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Multicolored pH-Tunable and Activatable Fluorescence Nanoplatform Responsive to Physiologic pH Stimuli
Open accessAbstract
Tunable, ultra-pH responsive fluorescent nanoparticles with multichromatic emissions are highly valuable in a variety of biological studies, such as endocytic trafficking, endosome/lysosome maturation, and pH regulation in subcellular organelles. Small differences (e.g., <1 pH unit) and yet finely regulated physiological pH inside different endocytic compartments present a huge challenge to the design of such a system. Herein, we report a general strategy to produce pH-tunable, highly activatable multicolored fluorescent nanoparticles using commonly available pH-insensitive dyes with emission wavelengths from green to near IR range. The primary driving force of fluorescence activation between the ON (unimer) and OFF (micelle) states is the pH-induced micellization. Among three possible photochemical mechanisms, homo Förster resonance energy transfer (homoFRET)-enhanced decay was found to be the most facile strategy to render ultra-pH response over the H-dimer and photoinduced electron transfer (PeT) mechanisms. Based on this insight, we selected several fluorophores with small Stoke shifts (<40 nm) and established a panel of multicolored nanoparticles with wide emission range (500-820 nm) and different pH transitions. Each nanoparticle maintained the sharp pH response (ON/OFF < 0.25 pH unit) with corresponding pH transition point at pH 5.2, 6.4, 6.9, and 7.2. Incubation of a mixture of multicolored nanoparticles with human H2009 lung cancer cells demonstrated sequential activation of the nanoparticles inside endocytic compartments directly correlating with their pH transitions. This multicolored, pH-tunable nanoplatform offers exciting opportunities for the study of many important cell physiological processes, such as pH regulation and endocytic trafficking of subcellular organelles.
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Citations
Cites
Principles of Fluorescence Spectroscopy
Lakowicz, J. R. (1999) · Springer eBooks · doi:10.1007/978-1-4757-3061-6 · Cited by 26,947
Principles of Fluorescence Spectroscopy
(2006) · Springer eBooks · doi:10.1007/978-0-387-46312-4 · Cited by 19,339
Signaling Recognition Events with Fluorescent Sensors and Switches
de Silva, A. P., Gunaratne, H. Q. N., Gunnlaugsson, T., Huxley, A. J. M., McCoy, C. P., Rademacher, J. T., & Rice, T. E. (1997) · Chemical Reviews · doi:10.1021/cr960386p · Cited by 6,995
Alberts, B., Johnson, A., Lewis, J., Raff, M., Roberts, K., & Walter, P. (2007) · W.W. Norton eBooks · doi:10.1201/9780203833445 · Cited by 4,589
Molecular Fluorescence: Principles and Applications
Valeur, B., & Berberan‐Santos, M. N. (2012) · Wiley eBooks · doi:10.1002/9783527650002 · Cited by 4,098
Photoinduced electron transfer in supramolecular systems for artificial photosynthesis
Wasielewski, M. R. (1992) · Chemical Reviews · doi:10.1021/cr00011a005 · Cited by 3,083
The Fluorescent Toolbox for Assessing Protein Location and Function
Giepmans, B. N. G., Adams, S. R., Ellisman, M. H., & Tsien, R. Y. (2006) · Science · doi:10.1126/science.1124618 · Cited by 2,770
Fluorescence Lifetime Measurements and Biological Imaging
Berezin, M. Y., & Achilefu, S. (2010) · Chemical Reviews · doi:10.1021/cr900343z · Cited by 2,403
Stimuli-reponsive polymers and their bioconjugates
GIL, E., & HUDSON, S. (2004) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2004.08.003 · Cited by 2,385
Imaging in the era of molecular oncology
Weissleder, R., & Pittet, M. J. (2008) · Nature · doi:10.1038/nature06917 · Cited by 2,364
Dysregulated pH: a perfect storm for cancer progression
Webb, B. A., Chimenti, M., Jacobson, M. P., & Barber, D. L. (2011) · Nature Reviews Cancer · doi:10.1038/nrc3110 · Cited by 2,237
Sensors and regulators of intracellular pH
Casey, J. R., Grinstein, S., & Orlowski, J. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2820 · Cited by 2,218
New Strategies for Fluorescent Probe Design in Medical Diagnostic Imaging
Kobayashi, H., Ogawa, M., Alford, R., Choyke, P. L., & Urano, Y. (2010) · Chemical Reviews · doi:10.1021/cr900263j · Cited by 2,200
Creating new fluorescent probes for cell biology
Zhang, J., Campbell, R. E., Ting, A. Y., & Tsien, R. Y. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm976 · Cited by 1,981
Micellization of block copolymers
Riess, G. (2003) · Progress in Polymer Science · doi:10.1016/s0079-6700(03)00015-7 · Cited by 1,953
Maxfield, F. R., & McGraw, T. E. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1315 · Cited by 1,729
Activatable Photosensitizers for Imaging and Therapy
Lovell, J. F., Liu, T. W. B., Chen, J., & Zheng, G. (2010) · Chemical Reviews · doi:10.1021/cr900236h · Cited by 1,717
Fluorescent Indicators for Intracellular pH
Han, J., & Burgess, K. (2010) · Chemical Reviews · doi:10.1021/cr900249z · Cited by 1,620
Spectral Absorption and Fluorescence of Dyes in the Molecular State
JELLEY, E. E. (1936) · Nature · doi:10.1038/1381009a0 · Cited by 1,414
Fluorescent probes for super-resolution imaging in living cells
Fernández-Suárez, M., & Ting, A. Y. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2531 · Cited by 1,306
The vacuolar (H+)-ATPases — nature's most versatile proton pumps
Nishi, T., & Forgac, M. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm729 · Cited by 1,197
Selective molecular imaging of viable cancer cells with pH-activatable fluorescence probes
Urano, Y., Asanuma, D., Hama, Y., Koyama, Y., Barrett, T., Kamiya, M., Nagano, T., Watanabe, T., Hasegawa, A., Choyke, P. L., et al. (2009) · Nature Medicine · doi:10.1038/nm.1854 · Cited by 801
A DNA nanomachine that maps spatial and temporal pH changes inside living cells
Modi, S., M. G., S., Goswami, D., Gupta, G. D., Mayor, S., & Krishnan, Y. (2009) · Nature Nanotechnology · doi:10.1038/nnano.2009.83 · Cited by 745
pH-Responsive polymers: synthesis, properties and applications
Dai, S., Ravi, P., & Tam, K. C. (2008) · Soft Matter · doi:10.1039/b714741d · Cited by 693
Zhang, X., Lin, Y., & Gillies, R. J. (2010) · Journal of Nuclear Medicine · doi:10.2967/jnumed.109.068981 · Cited by 659
Fluorescent probes for sensing and imaging
Ueno, T., & Nagano, T. (2011) · Nature Methods · doi:10.1038/nmeth.1663 · Cited by 633
Cellular pH regulators: potentially promising molecular targets for cancer chemotherapy
Izumi, H., Torigoe, T., Ishiguchi, H., Uramoto, H., Yoshida, Y., Tanabe, M., Ise, T., Murakami, T., Yoshida, T., Nomoto, M., et al. (2003) · Cancer Treatment Reviews · doi:10.1016/s0305-7372(03)00106-3 · Cited by 613
Zhou, K., Wang, Y., Huang, X., Luby‐Phelps, K., Sumer, B. D., & Gao, J. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201100884 · Cited by 573
Self-citationThe Dimeric State of Cyanine Dyes
West, W., & Pearce, S. (1965) · The Journal of Physical Chemistry · doi:10.1021/j100890a019 · Cited by 531
Aggregation phenomena in xanthene dyes
Valdes-Aguilera, O., & Neckers, D. C. (1989) · Accounts of Chemical Research · doi:10.1021/ar00161a002 · Cited by 495
Fluorescence probes for critical micelle concentration determination
Goddard, E. D., Turro, N. J., Kuo, P. L., & Ananthapadmanabhan, K. P. (1985) · Langmuir · doi:10.1021/la00063a015 · Cited by 456
Poly(l-histidine)–PEG block copolymer micelles and pH-induced destabilization
Lee, E. S., Shin, H. J., Na, K., & Bae, Y. H. (2003) · Journal of Controlled Release · doi:10.1016/s0168-3659(03)00205-0 · Cited by 451
Kobayashi, H., & Choyke, P. L. (2011) · Accounts of Chemical Research · doi:10.1021/ar1000633 · Cited by 416
Proton-Sponge Coated Quantum Dots for siRNA Delivery and Intracellular Imaging
Yezhelyev, M. V., Qi, L., O’Regan, R. M., Nie, S., & Gao, X. (2008) · Journal of the American Chemical Society · doi:10.1021/ja800086u · Cited by 407
Introduction to Fluorescence Sensing
(2009) · Springer eBooks · doi:10.1007/978-1-4020-9003-5 · Cited by 341
Vogel, S. S., Thaler, C., & Koushik, S. V. (2006) · Science's STKE · doi:10.1126/stke.3312006re2 · Cited by 241
Yu, H., Zou, Y., Wang, Y., Huang, X., Huang, G., Sumer, B. D., Boothman, D. A., & Gao, J. (2011) · ACS Nano · doi:10.1021/nn203503h · Cited by 238
Self-citationGross, S., & Piwnica-Worms, D. (2005) · Cancer Cell · doi:10.1016/j.ccr.2004.12.011 · Cited by 229
Tsien, R. Y. (2003) · PubMed · Cited by 228
Ogawa, M., Kosaka, N., Choyke, P. L., & Kobayashi, H. (2009) · ACS Chemical Biology · doi:10.1021/cb900089j · Cited by 187
Intramolecular Dimers: A New Design Strategy for Fluorescence‐Quenched Probes
Johansson, M. K., & Cook, R. M. (2003) · Chemistry – A European Journal · doi:10.1002/chem.200304941 · Cited by 185
Evaluating Nanoparticle Sensor Design for Intracellular pH Measurements
Benjaminsen, R. V., Sun, H., Henriksen, J. R., Christensen, N. M., Almdal, K., & Andresen, T. L. (2011) · ACS Nano · doi:10.1021/nn201643f · Cited by 168
López Arbeloa, I., & Ruiz Ojeda, P. (1982) · Chemical Physics Letters · doi:10.1016/0009-2614(82)83177-1 · Cited by 162
Activatable imaging probes with amplified fluorescent signals
Lee, S., Park, K., Kim, K., Choi, K., & Kwon, I. C. (2008) · Chemical Communications · doi:10.1039/b806854m · Cited by 149
Delivery and Subcellular Targeting of Dendrimer-Based Fluorescent pH Sensors in Living Cells
Albertazzi, L., Storti, B., Marchetti, L., & Beltram, F. (2010) · Journal of the American Chemical Society · doi:10.1021/ja105689u · Cited by 145
Almutairi, A., Guillaudeu, S. J., Berezin, M. Y., Achilefu, S. A., & Fréchet, J. M. J. (2007) · Journal of the American Chemical Society · doi:10.1021/ja078147e · Cited by 120
Zhou, K., Lu, Y., Li, J., Shen, L., Zhang, G., Xie, Z., & Wu, C. (2008) · Macromolecules · doi:10.1021/ma8019128 · Cited by 103
Self-citationOrganellar Na+/H+ Exchangers: Novel Players in Organelle pH Regulation and Their Emerging Functions
Ohgaki, R., van IJzendoorn, S. C. D., Matsushita, M., Hoekstra, D., & Kanazawa, H. (2010) · Biochemistry · doi:10.1021/bi101082e · Cited by 101
Activatable Molecular Probes for Cancer Imaging
Lee, S., Xie, J., & Chen, X. S. (2010) · Current Topics in Medicinal Chemistry · doi:10.2174/156802610791384270 · Cited by 95
Srikun, D., Albers, A. E., & Chang, C. J. (2011) · Chemical Science · doi:10.1039/c1sc00064k · Cited by 82
Li, C., Xia, J., Wei, X., Yan, H., Si, Z., & Ju, S. (2010) · Advanced Functional Materials · doi:10.1002/adfm.201000038 · Cited by 70
Packard, B. Z., Komoriya, A., Toptygin, D. D., & Brand, L. (1997) · The Journal of Physical Chemistry B · doi:10.1021/jp9702210 · Cited by 49
Cited by
An overview of nanoparticles commonly used in fluorescent bioimaging
Wolfbeis, O. S. (2015) · Chemical Society Reviews · doi:10.1039/c4cs00392f · Cited by 1,631
Diverse Applications of Nanomedicine
Pelaz, B., Alexiou, C., Alvarez-Puebla, R. A., Alves, F., Andrews, A. M., Ashraf, S., Balogh, L. P., Ballerini, L., Bestetti, A., Brendel, C., et al. (2017) · ACS Nano · doi:10.1021/acsnano.6b06040 · Cited by 1,350
Ge, Z., & Liu, S. (2013) · Chemical Society Reviews · doi:10.1039/c3cs60048c · Cited by 914
Wang, Y., Zhou, K., Huang, G., Hensley, C., Huang, X., Ma, X., Zhao, T., Sumer, B. D., DeBerardinis, R. J., & Gao, J. (2014) · Nature Materials · doi:10.1038/nmat3819 · Cited by 773
Self-citationOptical Sensing and Imaging of pH Values: Spectroscopies, Materials, and Applications
Steinegger, A., Wolfbeis, O. S., & Borisov, S. M. (2020) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00451 · Cited by 622
Metadata
- Authors
- Zhou, K., Liu, H., Zhang, S., Huang, X., Wang, Y., Huang, G., Sumer, B. D., & Gao, J.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2012-04-24
- Volume
- 134
- Issue
- 18
- Pages
- 7803-7811
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2101902313
- Cited by
- 344
- References
- 52
- FWCI
- 14.48
- Type
- journal article
- Language
- en
- Open access
- green
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