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-Calvo1,3(), Sandra A. Bright1,2, Emma B. Veale1, Adam F. Henwood1, D. Clive Williams2, Thorfinnur Gunnlaugsson1()
1. School of Chemistry and Trinity Biomedical Sciences Institute (TBSI), Trinity College Dublin, The University of Dublin, Dublin 2, Ireland 2. School of Biochemistry and Immunology and Trinity Biomedical Sciences Institute (TBSI), Trinity College Dublin, The University of Dublin, Dublin 2, Ireland 3. Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS) and Departamento de Química Orgánica Universidade de Santiago de Compostela, Rúa Jenaro de la Fuente s/n, 15782, Santiago de Compostela, Spain
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.
Corresponding Author(s):
Miguel Martínez-Calvo,Thorfinnur Gunnlaugsson
引用本文:
. [J]. Frontiers of Chemical Science and Engineering, 2020, 14(1): 61-75.
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. Front. Chem. Sci. Eng., 2020, 14(1): 61-75.
D Wu, A C Sedgwick, T Gunnlaugsson, E U Akkaya, J Yoon, T D James. Fluorescent chemosensors: The past, present and future. Chemical Society Reviews, 2017, 46(23): 7105–7123
2
C J Chang, T Gunnlaugsson, T D James. Sensor targets. Chemical Society Reviews, 2015, 44(13): 4176–4178 https://doi.org/10.1039/C5CS90058A
3
J R Casey, S Grinstein, J Orlowski. Sensors and regulators of intracellular pH. Nature Reviews. Molecular Cell Biology, 2010, 11(1): 50–61 https://doi.org/10.1038/nrm2820
4
H A Clark, M Hoyer, M A Philbert, R Kopelman. 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 https://doi.org/10.1021/ac990629o
5
E B Veale, T Gunnlaugsson. Fluorescent sensors for ions based on organic structures. Annual Reports Section “B” (Organic Chemistry), 2010, 106: 376–406
B Daly, J Ling, A P de Silva. Current developments in fluorescent PET (photoinduced electron transfer) sensors and switches. Chemical Society Reviews, 2015, 44(13): 4203–4211 https://doi.org/10.1039/C4CS00334A
8
R M Duke, E B Veale, F M Pfeffer, P E Kruger, T Gunnlaugsson. 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 https://doi.org/10.1039/b910560n
9
S Banerjee, E B Veale, C M Phelan, S A Murphy, G M Tocci, L J Gillespie, D O Frimannsson, J M Kelly, T Gunnlaugsson. 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 https://doi.org/10.1039/c2cs35467e
10
S Shanmugaraju, B la Cour Poulsen, T Arisa, D Umadevi, H L Dalton, C S Hawes, A J Savyasachi, G W Watson, D C Williams, T Gunnlaugsson. 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 https://doi.org/10.1039/C8CC01584H
11
S Shanmugaraju, C S Hawes, A J Savyasachi, S Blasco, J A Kitchen, T Gunnlaugsson. 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 https://doi.org/10.1039/C7CC07333J
12
S Shanmugaraju, D McAdams, F Pancotti, C S Hawes, E B Veale, J A Kitchen, T Gunnlaugsson. 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 https://doi.org/10.1039/C7OB01835E
13
S Shanmugaraju, C Dabadie, K Byrne, A J Savyasachi, D Umadevi, W Schmitt, J A Kitchen, T Gunnlaugsson. 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 https://doi.org/10.1039/C6SC04367D
14
Y Tian, F Su, W Weber, V Nandakumar, B R Shumway, Y Jin, X Zhou, M R Holl, R H Johnson, D R Meldrum. A series of naphthalimide derivatives as intra and extracellular pH sensors. Biomaterials, 2010, 31(29): 7411–7422 https://doi.org/10.1016/j.biomaterials.2010.06.023
15
X Ao, S A Bright, N C Taylor, R B P Elmes. 2-Nitroimidazole based fluorescent probes for nitroreductase; monitoring reductive stress in cellulo. Organic & Biomolecular Chemistry, 2017, 15(29): 6104–6108 https://doi.org/10.1039/C7OB01406F
16
T Jia, C Fu, C Huang, H Yang, N Jia. Highly sensitive naphthalimide-based fluorescence polarization probe for detecting cancer cells. ACS Applied Materials & Interfaces, 2015, 7(18): 10013–10021 https://doi.org/10.1021/acsami.5b02429
17
M H Lee, J H Han, P S Kwon, S Bhuniya, J Y Kim, J L Sessler, C Kang, J S Kim. 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 https://doi.org/10.1021/ja210065g
18
L Dong, Y Zang, D Zhou, X P He, G R Chen, T D James, J Li. Glycosylation enhances the aqueous sensitivity and lowers the cytotoxicity of a naphthalimide zinc ion fluorescence probe. Chemical Communications, 2015, 51(59): 11852–11855 https://doi.org/10.1039/C5CC04357C
19
X Li, Y Lin, Q Wang, Y Yuan, H Zhang, X Qian. 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 https://doi.org/10.1016/j.ejmech.2011.01.050
20
L Zhang, K Lei, J Zhang, W Song, Y Zheng, S Tan, Y Gao, Y Xu, J Liu, X Qian. One small molecule as a theranostic agent: Naphthalimide dye for subcellular fluorescence localization and photodynamic therapy in vivo. MedChemComm, 2016, 7(6): 1171–1175 https://doi.org/10.1039/C6MD00104A
21
S Banerjee, J A Kitchen, T Gunnlaugsson, J M Kelly. 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 https://doi.org/10.1039/c3ob40370j
22
S Banerjee, J A Kitchen, T Gunnlaugsson, J M Kelly. 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 https://doi.org/10.1039/c2ob06898b
23
M Li, Z Guo, W Zhu, F Marken, T D James. A redox-activated fluorescence switch based on a ferrocene–fluorophore–boronic ester conjugate. Chemical Communications, 2015, 51(7): 1293–1296 https://doi.org/10.1039/C4CC07891H
24
M Li, H Ge, V Mirabello, R L Arrowsmith, G Kociok-Kohn, S W Botchway, W Zhu, S I Pascu, T D James. Lysosomal tracking with a cationic naphthalimide using multiphoton fluorescence lifetime imaging microscopy. Chemical Communications, 2017, 53(81): 11161–11164 https://doi.org/10.1039/C7CC05166B
25
M Li, H Ge, R L Arrowsmith, V Mirabello, S W Botchway, W Zhu, S I Pascu, T D James. Ditopic boronic acid and imine-based naphthalimide fluorescence sensor for copper(II). Chemical Communications, 2014, 50(80): 11806–11809 https://doi.org/10.1039/C4CC03453H
26
K N Hearn, T D Nalder, R P Cox, H D Maynard, T D M Bell, F M Pfeffer, T D Ashton. Modular synthesis of 4-aminocarbonyl substituted 1,8-naphthalimides and application in single molecule fluorescence detection. Chemical Communications, 2017, 53(91): 12298–12301 https://doi.org/10.1039/C7CC07922B
27
C L Fleming, A Natoli, J Schreuders, M Devlin, P Yoganantharajah, Y Gibert, K G Leslie, E J New, T D Ashton, F M Pfeffer. Highly fluorescent and HDAC6 selective scriptaid analogues. European Journal of Medicinal Chemistry, 2019, 162: 321–333 https://doi.org/10.1016/j.ejmech.2018.11.020
28
J C Spiteri, A D Johnson, S A Denisov, G Jonusauskas, N D McClenaghan, D C Magri. A fluorescent AND logic gate based on a ferrocene-naphthalimide-piperazine format responsive to acidity and oxidizability. Dyes and Pigments, 2018, 157: 278–283 https://doi.org/10.1016/j.dyepig.2018.04.060
29
J C Spiteri, S A Denisov, G Jonusauskas, S Klejna, K Szacilowski, N D McClenaghan, D C Magri. 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 https://doi.org/10.1039/C8OB00485D
30
A D Johnson, K A Paterson, J C Spiteri, S A Denisov, G Jonusauskas, A Tron, D C Magri. 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 https://doi.org/10.1039/C6NJ02023B
31
S Banerjee, J A Kitchen, S A Bright, J E O’Brien, D C Williams, J M Kelly, T Gunnlaugsson. 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 https://doi.org/10.1039/c3cc44962a
32
E Calatrava-Pérez, S A Bright, S Achermann, C Moylan, M O Senge, E B Veale, D C Williams, T Gunnlaugsson, E M Scanlan. Glycosidase activated release of fluorescent 1,8-naphthalimide probes for tumor cell imaging from glycosylated ‘Pro-probes’. Chemical Communications, 2016, 52(89): 13086–13089 https://doi.org/10.1039/C6CC06451E
33
R B P Elmes, M Erby, S A Bright, D C Williams, T Gunnlaugsson. 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 https://doi.org/10.1039/c2cc17274g
34
S Zheng, P L M Lynch, T E Rice, T S Moody, H Q N Gunaratne, A P de Silva. Structural effects on the pH-dependent fluorescence of naphthalenic derivatives and consequences for sensing/switching. Photochemical & Photobiological Sciences, 2012, 11(11): 1675–1681 https://doi.org/10.1039/c2pp25069a
35
B Daly, J Ling, A P de Silva. Current developments in fluorescent PET (photoinduced electron transfer) sensors and switches. Chemical Society Reviews, 2015, 44(13): 4203–4211 https://doi.org/10.1039/C4CS00334A
36
E Calatrava-Pérez, J M Delente, S Shanmugaraju, C S Hawes, C D Williams, T Gunnlaugsson, E M Scanlan. Glycosylated naphthalimides and naphthalimide Tröger’s bases as fluorescent aggregation probes for Con A. Organic & Biomolecular Chemistry, 2019, 7(8): 2116–2125 https://doi.org/10.1039/C8OB02980F
37
R M Duke, T Gunnlaugsson. 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 https://doi.org/10.1016/j.tetlet.2011.01.099
38
T Gunnlaugsson, C P McCoy, R J Morrow, C Phelan, F Stomeo. 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
A P de Silva, H Q N Gunaratne, J L Habib-Jiwan, C P McCoy, T E Rice, J P Soumillion. 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 https://doi.org/10.1002/anie.199517281
40
E B Veale, T Gunnlaugsson. 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 https://doi.org/10.1021/jo8012594
41
T E Rice, A P de Silva. 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
D C Magri, A P de Silva. 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 https://doi.org/10.1039/b9nj00564a
43
E B Veale, J A Kitchen, T Gunnlaugsson. 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 https://doi.org/10.1080/10610278.2012.752088
44
J Qian, Y Xu, X Qian, J Wang, S Zhang. 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 https://doi.org/10.1016/j.jphotochem.2008.09.002
45
L Zhou, Z Jin, X Fan, Y Yao, C Zhaoyang, W Zhang, J Qian. Synthesis of 1,8-naphthalimide-based fluorescent nano-probes and their application in pH detection. Chinese Chemical Letters, 2018, 29(10): 1500–1502 https://doi.org/10.1016/j.cclet.2018.07.018
46
A P de Silva, H Q N Gunaratne, T Gunnlaugsson, P L M Lynch. Molecular photoionic switches with an internal reference channel for fluorescent pH sensing applications. New Journal of Chemistry, 1996, 20(7-8): 871
47
Y Q Gao, R A Marcus. Theoretical investigation of the directional electron transfer in 4-aminonaphthalimide compounds. Journal of Physical Chemistry A, 2002, 106(10): 1956–1960 https://doi.org/10.1021/jp011980s
48
E B Veale, T Gunnlaugsson. 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 https://doi.org/10.1021/jo1005697
49
G J Ryan, F E Poynton, R B P Elmes, M Erby, D C Williams, S J Quinn, T Gunnlaugsson. 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 https://doi.org/10.1039/C5DT00360A