摘要
Fluorescence imaging has facilitated fluorescent probes to analyze the subcellular localization and dynamics of biological targets. In this paper, we reported a fluorogenic probe for bacteria imaging. The probe was an imidazolium-derived pyrene compound, which self-assembled to form nano-particles and the pyrene fluorescence was quenched by the aggregation effects. When the self-assembly nanoparticles interacted with anionic bacteria surfaces, synergistic effects of electrostatic interaction and hydrophobic force caused competing binding between bacteria surfaces and imidazoliums. This binding resulted in the disassembly of the aggregates to give fluorescence turn-on signal. Meanwhile, the probe bound bacteria surfaces and displayed both pyrene-excimer and pyrene-monomer fluorescence, which gave ratiometric signal. Then, fluorescent labeling by the probe enabled the two-photo ratiometric imaging of bacteria.
Fluorescence imaging has facilitated fluorescent probes to analyze the subcellular localization and dynamics of biological targets. In this paper, we reported a fluorogenic probe for bacteria imaging. The probe was an imidazolium-derived pyrene compound, which self-assembled to form nano-particles and the pyrene fluorescence was quenched by the aggregation effects. When the self-assembly nanoparticles interacted with anionic bacteria surfaces, synergistic effects of electrostatic interaction and hydrophobic force caused competing binding between bacteria surfaces and imidazoliums. This binding resulted in the disassembly of the aggregates to give fluorescence turn-on signal. Meanwhile, the probe bound bacteria surfaces and displayed both pyrene-excimer and pyrene-monomer fluorescence, which gave ratiometric signal. Then, fluorescent labeling by the probe enabled the two-photo ratiometric imaging of bacteria.
引文
[1]K.E. Jones, N.G. Patel, M.A. Levy, et al., Nature 451(2008)990-993.
[2]P.C. Ray, S.A. Khan, A.K. Singh, et al., Chem. Soc. Rev. 41(2012)3193-3209.
[3]D.J. Payne, M.N. Gwynn, D.J. Holmes, et al., Nat. Rev. Drug Discov. 6(2007)29-40.
[4]R. Chauvet, F. Lagarde, T. Charrier, et al., Appl. Spectrosc. Rew. 52(2017)123-144.
[5]M. Welker, Proteomics 11(2011)3143-3153.
[6](a)J.D. Wang, X.H. Wang, Y. Li, et al., Anal. Sci. 28(2012)237-241;(b)S.M. Hossain, C. Ozimok, C.Sicard, et al., Anal. Bioanal. Chem. 403(2012)1567-1576.
[7](a)R.L.Phillips, O.R. Miranda, CC. You, et al., Angew. Chem. Int. Ed. 47(2008)590-2594;(b)J. Han, H. Cheng, B. Wang, et al., Angew. Chem. Int. Ed. 56(2017)15246-15251;(c)W.Chen, Q. Li, W.Zheng, et al., Angew. Chem. Int. Ed. 53(2014)13734-13739.
[8](a)S. Leng, Q. Qiao, Y. Gao, et al., Chin. Chem. Lett. 28(2017)1911-1915;(b)L. Peng, Y. Xu, P. Zou, Chin. Chem. Lett. 28(2017)1925-1928;(c)Z. Xu, J. Chen, L.Hu, et al.,Chin. Chem. Lett. 28(2017)1935-1942;(d)P. Ning, W.Wang, M. Chen, et al.,Chin. Chem. Lett. 28(2017)1943-1951;(e)D. Wu, Y. Shen, J. Chen, et al.,Chin. Chem. Lett. 28(2017)1979-1982.
[9](a)E. Zhao, Y. Chen, S. Chen, et al.,Adv. Mater. 27(2015)4931-4937;(b)T. Gao, X. Cao, J. Dong, et al.,Dyes Pigm. 143(2017)436-443;(c)Y. Li, X. Liu, X. Yang, et al., ACS Nano 11(2017)10672-10680.
[10]N. Geva-Zatorsky, D. Alvarez,J.E. Hudak, et al., Nat. Med. 21(2015)1091-1100.
[11]S. Peyton, M.S. Siegrist, A.J. Cullen, et al., Proc.Natl. Acad. Sci. U. S. A. 111(2014)5456-5461.
[12]R.L Strack, W.Song, S.R. Jaffrey, Nat. Protocol. 9(2014)146-155.
[13]Z. Xu, N.J. Singh, J. Lim, et al., J. Am. Chem. Soc. 131(2009)15528-15533.
[14]Z. Li, Y. Li, D. Wang, et al.,Chin. Chem. Lett 29(2018)1645-1647.
[15]Z. Xu, S.K. Kim, J. Yoon, Chem. Soc. Rev. 39(2010)1457-1466.
[16]Z. Xu, N.J. Singh, J. Lim, et al., J. Am. Chem. Soc.131(2009)15528-15533.
[17]Z. Xu, D.R. Spring, J. Yoon, Chem. Asian J. 6(2011)2114-2122.
[18]Z. Xu, J.Y. Choi, J. Yoon, Bull. Korean Chem. Soc. 32(2011)1371-1374.