一種用于活細(xì)胞中檢測(cè)Zn2+的萘酚席夫堿類熒光探針

陳 邦 王少靜 宋戰(zhàn)科 郭 媛

一種用于活細(xì)胞中檢測(cè)Zn2+的萘酚席夫堿類熒光探針

陳 邦 王少靜 宋戰(zhàn)科 郭 媛＊

(西北大學(xué)化學(xué)與材料科學(xué)學(xué)院，合成與天然功能分子化學(xué)教育部重點(diǎn)實(shí)驗(yàn)室，西安 710127)

設(shè)計(jì)合成了1種基于C=N異構(gòu)化和螯合熒光增強(qiáng)機(jī)理 (CHEF)的Zn2+熒光探針BMO和NBMO，其結(jié)構(gòu)經(jīng)1H NMR，13C NMR，1H-1H COSY，HSQC，IR和HRMS進(jìn)行了表征。光譜分析實(shí)驗(yàn)結(jié)果顯示，探針對(duì)Zn2+均具有較好的選擇性和靈敏度，檢出限分別為30和21 nmol·L-1。在0～20μmol·L-1濃度的范圍內(nèi)，BMO和NBMO的熒光強(qiáng)度與Zn2+濃度可呈良好的線性關(guān)系。NBMOZn2+配合物單晶結(jié)構(gòu)和Job曲線證實(shí)該探針與Zn2+以1∶1配位。NBMO被成功應(yīng)用于活細(xì)胞中Zn2+的檢測(cè)。

熒光探針；C=N異構(gòu)化；螯合熒光增強(qiáng)；鋅離子；活細(xì)胞成像

Zn2+is the second most abundant trace essential metals in the human body after iron and plays a critical role in many biochemical and physiological processes such as protein metabolism,reproduction,cell growth,cell division,cellular transport,immune system,and gene transcription[1-3].Importantly,deficiency or excess of this essential trace element is known to have adverse consequences to human health[4].Any disruption in the bio-availability of Zn2+in the mammalian system may cause serious diseases such as Alzheimer′s,amyotrophic lateral sclerosis(ALS),Parkinson′s,ischemia,epilepsy[5],while excess accumula-tion of Zn2+in human body may lead to health hazards.Thus,spatiotemporal detection of Zn2+in biological samples is of great significance for understanding the role of Zn2+in biology.

Consequently,more and more researchers focus on the study of detection methods for Zn2+.The topical detection methods include atomic absorption spectrometry(AAS)[6],atomic emission spectrometry(AES)[7],electrochemical method[8]and fluorescent sensors,wherein fluorescent probes have attracted enormous interest because of their high sensitivity,operational simplicity and instantaneous response[9-22].Up to now,a number of fluorescent probes for detecting Zn2+have been designed based on rhodamine[23],coumarin[24],quinolone[25],fluorescein[26]and BODIPY[27].They have good binding affinity with Zn2+.However,there still exists some drawbacks among the reported fluorescence probes,e.g.the detection limit of probes is restricted[28], some of the sensors are hard to synthesize[29],and optical properties are interfered from other metal ions,such as Cd2+which exhibits highly similar chemical properties as Zn2+[30].Therefore,to develop the Zn2+fluorescence probes with low detection limit,high selectivity and high sensitivity are expected to remain challenging.

Over the past few decades,various Zn2+fluorescence probes have been designed and synthesized to address the above challenge,wherein the probes based on C=N isomerization mechanism have outstanding performance and attracted extensive attention.As we know,the fluorescence probe containing C=N double bond with a lone electron pair has good ability to coordinate with metal ions.Compounds with an unbridged C=N structure are often nonfluorescent due to the C=N isomerization.In contrast,complexation with metal ions restricts the rotation of the C=N bond and produces a chelation-enhanced fluorescence(CHEF)effect.Based on the mechanism,we report two novel Zn2+fluorescence probes(BMO and NBMO)herein.Studies show that BMO and NBMO are highly selectivity for Zn2+over its family Cd2+and the other metal ions.The X-ray crystal structure of the NBMOZn2+complex exposes its coordination feature and the Job plots reveal a 1∶1 probe-Zn2+identification.Moreover,the cell images show that NBMO can be used to detect intracellular Zn2+.

1 Experimental

1.1 Reagent and apparatus

Unless otherwise stated,all reagents were purchased from commercial suppliers and used without further purification.A549 cells were purchased from the Committee on type Culture Collection of Chinese Academy of Sciences.NMR spectra were collected on a Varian INOVA-400 spectrometer 400 MHz for1H NMR and 100 MHz for13C NMR.High-resolution mass spectra(HRMS)were obtained with an Ulti Mate 3000 Mass Spectrophotometer.FT-IR spectra were obtained in KBr pellets on a Bruker EQUIOX-55 FTIR spectrometer.The single crystal structure was determined by a Bruker Smart ApexIICCD X-ray crystallography.Absorption spectra were recorded on a UV-1700 spectrophotometer.Fluorescent spectra were recorded on a Hitachi F-4500 fluorescence spectrophotometer.Cell imaging was observed under a confocal laser scanning microscope(Olympus FV1000)with excitation at 405 nm.

1.2 Sample preparation and measurements

Stock solutions(1 mmol·L-1)of BMO and NBMO were prepared in DMSO.Stock solutions(10 mmol·L-1)of the chloride salts of Cd2+,Ca2+,Mg2+,Mn2+,Hg2+,Fe3+,Al3+,Cr3+,Co2+,Ni2+,Cu2+and Zn2+metal ions and acetate salts of Pb2+and Ag+metal ions were prepared in fresh deionized water.The spectra changes of BMO and NBMO towards Zn2+were evaluated in Tris-HCl buffer solution(10 mmol·L-1,pH=7.4)containing 20%DMSO.Unless otherwise noted,for all the measurements,the excitation wavelength was at 376 nm,the excitation slit was at 10 nm,and the emission slit was at 10 nm.

1.3 Synthesis of BMO and NBMO

Scheme 1 Synthesis of BMO and NBMO

Synthesis of 1H-benzimidazole-2-methanamine(1):amino acetic acid(0.9 g,12 mmol)and o-Phenylenediamine (1.08 g,10 mmol)were dissolved in 6 mol·L-1HCl(14 mL).The reaction mixture was stirred at 120℃for two days.After being cooled to room temperature,the pH of the reaction liquid was adjusted to 7～8 with strong aqua ammonia,then the mixture was frozen till the solid no longer formation.The solid was collected and recrystallized by distilled water to afford the desired product as colorless needle-like crystals.1H NMR(400 MHz,DMSO-d6):δ2.03(br,2H),3.91(s,2H),7.10～7.12(m,2H),7.47～7.49(m,2H).

Synthesis of 1-methyl-1H-benzimidazole-2-methanamine(2):N-methyl-o-phenylenediamine(1.22 g,10 mmol)and amino acetic acid (0.9 g,12 mmol)were dissolved in 6 mol·L-1HCl(14 mL).The reaction mixture was stirred at 120℃for two days.After being cooled to room temperature,the pH of the reaction liquid was adjusted to 7～8 with strong aqua ammonia,then the mixture was frozen till the solid no longer formation.The solid was collected and recrystallized by distilled water to afford the desired product as light pink needle-like crystals.1H NMR(400 MHz,DMSO-d6):δ1.93(br,2H),3.78(s,5H),3.95(s,4H),7.13～7.22(m,2H),7.50(d,J=7.8 Hz,1H),7.56(d,J=7.7 Hz,1H);13C NMR (100 MHz,DMSO-d6):δ161.31,147.05,141.24,126.76,126.27,123.63,114.86,43.63,34.62;HRMS(ESI):m/z,Calcd.for C9H11N3[M+H]+162.1031;Found 162.103 0.

Synthesis of BMO:2-hydroxy-1-naphthaldehyde(0.86 g,5 mmol)and compound 1(0.88 g,6 mmol)were dissolved in 15 mL anhydrous methanol.The reaction mixture was stirred at room temperature for 5 h.The precipitated was filtered,washed with cold methanol,and dried in vacuum to afford the desired product as a yellow solid.(1.38 g,yield:92%).1H NMR(400 MHz,DMSO-d6):δ5.14 (s,2H),6.83 (d,J=9.1 Hz,1H),7.18～7.28(m,3H),7.48～7.55(m,3H),7.71(d,J=7.5 Hz,1H,),7.81(d,J=9.2 Hz,1H),8.17(d,J=8.2 Hz,1H),9.42(d,J=7.8 Hz,1H,),12.60(s,1H),14.37(s,1H);13C NMR (100 MHz,DMSO-d6):δ174.50,161.74,151.28,137.29,134.33,129.42,128.44,126.25,124.50,123.11,122.74,121.82,119.39,119.16,111.82,107.20,50.83;FT-IR(KBr,cm-1):3 446,3 014,2 924,2 739,1 750,1 629,1 546,1 432,1 359,1 319,1 267,1 190,1 145,1 032,990,837,745,621;HRMS(ESI):m/z,Calcd.for C19H15N3O[M+H]+302.129 3;Found 302.126 8.

Synthesis of NBMO:To a mixture 2-hydroxy-1-naphthaldehyde (0.86 g,5 mmol)and compound 2(0.97 g,6 mmol)was added anhydrous methanol(15 mL).The mixture was stirred at room temperature for 5 h.The precipitated was filtered,washed with cold methanol,and dried in vacuum to afford the desired product as a yellow-green solid (1.46 g,yield:94%).1H NMR(400 MHz,DMSO-d6):δ3.38(s,3H),5.24(s,2H),6.82(d,J=8 Hz,1H),7.19～7.29(m,3H),7.45～7.66(m,3H),7.71(d,J=7.8 Hz,1H),7.81(d,J=9.3 Hz,1H),8.15(d,J=8.3 Hz,1H),9.45(d,J=8.1 Hz,1H),14.40(s,1H);13CNMR(100 MHz,DMSO-d6):δ174.63,161.45,151.35,142.43,137.31,136.45,134.30,129.43,128.48,126.23,124.56,123.12,122.72,122.11,119.30,110.62,107.18,99.98,49.09,30.24;FT-IR(KBr,cm-1):3 677,3 420,3 029,2 917,1 622,1 537,1 466,1 426,1 398,1 350,1 313,1 259,1 188,1 142,1 060,1 032,995,905,844,741;HRMS(ESI):m/z,Calcd.for C20H17N3O[M+H]+316.145 0;Found 316.143 0.

1.4 X-crystallographic analysis

Fig.1 (a)X-ray crystal structures of NBMO-Zn2+complex and(b)packing arrangement for NBMO-Zn2+

Single crystals suitable for X-ray diffraction were prepared by slow evaporation of a solution of NBMO/ZnCl2in methanol at room temperature.The single crystal X-ray structure and packing diagram of the NBMO-Zn2+complex are shown in Fig.1.NBMO and Zn2+ion formed a 1∶1 stoichiometry.Single-crystal X-ray diffraction data was collected on a Bruker Smart Ape II CCD X-ray diffractometer.The structure was solved by direct methods and refined by full matrix least-square on F2using the SHELXTL-97 program[31].All non-hydrogen atoms were refined anisotropically.All the H atoms were positioned geometrically and refined using a riding model.The details of the crystal parameters,data collection,and refinements for complex NBMO-Zn2+were listed in Table S1.Selected bond lengths and bond angles were listed in Table S2 and Table S3 respectively.

CCDC:1558816.

1.5 Intracelluar Zn2+imaging with NBMO

A549 cells were cultured in Roswell Park Memorial Institute 1640 (RPMI 1640)supplemented with 10%(V/V)fetal bovine serum(FBS),100 units per mL of penicillin and 100 units per mL of streptomycin at 37℃in a CO2incubator.The A549 cells were incubated with 20 μmol·L-1of probe NBMO for 30 min at 37 ℃.Then pretreated with 60 μmol·L-1Zn2+for 30 min at 37 ℃ and after added with 1 μmol·L-1TPEN(N,N,N′,N′-tetrakis(2-pyridylmethyl)-ethylenediamine)for 30 min at 37℃.The cells were washed three times with PBS buffer before cell fluorescence imaging experiments with confocal laser scanning microscopy[32].

2 Results and discussion

To get insight into fluorescence intensity changes with an increase of Zn2+concentration,the fluorescence spectra changes of BMO and NBMO towards Zn2+were evaluated.As shown in Fig.2,upon the addition of Zn2+to the solution of BMO or NBMO,the emission intensity at 450 nm clearly increased.Moreover,there was a good linear relationship between the fluorescence intensity of probes (BMO and NBMO)and the concentration of Zn2+in the range of 0 to 20 μmol·L-1(Inset in Fig.2).According to the reported definition(S/N=3),the detection limit of BMO and NBMO for Zn2+were found to be 30 and 21 nmol·L-1respectively.The results prove that NBMO has a higher sensitivity toward Zn2+than BMO.

Fig.2 Fluorescence changes of(a)BMOand(b)NBMO(20 μmol·L-1)with different concentrations of Zn2+(0～20 μmol·L-1)in buffer solution with an excitation at 376 nm

The binding constants K of BMO-Zn2+and NBMO-Zn2+were calculated by the Benesi-Hildebrand equation.Depending on the slope,the results obtained were KBMO=4.96×104L·mol-1and KNBMO=3.25×104L·mol-1,signifying that BMO and NBMO had a great binding affinity to Zn2+(Fig.S17). In order to further study the binding of probes with Zn2+,the Job plots were tested by using a total concentration of 20μmol·L-1probe and Zn2+,and the results indicate that the combination of probes and Zn2+is 1∶1 stoichiometry(Fig.3).

The kinetic studies were conducted by monitoring the fluorescence intensity changes of BMO and NBMO at 450 nm in the presence of Zn2+.The results show that the chelation process can be completed within 30 s (Fig.4).The pH value of the system is often considered as a significant factor for the properties of fluorescent probe.The effect of pH on the fluorescence response of BMO and NBMO to Zn2+ions was studied by adjusting the pH value ranging from 3.0 to 9.0.As shown in Fig.5,no noticeable fluorescence emission of pure BMO and NBMO were observed in a wide range of pH values.Upon the addition of Zn2+,a significant increase in the fluorescence intensity were observed in the range of 4.0 to 9.0,which clearly indicated the compatibility of BMO and NBMO for biological applications under physiological conditions.

To further understand the fluorescent properties of BMOand NBMOwith Zn2+,thefluorescenceresponse behavior of BMO and NBMO to various metal ions was systematically investigated(Fig.6).As expected,there were no obvious changes in the fluorescence intensity after adding other metal ions to BMO and NBMO solution,including Cd2+,Ca2+,Mg2+,Pb2+,Mn2+,Hg2+,Ag+,Fe3+,Al3+and Cr3+.However,the presence of Co2+,Ni2+and Cu2+quench the fluorescence possibly because of the heavy metal effect.Moreover,the competitive experiments confirmed that the presence of metal ions,such as Cd2+,Ca2+,Mg2+,Pb2+,Mn2+,Hg2+,Ag+,Fe3+and Al3+,did not interfere with the enhanced fluorescence (Fig.7).However,the presence of Cr3+would seriously weaken the enhanced fluorescence and Co2+,Ni2+and Cu2+totally quenched the fluorescence,possibly because the complex formed between these metals and the probes was too stable to be replaced by Zn2+.These results indicate that BMO and NBMO,have good selectivity toward Zn2+,which facil-itates the accurate detection under complex biosystem.

Fig.3 Job plots of(a)BMO-Zn2+and(b)NBMO-Zn2+

Fig.4 Time-course fluorescence response spectra of(a)BMO and(b)NBMO(20 μmol·L-1)towards Zn2+(60 μmol·L-1)

Fig.5 Effect of pH value on the fluorescence intensity of(a)BMO and(b)NBMO(20 μmol·L-1)upon the addition of Zn2+(20 μmol·L-1)

Fig.6 Fluorescence emission spectra of(a)BMOand(b)NBMO(20 μmol·L-1)in the presence of different ions such as Cd2+,Ca2+,Mg2+,Pb2+,Mn2+,Hg2+,Ag+,Fe3+,Al3+,Cr3+,Co2+,Ni2+,Cu2+and Zn2+in Tris-HCl buffer(10 mmol·L-1,pH=7.4)

Fig.7 Metal ion selectivity of(a)BMOand(b)NBMO(20 μmol·L-1)in Tris-HCl buffer(10 mmol·L-1,pH=7.4);Concentration of Zn2+was 20 μmol·L-1,and that of the other metal ions 40 μmol·L-1.Black bars represent the addition of the appropriate metal ions to the solution of BMOor NBMO.Red bars represent the subsequent addition of Zn2+to the solution

On the basis of the fluorescence response of BMO and NBMO toward Zn2+,the recognition mechanism is proposed as shown in Fig.8.The weak fluorescence of BMO and NBMO are due to the free rotation around C=N bond.In contrast,complexation with Zn2+inhibits the rotation of the C=N bond and produces a chelationenhanced fluorescence(CHEF)effect.To confirm the supposed recognition mechanism,1H NMR titration experiment was carried out in DMSO-d6/D2O.Fig.9(a)shows1H NMR spectrum of NBMO.The peaks at 14.43 and 9.45 were assigned to-OH(Ha)and-CH=N-(Hb)of NBMO,respectively.Fig.9(b)shows the1H NMR spectra of NBMO upon the addition of Zn2+with 3.0 equiv.concentrations.It was clearly found that the peak of Haat 14.43 disappeared,demonstrating that-OH(Ha) was involvs in the complexation of Zn2+and NBMO.The peak shape of-CH=N-(Hb)was changed from double peak to single peak after complexation,which further proved inhibition of the rotation of the C=N bond in the complex molecule.The1H NMR titration result supports the binding of Zn2+with NBMO through a chelation reaction via phenolic-O atoms and the imine-N atoms.

The aforementioned favorable properties of BMO and NBMO in chemical system encouraged us to investigate their practical utilities in living cells.Taking into account the better spectral properties of NBMO,application of NBMO for cellular imaging was measured using A549 cells.Prior to being applied in cell imaging,MTT assay was first performed to assess its biocompatibility.Cytotoxicity experiments demonstrated minimal cytotoxicity of NBMO toward A549 cells at 25 μmol·L-1(80% viability,Fig.S18).Next,we further investigated its potential utility for the detection of Zn2+in living cells by using the confocal fluorescence microscope.As shown in Fig.10,the A549 cells displayed the weakly fluorescence after incubated with the probe NBMO for 30 min at 37℃.After addition of Zn2+for 10 min at 37℃,the fluorescence clearly increased,indicating that the NBMO could combine Zn2+to form complex NBMOZn2+and then enhance the fluore-scence intensity.After following addition TPEN for 10 min at 37℃,the strong fluorescence was decreased greatly.Thus,above results clearly document the applicability of NBMO as a fluorescent probe to detect intracellular Zn2+ions.

Fig.8 Recognition mechanism of BMO and NBMO to Zn2+

Fig.9 1H NMR spectra in DMSO-d6/D2Oof(a)NBMO only,(b)NBMO with 3.0 equiv.of Zn2+

Fig.10 (a)First row:Images of living A549 cells incubated with NBMO(20 μmol·L-1)for 30 min;the second row:Images of living A549 cells incubated with NBMO(20 μmol·L-1)for 30 min,and further incubated with Zn2+(60 μmol·L-1)for 10 min;the third row:Images of living A549 cells incubated with NBMO(20 μmol·L-1)for 30 min,and further incubated with Zn2+(60 μmol·L-1)for 10 min,then incubated with TPEN(1 μmol·L-1)for 10 min;(b)Relative pixel intensity of fluorescence images row 1,2 and 3

3 Conclusions

We have successfully developed two novel probes,BMO and NBMO,as efficient chemical sensors for the highly selective detection of Zn2+in aqueous media.Towards this aim,the two probes were designed and synthesized through a simple condensation of 2-aminomethylbenzimidazole derivatives and 2-hydroxy-1-naphthaldehyde based on C=N isomerization and chelation-enhanced fluorescence (CHEF)mechanism.Their kinetic study towards Zn2+displayed a fast response time (both less than 30 s).Selective and competitive experiments were performed to exhibit an excellent selectivity of Zn2+ions over its family Cd2+and other metal ions.Moreover,the detection limit of BMO and NBMO were found to be 30 nmol·L-1and 21 nmol·L-1respectively,which exhibited an excellent sensitivity of the two probes.Meanwhile,NBMO has been used to image intracellular Zn2+ions in living A549 cells with a good performance.

Supporting information isavailable at http://www.wjhxxb.cn

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Naphthol-Based Shiff Base as a Selective Fluorescent Probe for Detecting Zn2+in Living Cells

Two fluorescent probes BMO and NBMO were developed for the highly selective detection of Zn2+based on C=N isomerization and chelation-enhanced fluorescence (CHEF)mechanism.Structure identification of the probes was confirmed by1H NMR,13CNMR,1H-1H COSY,HSQC,IR and HRMSspectroscopy.The results of spectral analysis show that BMO and NBMO are sensitive and highly selective to Zn2+.The detection limit of BMO and NBMO are found to be 30 and 21 nmol·L-1respectively.There is a good linear relationship between the fluorescence intensity of probes (BMO and NBMO)and the concentration of Zn2+in the range of 0 to 20 μmol·L-1.The X-ray crystal structure of the NBMO-Zn2+complex exposes its coordination feature and the Job plots reveal a 1∶1 probe-Zn2+identification.Thecell imagesshow that NBMOcan beused to detect intracellular Zn2+.

fluorescent probe;C=N isomerization;chelation-enhanced fluorescence;zinc ion;living cell imaging

O626.23

A

1001-4861(2017)10-1722-09

10.11862/CJIC.2017.227

CHEN Bang WANG Shao-Jing SONG Zhan-Ke GUOYuan＊
(Key Laboratory of Synthetic and Natural Functional Molecular Chemistry of Ministry of Education,College of Chemistry and Materials Science,Northwest University,Xi′an 710127,China)

2017-05-23。收修改稿日期：2017-09-01。

國(guó)家自然科學(xué)基金(No.21472148，21072158)，陜西省留學(xué)人員科技活動(dòng)擇優(yōu)資助項(xiàng)目(No.20151190)和西北大學(xué)優(yōu)秀青年學(xué)術(shù)骨干支持計(jì)劃資助。

＊通信聯(lián)系人。 E-mail：guoyuan@nwu.edu.cn