent photoinduced electron transfer (PET) pH sensors as liposomal cellular imaging agents: The effect of substituent patterns on PET directional quenching
Four new fluorescent sensors (1-4) based on the 4-amino-1,8-naphthalimide fluorophores (Naps) have been synthesized based on the classical fluorophore-spacer-receptor model. These four compounds all gave rise to emission bands centred at ca. 535 nm, which were found to be highly pH dependent, the emission being ‘switched on’ in acidic media, while being quenched due to PET from the amino moieties to the excited state of the Nap at more alkaline pH. The luminescent pH dependence for these probes was found to be highly dependent on the substitution on the imide site, as well as the polyamine chain attached to the position 4-amino moiety. In the case of sensor 2 the presence of the 4-amino-aniline dominated the pH dependent quenching. Nevertheless, at higher pH, PET quenching was also found to occur from the polyamine site. Hence, 2 is better described as a receptor1-spacer1-fluorophore-spacer2-receptor2 system, where the dominant PET process is due to (normally less favourable) ‘directional’ PET quenching from the 4-amino-aniline unit to the Nap site. Similar trends and pH fluorescence dependences were also seen for 3 and 4. These compounds were also tested for their imaging potential and toxicity against HeLa cells (using DRAQ5 as nuclear stain which does now show pH dependent changes in acidic and neutral pH) and the results demonstrated that these compounds have reduced cellular viability at moderately high concentrations (with IC50 values between ca. 8–30 µmol∙L−1), but were found to be suitable for intracellular pH determination at 1 µmol∙L−1concentrations, where no real toxicity was observed. This allowed us to employ these as lysosomal probes at sub-toxic concentrations, where the Nap based emission was found to be pH depended, mirroring that seen in aqueous solution for 1-4, with the main fluorescence changes occurring within acidic to neutral pH.
sensors / pH / photoinduced electron transfer / cellular imaging / confocal microscopy
[1] |
Wu D, Sedgwick A C, Gunnlaugsson T, Akkaya E U, Yoon J, James T D. Fluorescent chemosensors: The past, present and future. Chemical Society Reviews, 2017, 46(23): 7105–7123
|
[2] |
Chang C J, Gunnlaugsson T, James T D. Sensor targets. Chemical Society Reviews, 2015, 44(13): 4176–4178
CrossRef
Google scholar
|
[3] |
Casey J R, Grinstein S, Orlowski J. Sensors and regulators of intracellular pH. Nature Reviews. Molecular Cell Biology, 2010, 11(1): 50–61
CrossRef
Google scholar
|
[4] |
Clark H A, Hoyer M, Philbert M A, Kopelman R. Optical nanosensors for chemical analysis inside single living cells. 1. Sensors for pH and calcium and the intracellular application of PEBBLE sensors I. Analytical Chemistry, 1999, 71(21): 4831–4836
CrossRef
Google scholar
|
[5] |
Veale E B, Gunnlaugsson T. Fluorescent sensors for ions based on organic structures. Annual Reports Section “B” (Organic Chemistry), 2010, 106: 376–406
|
[6] |
Han J, Burgess K. Indicators for intracellular pH. Chemical Reviews, 2010, 110(5): 2709–2728
CrossRef
Google scholar
|
[7] |
Daly B, Ling J, de Silva A P. Current developments in fluorescent PET (photoinduced electron transfer) sensors and switches. Chemical Society Reviews, 2015, 44(13): 4203–4211
CrossRef
Google scholar
|
[8] |
Duke R M, Veale E B, Pfeffer F M, Kruger P E, Gunnlaugsson T. Colorimetric and fluorescent anion sensors: An overview of recent developments in the use of 1,8-naphthalimide-based chemosensors. Chemical Society Reviews, 2010, 39(10): 3936–3953
CrossRef
Google scholar
|
[9] |
Banerjee S, Veale E B, Phelan C M, Murphy S A, Tocci G M, Gillespie L J, Frimannsson D O, Kelly J M, Gunnlaugsson T. Recent advances in the development of 1,8-naphthalimide based DNA targeting binders, anticancer and fluorescent cellular imaging agents. Chemical Society Reviews, 2013, 42(4): 1601–1618
CrossRef
Google scholar
|
[10] |
Shanmugaraju S, la Cour Poulsen B, Arisa T, Umadevi D, Dalton H L, Hawes C S, Savyasachi A J, Watson G W, Williams D C, Gunnlaugsson T. Synthesis, structural characterisation and antiproliferative activity of a new fluorescent 4-amino-1,8-naphthalimide Tröger’s base-Ru(II)-curcumin organometallic conjugate. Chemical Communications, 2018, 54(33): 4120–4123
CrossRef
Google scholar
|
[11] |
Shanmugaraju S, Hawes C S, Savyasachi A J, Blasco S, Kitchen J A, Gunnlaugsson T. Supramolecular coordination polymers using a close to ‘V-shaped’ fluorescent 4-amino-1,8-naphthalimide Tröger’s base scaffold. Chemical Communications, 2017, 53(93): 12512–12515
CrossRef
Google scholar
|
[12] |
Shanmugaraju S, McAdams D, Pancotti F, Hawes C S, Veale E B, Kitchen J A, Gunnlaugsson T. One-pot facile synthesis of 4-amino-1,8-naphthalimide derived Tröger’s bases via a nucleophilic displacement approach. Organic & Biomolecular Chemistry, 2017, 15(35): 7321–7329
CrossRef
Google scholar
|
[13] |
Shanmugaraju S, Dabadie C, Byrne K, Savyasachi A J, Umadevi D, Schmitt W, Kitchen J A, Gunnlaugsson T. A supramolecular Tröger’s base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water. Chemical Science (Cambridge), 2017, 8(2): 1535–1546
CrossRef
Google scholar
|
[14] |
Tian Y, Su F, Weber W, Nandakumar V, Shumway B R, Jin Y, Zhou X, Holl M R, Johnson R H, Meldrum D R. A series of naphthalimide derivatives as intra and extracellular pH sensors. Biomaterials, 2010, 31(29): 7411–7422
CrossRef
Google scholar
|
[15] |
Ao X, Bright S A, Taylor N C, Elmes R B P. 2-Nitroimidazole based fluorescent probes for nitroreductase; monitoring reductive stress in cellulo. Organic & Biomolecular Chemistry, 2017, 15(29): 6104–6108
CrossRef
Google scholar
|
[16] |
Jia T, Fu C, Huang C, Yang H, Jia N. Highly sensitive naphthalimide-based fluorescence polarization probe for detecting cancer cells. ACS Applied Materials & Interfaces, 2015, 7(18): 10013–10021
CrossRef
Google scholar
|
[17] |
Lee M H, Han J H, Kwon P S, Bhuniya S, Kim J Y, Sessler J L, Kang C, Kim J S. Hepatocyte-targeting single galactose-appended naphthalimide: A tool for intracellular thiol imaging in vivo. Journal of the American Chemical Society, 2012, 134(2): 1316–1322
CrossRef
Google scholar
|
[18] |
Dong L, Zang Y, Zhou D, He X P, Chen G R, James T D, Li J. Glycosylation enhances the aqueous sensitivity and lowers the cytotoxicity of a naphthalimide zinc ion fluorescence probe. Chemical Communications, 2015, 51(59): 11852–11855
CrossRef
Google scholar
|
[19] |
Li X, Lin Y, Wang Q, Yuan Y, Zhang H, Qian X. The novel anti-tumor agents of 4-triazol-1,8-naphthalimides: Synthesis, cytotoxicity, DNA intercalation and photocleavage. European Journal of Medicinal Chemistry, 2011, 46(4): 1274–1279
CrossRef
Google scholar
|
[20] |
Zhang L, Lei K, Zhang J, Song W, Zheng Y, Tan S, Gao Y, Xu Y, Liu J, Qian X. One small molecule as a theranostic agent: Naphthalimide dye for subcellular fluorescence localization and photodynamic therapy in vivo. MedChemComm, 2016, 7(6): 1171–1175
CrossRef
Google scholar
|
[21] |
Banerjee S, Kitchen J A, Gunnlaugsson T, Kelly J M. The effect of the 4-amino functionality on the photophysical and DNA binding properties of alkyl-pyridinium derived 1,8-naphthalimides. Organic & Biomolecular Chemistry, 2013, 11(34): 5642–5655
CrossRef
Google scholar
|
[22] |
Banerjee S, Kitchen J A, Gunnlaugsson T, Kelly J M. Synthesis and photophysical evaluation of a pyridinium 4-amino-1,8-naphthalimide derivative that upon intercalation displays preference for AT- rich double-stranded DNA. Organic & Biomolecular Chemistry, 2012, 10(15): 3033–3043
CrossRef
Google scholar
|
[23] |
Li M, Guo Z, Zhu W, Marken F, James T D. A redox-activated fluorescence switch based on a ferrocene–fluorophore–boronic ester conjugate. Chemical Communications, 2015, 51(7): 1293–1296
CrossRef
Google scholar
|
[24] |
Li M, Ge H, Mirabello V, Arrowsmith R L, Kociok-Kohn G, Botchway S W, Zhu W, Pascu S I, James T D. Lysosomal tracking with a cationic naphthalimide using multiphoton fluorescence lifetime imaging microscopy. Chemical Communications, 2017, 53(81): 11161–11164
CrossRef
Google scholar
|
[25] |
Li M, Ge H, Arrowsmith R L, Mirabello V, Botchway S W, Zhu W, Pascu S I, James T D. Ditopic boronic acid and imine-based naphthalimide fluorescence sensor for copper(II). Chemical Communications, 2014, 50(80): 11806–11809
CrossRef
Google scholar
|
[26] |
Hearn K N, Nalder T D, Cox R P, Maynard H D, Bell T D M, Pfeffer F M, Ashton T D. Modular synthesis of 4-aminocarbonyl substituted 1,8-naphthalimides and application in single molecule fluorescence detection. Chemical Communications, 2017, 53(91): 12298–12301
CrossRef
Google scholar
|
[27] |
Fleming C L, Natoli A, Schreuders J, Devlin M, Yoganantharajah P, Gibert Y, Leslie K G, New E J, Ashton T D, Pfeffer F M. Highly fluorescent and HDAC6 selective scriptaid analogues. European Journal of Medicinal Chemistry, 2019, 162: 321–333
CrossRef
Google scholar
|
[28] |
Spiteri J C, Johnson A D, Denisov S A, Jonusauskas G, McClenaghan N D, Magri D C. A fluorescent AND logic gate based on a ferrocene-naphthalimide-piperazine format responsive to acidity and oxidizability. Dyes and Pigments, 2018, 157: 278–283
CrossRef
Google scholar
|
[29] |
Spiteri J C, Denisov S A, Jonusauskas G, Klejna S, Szacilowski K, McClenaghan N D, Magri D C. Molecular engineering of logic gate types by module rearrangement in ‘Pourbaix sensors’: The effect of excited-state electric fields. Organic & Biomolecular Chemistry, 2018, 16(34): 6195–6201
CrossRef
Google scholar
|
[30] |
Johnson A D, Paterson K A, Spiteri J C, Denisov S A, Jonusauskas G, Tron A, Magri D C. Water-soluble naphthalimide-based “Pourbaix sensors”: pH and redox-activated fluorescent AND logic gates based on photoinduced electron transfer. New Journal of Chemistry, 2016, 40(12): 9917–9922
CrossRef
Google scholar
|
[31] |
Banerjee S, Kitchen J A, Bright S A, O’Brien J E, Williams D C, Kelly J M, Gunnlaugsson T. Synthesis, spectroscopic and biological studies of a fluorescent Pt(II) (terpy) based 1,8-naphthalimide conjugate as a DNA targeting agent. Chemical Communications, 2013, 49(76): 8522–8524
CrossRef
Google scholar
|
[32] |
Calatrava-Pérez E, Bright S A, Achermann S, Moylan C, Senge M O, Veale E B, Williams D C, Gunnlaugsson T, Scanlan E M. Glycosidase activated release of fluorescent 1,8-naphthalimide probes for tumor cell imaging from glycosylated ‘Pro-probes’. Chemical Communications, 2016, 52(89): 13086–13089
CrossRef
Google scholar
|
[33] |
Elmes R B P, Erby M, Bright S A, Williams D C, Gunnlaugsson T. Photophysical and biological investigation of novel luminescent Ru(II)-polypyridyl-1,8-naphthalimide Tröger’s bases as cellular imaging agents. Chemical Communications, 2012, 48(20): 2588–2590
CrossRef
Google scholar
|
[34] |
Zheng S, Lynch P L M, Rice T E, Moody T S, Gunaratne H Q N, de Silva A P. Structural effects on the pH-dependent fluorescence of naphthalenic derivatives and consequences for sensing/switching. Photochemical & Photobiological Sciences, 2012, 11(11): 1675–1681
CrossRef
Google scholar
|
[35] |
Daly B, Ling J, de Silva A P. Current developments in fluorescent PET (photoinduced electron transfer) sensors and switches. Chemical Society Reviews, 2015, 44(13): 4203–4211
CrossRef
Google scholar
|
[36] |
Calatrava-Pérez E, Delente J M, Shanmugaraju S, Hawes C S, Williams C D, Gunnlaugsson T, Scanlan E M. Glycosylated naphthalimides and naphthalimide Tröger’s bases as fluorescent aggregation probes for Con A. Organic & Biomolecular Chemistry, 2019, 7(8): 2116–2125
CrossRef
Google scholar
|
[37] |
Duke R M, Gunnlaugsson T. 3-Urea-1,8-naphthalimides are good chemosensors: A highly selective dual colorimetric and fluorescent ICT based anion sensor for fluoride. Tetrahedron Letters, 2011, 52(13): 1503–1505
CrossRef
Google scholar
|
[38] |
Gunnlaugsson T, McCoy C P, Morrow R J, Phelan C, Stomeo F. Towards the development of controllable and reversible ‘on-off’ luminescence switching in soft-matter: Synthesis and spectroscopic investigation of 1,8-naphthalimide-based PET (photoinduced electron transfer) chemosensors for pH in water-permeable hydrogels. ARKIVOC, 2003, 7: 216–228
|
[39] |
de Silva A P, Gunaratne H Q N, Habib-Jiwan J L, McCoy C P, Rice T E, Soumillion J P. New fluorescent model compounds for the study of photoinduced electron transfer: The influence of a molecular electric field in the excited state. Angewandte Chemie International Edition in English, 1995, 34(16): 1728–1731
CrossRef
Google scholar
|
[40] |
Veale E B, Gunnlaugsson T. Bi-directional photoinduced electron transfer (PET) quenching is observed in 4-amino-1,8-naphthalimide based fluorescent anion sensors. Journal of Organic Chemistry, 2008, 73(20): 8073–7076
CrossRef
Google scholar
|
[41] |
Rice T E, de Silva A P. A small supramolecular system which emulates the unidirectional, path-selective photoinduced electron transfer (PET) of the bacterial photosynthetic reaction centre (PRC). Chemical Communications, 1999: 163–164
|
[42] |
Magri D C, de Silva A P. From PASS 1 to YES to AND logic: Building parallel processing into molecular logic gates by sequential addition of receptors. New Journal of Chemistry, 2010, 34(3): 476–481
CrossRef
Google scholar
|
[43] |
Veale E B, Kitchen J A, Gunnlaugsson T. Fluorescent tren-based 4-amino-1,8-naphthalimide sensor for Cu(II) based on the use of the (fluorophore-spacer-receptor) photoinduced electron transfer (PET) principle. Supramolecular Chemistry, 2013, 25(2): 101–108
CrossRef
Google scholar
|
[44] |
Qian J, Xu Y, Qian X, Wang J, Zhang S. Effects of anionic surfactant SDS on the photophysical properties of two fluorescent molecular sensors. Journal of Photochemistry and Photobiology A Chemistry, 2008, 200(2-3): 402–409
CrossRef
Google scholar
|
[45] |
Zhou L, Jin Z, Fan X, Yao Y, Zhaoyang C, Zhang W, Qian J. Synthesis of 1,8-naphthalimide-based fluorescent nano-probes and their application in pH detection. Chinese Chemical Letters, 2018, 29(10): 1500–1502
CrossRef
Google scholar
|
[46] |
de Silva A P, Gunaratne H Q N, Gunnlaugsson T, Lynch P L M. Molecular photoionic switches with an internal reference channel for fluorescent pH sensing applications. New Journal of Chemistry, 1996, 20(7-8): 871
|
[47] |
Gao Y Q, Marcus R A. Theoretical investigation of the directional electron transfer in 4-aminonaphthalimide compounds. Journal of Physical Chemistry A, 2002, 106(10): 1956–1960
CrossRef
Google scholar
|
[48] |
Veale E B, Gunnlaugsson T. Synthesis, photophysical and DNA binding studies of fluorescent Tröger’s base derived 4-amino-1,8-naphthalimide supramolecular clefts. Journal of Organic Chemistry, 2010, 75(16): 5513–5525
CrossRef
Google scholar
|
[49] |
Ryan G J, Poynton F E, Elmes R B P, Erby M, Williams D C, Quinn S J, Gunnlaugsson T. Unexpected DNA binding properties with correlated downstream biological applications in mono vs. bis-1,8-naphthalimide Ru(II)-polypyridyl conjugates. Dalton Transactions (Cambridge, England), 2015, 44(37): 16332–16344
CrossRef
Google scholar
|
/
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