A thiol fluorescent probe containing SNAP-tagTM substrate

  • LIN Lixia ,
  • GUO Chunqing ,
  • WANG Libin ,
  • ZHAO Zibiao ,
  • XIONG Kangming
Expand
  • 1. Department of Security, Shanxi Police College, Taiyuan 030401, China; 2. Key Laboratory of Nano-imaging and Drugloaded Preparation of Shanxi Province, Shanxi Bethune Hospital, Taiyuan 030032, China; 3. CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China

Received date: 2023-06-15

  Online published: 2024-09-25

Abstract

A coumarin-based probe coumarin-alkene ketone-benzylaminoguanine(CAKBG)containing both α, β-unsaturated ketone and SNAP-tagTM substrate was synthesized. By testing the UV-Vis absorption spectra and fluorescence emission spectra of the probe CAKBG, the results show that the probe CAKBG has a longer absorption wavelength in polar solvents( such as glycerol, ethylene glycol, water, DMSO), and the probe CAKBG is not sensitive to the pH change of the solutions. In addition, spectral experiments show that both Cys and Hcy can cause a blue shift in the maximum absorption wavelength of the probe CAKBG, and when the excitation wavelength is 405 nm, both Cys and Hcy can cause the fluorescence emission peak of the probe CAKBG at 487 nm to be significantly enhanced. Cell imaging results show that the thiol fluorescent probe CAKBG containing SNAP-tagTM substrate can image Cys and Hcy in living cells. The above results indicate that SNAP-TagTM protein labeling technology is expected to be widely- DOI:10.3969/j.issn.1000-1565.2024.05.007一种含SNAP-tagTM底物的硫醇荧光探针林利霞1,郭春青1,王利斌1,赵子彪1,熊康明2,3(1.山西警察学院 治安系,山西 太原 030401;2.山西白求恩医院 纳米成像与载药制剂山西省重点实验室,山西 太原 030032;3.中国科学院大连化学物理研究所 分离分析化学重点实验室,辽宁 大连 116023)摘 要:合成了一种同时含α, β-不饱和酮活性位点和SNAP-tagTM底物的香豆素母体探针香豆素-烯酮-苯甲氨基鸟嘌呤(CAKBG).通过测试探针CAKBG的紫外-可见吸收光谱和荧光发射光谱,发现探针CAKBG在极性溶剂(例如, 甘油、乙二醇、水、DMSO)中有更长的吸收波长,且探针CAKBG对溶液的pH变化不敏感.此外,光谱实验发现生物硫醇Cys和Hcy均能引起探针CAKBG的最大吸收波长发生蓝移,且当激发波长为405 nm时,Cys和Hcy均能导致探针CAKBG在487 nm处的荧光发射峰明显增强.细胞成像结果表明,含有SNAP-tagTM底物的硫醇荧光探针CAKBG在活细胞中可以对Cys、Hcy进行荧光成像.综上,SNAP-TagTM蛋白标签技术有望今后在硫醇荧光探针的细胞成像中得到推广应用.关键词:α, β-不饱和酮;SNAP-TagTM底物;硫醇荧光探针;细胞成像中图分类号:O622.4 文献标志码:A 文章编号:1000-1565(2024)05-0504-09A thiol fluorescent probe containing SNAP-tagTM substrateLIN Lixia1, GUO Chunqing1, WANG Libin1, ZHAO Zibiao1, XIONG Kangming2,3(1. Department of Security, Shanxi Police College, Taiyuan 030401, China; 2. Key Laboratory of Nano-imaging and Drugloaded Preparation of Shanxi Province, Shanxi Bethune Hospital, Taiyuan 030032, China; 3. CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China)Abstract: A coumarin-based probe coumarin-alkene ketone-benzylaminoguanine(CAKBG)containing both α, β-unsaturated ketone and SNAP-tagTM substrate was synthesized. By testing the UV-Vis absorption spectra and fluorescence emission spectra of the probe CAKBG, the results show that the probe CAKBG has a longer absorption wavelength in polar solvents( such as glycerol, ethylene glycol, water, DMSO), and the probe CAKBG is not sensitive to the pH change of the solutions. In addition, spectral experiments show that both Cys and Hcy can cause a blue shift in the maximum absorption wavelength of the probe CAKBG, and when the excitation wavelength is 405 nm, both Cys and Hcy can cause the fluorescence emission peak of the probe CAKBG at 487 nm to be significantly enhanced. Cell imaging results show that the thiol fluorescent probe CAKBG containing SNAP-tagTM substrate can image Cys and Hcy in living cells. The above results indicate that SNAP-TagTM protein labeling technology is expected to be widely- 收稿日期:2023-06-15;修回日期:2023-09-12 基金项目:国家自然科学基金资助项目(22008232);山西省基础研究计划青年科学研究项目(202203021212512) 第一作者:林利霞(1991—),女,山西警察学院讲师,博士,主要从事有机小分子的光谱性能研究. E-mail:1552774577@qq.com 通信作者:熊康明(1990—),男,山西白求恩医院副研究员,博士,主要从事荧光探针的传感识别研究. E-mail:1187994460@qq.com 第5期林利霞等:一种含SNAP-tagTM底物的硫醇荧光探针河北大学学报(自然科学版) 第44卷used in cell imaging of thiol fluorescent probes in the future.

Cite this article

LIN Lixia , GUO Chunqing , WANG Libin , ZHAO Zibiao , XIONG Kangming . A thiol fluorescent probe containing SNAP-tagTM substrate[J]. Journal of Hebei University(Natural Science Edition), 2024 , 44(5) : 504 -512 . DOI: 10.3969/j.issn.1000-1565.2024.05.007

References

[1] SHAHROKHIAN S. Lead phthalocyanine as a selective carrier for preparation of a cysteine-selective electrode[J]. Anal Chem, 2001, 73(24): 5972-5978. DOI: 10.1021/ac010541m.
[2] SESHADRI S, BEISER A, SELHUB J, et al. Plasma homocysteine as a risk factor for dementia and Alzheimer’s disease[J]. N Engl J Med, 2002, 346(7): 476-483. DOI: 10.1056/NEJMoa011613.
[3] DALTON T P, SHERTZER H G, PUGA A. Regulation of gene expression by reactive oxygen[J]. Annu Rev Pharmacol Toxicol, 1999, 39: 67-101. DOI: 10.1146/annurev.pharmtox.39.1.67.
[4] VACEK J, KLEJDUS B, PETRLOVÁ J, et al. A hydrophilic interaction chromatography coupled to a mass spectrometry for the determination of glutathione in plant somatic embryos[J]. Analyst, 2006, 131(10): 1167-1174. DOI: 10.1039/b606432a.
[5] LIANG G L, RONALD J, CHEN Y X, et al. Controlled self-assembling of gadolinium nanoparticles as “smart” molecular magnetic resonance imaging contrast agents[J]. Angew Chem Int Ed Engl, 2011, 50(28): 6283-6286. DOI: 10.1002/anie.201007018.
[6] KACZYÑSKA A, PELSERS M M A L, BOCHOWICZ A, et al. Plasma heart-type fatty acid binding protein is superior to troponin and myoglobin for rapid risk stratification in acute pulmonary embolism[J]. Clin Chim Acta, 2006, 371(1/2): 117-123. DOI: 10.1016/j.cca.2006.02.032.
[7] MACCOSS M J, FUKAGAWA N K, MATTHEWS D E. Measurement of homocysteine concentrations and stable isotope tracer enrichments in human plasma[J]. Anal Chem, 1999, 71(20): 4527-4533. DOI: 10.1021/ac990541a.
[8] WANG Y T, YAN H M, YUE Y K, et al. GSH and H2O2 dynamic correlation in the ferroptosis pathways revealed by engineered probe in tumor and kidney injury[J]. Chem Eng J, 2023, 464: 142496. DOI: 10.1016/j.cej.2023.142496.
[9] 孟美荣,阴彩霞.一种荧光增强型的GSH荧光探针[J].河北大学学报(自然科学版), 2019, 39(1): 49-55. DOI: 10.3969/j.issn.1000-1565.2019.01.009.
[10] LIU Y, WU Y X, ZHANG D L, et al. Rational design of in situ localization solid-state fluorescence probe for bio-imaging of intracellular endogenous cysteine[J]. Talanta, 2020, 220: 121364. DOI: 10.1016/j.talanta.2020.121364.
[11] CHEN J, LI Y W, FENG X K, et al. An ICT-based fluorescent probe guided by theoretical calculation for selectively mapping endogenous GSH in living cells[J]. Spectrochim Acta A Mol Biomol Spectrosc, 2021, 246: 119041. DOI: 10.1016/j.saa.2020.119041.
[12] CAI S T, LIU C, JIAO X J, et al. A lysosome-targeted near-infrared fluorescent probe for imaging endogenous cysteine(Cys)in living cells[J]. J Mater Chem B, 2020, 8(11): 2269-2274. DOI: 10.1039/C9TB02609F.
[13] HE R K, ZHANG Y C, MADHU S, et al. BODIPY based realtime, reversible and targeted fluorescent probes for biothiol imaging in living cells[J]. Chem Commun, 2020, 56(93): 14717-14720. DOI: 10.1039/d0cc06313d.
[14] ZHU Y D, PAN H T, SONG Y Y, et al. Mitochondria-targeted fluorescent probe for rapid detection of thiols and its application in bioimaging[J]. Dyes Pigm, 2021, 191: 109376. DOI: 10.1016/j.dyepig.2021.109376.
[15] LIANG B B, WANG B Y, MA Q J, et al. A lysosome-targetable turn-on fluorescent probe for the detection of thiols in living cells based on a 1, 8-naphthalimide derivative[J]. Spectrochim Acta A Mol Biomol Spectrosc, 2018, 192: 67-74. DOI: 10.1016/j.saa.2017.10.044.
[16] ZHANG X, LIU C Y, CAI X Y, et al. A highly specific Golgi-targetable fluorescent probe for tracking cysteine generation during the Golgi stress response[J]. Sens Actuat B Chem, 2020, 310: 127820. DOI: 10.1016/j.snb.2020.127820.
[17] LENG S, QIAO Q L, MIAO L, et al. A wash-free SNAP-tag fluorogenic probe based on the additive effects of quencher release and environmental sensitivity[J]. Chem Commun, 2017, 53(48): 6448-6451. DOI: 10.1039/c7cc01483j.
[18] OHYANAGI T, SHIMA T, OKADA Y, et al. Compact and stable SNAP ligand-conjugated quantum dots as a fluorescent probe for single-molecule imaging of dynein motor protein[J]. Chem Commun, 2015, 51(80): 14836-14839. DOI: 10.1039/c5cc05526a. (
Outlines

/

〈 〉