Unravelling the modus-operandi of chromenylium-cyanine fluorescent probes: a case study
文献信息
Ricardo Flores-Cruz, Rafael López-Arteaga, Lizbeth Ramírez-Vidal, Fernando López-Casillas, Arturo Jiménez-Sánchez
Small-molecule fluorescent probes having optimized optical properties, such as high photostability and brightness, local microenvironment sensitivity and specific subcellular localizations, are increasingly available. Although the basis for designing efficient fluorophores for bioimaging applications is well established, implementing an improvement in a given photophysical characteristic always tends to compromise another optical property. This problem has enormous consequences for in vivo imaging, where ensuring a specific localization and precise control of the probe response is challenging. Herein we discuss a fluorescent probe, CC334, as a case study of the chromenylium-cyanine family that commonly exhibits highly complex photophysical schemes and highly interfered bioanalytical responses. By an exhaustive and concise analysis of the CC334 optical responses including detailed spectroscopic calibrations, steady-state microenvironment effects, ultrafast photophysics analysis and computational studies, we elucidate a new strategy to apply the probe in the singlet oxygen reactive oxygen species (1O2-ROS) monitoring using in vitro and in vivo models. The probe provides a new avenue for designing fluorescent probes to understand the dynamic behavior of subcellular environments.
期刊推荐

Journal of Organometallic Chemistry

Science Progress

Proceedings of the National Academy of Sciences of the United States of America

Israel Journal of Chemistry

Planta Medica

Journal of Heterocyclic Chemistry

Organic Preparations and Procedures International

Nature

Kinetics and Catalysis

Journal of Physics and Chemistry of Solids
相关文献
Inserting an “atomic trap” for directional dopant migration in core/multi-shell quantum dots
Chun Chu, Elan Hofman, Chengpeng Gao, Shuya Li, Hanjie Lin, Walker MacSwain, John M. Franck, Robert W. Meulenberg, Arindam Chakraborty, Weiwei Zheng
DOI: 10.1039/D3SC04165D
Photocatalytic, modular difunctionalization of alkenes enabled by ligand-to-metal charge transfer and radical ligand transfer
Kang-Jie Bian, David Nemoto, Jr, Xiao-Wei Chen, Shih-Chieh Kao, James Hooson, Julian G. West
DOI: 10.1039/D3SC05231A
O–H bond activation of β,γ-unsaturated oximes via hydrogen atom transfer (HAT) and photoredox dual catalysis
Chen Zhu, Xiangyu Chen, Huifeng Yue, Tengfei Ji, Yiqiao Ma, Yuanyuan Cao, Rajesh Kancherla, Magnus Rueping
DOI: 10.1039/D3SC04410F
Highly dispersed Pd-based pseudo-single atoms in zeolites for hydrogen generation and pollutant disposal
Kai Zhang, Ning Wang, Yali Meng, Tianjun Zhang, Pu Zhao, Jihong Yu
DOI: 10.1039/D3SC05851D
Direct conversion of carboxylic acids to free thiols via radical relay acridine photocatalysis enabled by N–O bond cleavage
Dmitry L. Lipilin, Mikhail O. Zubkov, Mikhail D. Kosobokov, Alexander D. Dilman
DOI: 10.1039/D3SC05513B
An erythrocyte membrane-camouflaged fluorescent covalent organic framework for starving/nitric oxide/immunotherapy of triple-negative breast cancer
Fang Yuan, Cuiling Zhang, Xianzhu Luo, Shasha Cheng, Yingxin Zhu, Yuezhong Xian
DOI: 10.1039/D3SC02022C
Thermally activated delayed fluorescence in a deep red dinuclear iridium(iii) complex: a hidden mechanism for short luminescence lifetimes
Andrey V. Zaytsev, Amit Sil, Glib V. Baryshnikov, J. A. Gareth Williams, Fernando B. Dias, Valery N. Kozhevnikov
DOI: 10.1039/D3SC04450E
Selective chiral dimerization and folding driven by arene–perfluoroarene force
Qiuhong Cheng, Aiyou Hao, Pengyao Xing
DOI: 10.1039/D3SC05212E
Visible light-induced palladium–carbon bond weakening in catalytically relevant T-shaped complexes
Peter M. Waddell, Lei Tian, Anthony R. Scavuzzo, Lalu Venigalla, Gregory D. Scholes, Brad P. Carrow
DOI: 10.1039/D3SC02588H
您可能还喜欢
5-氯咪唑并[1,2-c]嘧啶(CAS号:1208086-02-5)适用哪些法规指南?
5-氯咪唑并[1,2-c]嘧啶需遵循多项法规指南,包括但不限于GHS(全球化学品统一分类和标签制度),用于危险品的分类和标签。此外,根据其用途,还需遵循REAC...
3-磺丙基十六烷基二甲基铵(CAS号:2281-11-0)应用于哪些行业?
3-磺丙基十六烷基二甲基铵广泛应用于医药、聚合物、传感器和半导体等领域。在医药行业,它作为乳化剂和稳定剂用于制备药物制剂;在聚合物行业中,作为增塑剂和抗静电剂;...
(R)-1-苄氧羰基-2-苄基哌嗪盐酸(CAS号:1217753-37-1)应用于哪些行业?
(R)-1-苄氧羰基-2-苄基哌嗪盐酸主要应用于医药、有机合成等行业。它作为药物合成中的中间体,具有重要的应用价值。此外,该化合物还可用于聚合物合成、传感器制造...
什么是Benzo[c][1,2,5]thiadiazole-5,6-dithiol(CAS号:127498-45-7)?
Benzo[c][1,2,5]thiadiazole-5,6-二硫醇是一种含硫的有机化合物,具有独特的化学结构。该化合物的分子式为C8H5NOS4,分子量为22...
处理(5-氯-2-甲基吲哚-3)-乙酸(CAS号:19017-52-8)时应注意哪些实验室安全事项?
处理(5-氯-2-甲基吲哚-3)-乙酸时应佩戴防护眼镜和手套,保护皮肤和眼睛。通风橱应开启以确保良好的通风。如果不慎接触皮肤或眼睛,应立即用大量清水冲洗并寻求医...
在合成中是否有生物素亚砜(CAS号:3376-83-8)的替代品?
在合成中,生物素亚砜的替代品包括生物素、生物素硫代半缩醛等。生物素硫代半缩醛作为生物素的衍生物,具有相似的化学性质,但在某些反应中可能表现出不同的行为。选择替代...
在合成中是否有(4-氟四氢-2H-吡喃-4-基)甲醇(CAS号:883442-46-4)的替代品?
在合成过程中,可以考虑使用含有类似结构的化合物作为替代品,例如4-氟-2-羟基-1,3-二氧戊环或其他含有相应氟原子的四氢呋喃衍生物。这些化合物在化学性质上与目...
2,3-二氢吡咯并[1,2-C]嘧啶-1,4-二酮(CAS号:223432-94-8)安全吗?
2,3-二氢吡咯并[1,2-C]嘧啶-1,4-二酮在处理时需要适当的安全措施。它属于一般化学品,虽然相对稳定,但在高温或强酸强碱条件下可能分解或发生化学反应。建...
如何储存反式-3-庚烯(CAS号:14686-14-7)?
反式-3-庚烯应储存在阴凉、通风良好的地方,避免阳光直射和高温。储存容器应密封,放置在温度不超过25℃的环境中,并远离火源和热源。建议使用耐腐蚀的容器,并确保良...
1-乙酰基-1H-吲哚-6-甲腈(CAS号:1017791-09-1)安全吗?
1-乙酰基-1H-吲哚-6-甲腈的毒性较低,但在操作时仍需谨慎。使用时应避免吸入其粉尘或烟雾,避免皮肤接触,佩戴防护眼镜和手套。
来源期刊
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.




