Lintao Wei , Junjie Wang , Jianhao Wu , Xidong Li , Qianying Zhou , Mengxu Sun , Bo Peng , Jun Chen , Bin Sun
{"title":"环金属化钌(II)复合物基纳米颗粒增强活细胞中microrna的检测和成像。","authors":"Lintao Wei , Junjie Wang , Jianhao Wu , Xidong Li , Qianying Zhou , Mengxu Sun , Bo Peng , Jun Chen , Bin Sun","doi":"10.1016/j.bios.2024.117090","DOIUrl":null,"url":null,"abstract":"<div><div>MicroRNA (miRNA) imaging in living cells is paramount for comprehending its dynamic functions and profiles, offering valuable insights into miRNA-related cellular processes. However, this remains challenging due to limited transfection agents and the low abundance of miRNAs. Herein, a smart nanosystem was proposed for miRNA imaging in living cells by ingeniously integrating cyclometalated ruthenium (II) nanoparticles (RuNPs) with a catalyzed hairpin assembly (CHA) strategy. Three cyclometalated ruthenium (II) complexes were synthesized and employed self-assembly technology to construct RuNPs. After evaluating their loading efficiency (L<sub>E</sub>), fluorescence quenching rates (Q<sub>E</sub>), and fluorescence recovery rates (R<sub>E</sub>) for Hairpins, RuNPs-1 was selected to construct the Hairpins@RuNPs-1 nanosystem. With a detection limit of 1.5 pM, the Hairpins@RuNPs-1 nanosystem demonstrated high sensitivity for miR-25, live cell imaging confirmed its ability to detect intracellular miR-25 and differentiate its expression in various cells with excellent biocompatibility. We believe it has the potential to become an effective tool for nucleic acid research and would be poised to significantly influence the diagnosis and treatment of diseases.</div></div>","PeriodicalId":259,"journal":{"name":"Biosensors and Bioelectronics","volume":"272 ","pages":"Article 117090"},"PeriodicalIF":10.7000,"publicationDate":"2024-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cyclometalated ruthenium (II) complex-based nanoparticles for enhanced microRNAs detection and imaging in living cells\",\"authors\":\"Lintao Wei , Junjie Wang , Jianhao Wu , Xidong Li , Qianying Zhou , Mengxu Sun , Bo Peng , Jun Chen , Bin Sun\",\"doi\":\"10.1016/j.bios.2024.117090\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>MicroRNA (miRNA) imaging in living cells is paramount for comprehending its dynamic functions and profiles, offering valuable insights into miRNA-related cellular processes. However, this remains challenging due to limited transfection agents and the low abundance of miRNAs. Herein, a smart nanosystem was proposed for miRNA imaging in living cells by ingeniously integrating cyclometalated ruthenium (II) nanoparticles (RuNPs) with a catalyzed hairpin assembly (CHA) strategy. Three cyclometalated ruthenium (II) complexes were synthesized and employed self-assembly technology to construct RuNPs. After evaluating their loading efficiency (L<sub>E</sub>), fluorescence quenching rates (Q<sub>E</sub>), and fluorescence recovery rates (R<sub>E</sub>) for Hairpins, RuNPs-1 was selected to construct the Hairpins@RuNPs-1 nanosystem. With a detection limit of 1.5 pM, the Hairpins@RuNPs-1 nanosystem demonstrated high sensitivity for miR-25, live cell imaging confirmed its ability to detect intracellular miR-25 and differentiate its expression in various cells with excellent biocompatibility. We believe it has the potential to become an effective tool for nucleic acid research and would be poised to significantly influence the diagnosis and treatment of diseases.</div></div>\",\"PeriodicalId\":259,\"journal\":{\"name\":\"Biosensors and Bioelectronics\",\"volume\":\"272 \",\"pages\":\"Article 117090\"},\"PeriodicalIF\":10.7000,\"publicationDate\":\"2024-12-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biosensors and Bioelectronics\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0956566324010972\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biosensors and Bioelectronics","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0956566324010972","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
Cyclometalated ruthenium (II) complex-based nanoparticles for enhanced microRNAs detection and imaging in living cells
MicroRNA (miRNA) imaging in living cells is paramount for comprehending its dynamic functions and profiles, offering valuable insights into miRNA-related cellular processes. However, this remains challenging due to limited transfection agents and the low abundance of miRNAs. Herein, a smart nanosystem was proposed for miRNA imaging in living cells by ingeniously integrating cyclometalated ruthenium (II) nanoparticles (RuNPs) with a catalyzed hairpin assembly (CHA) strategy. Three cyclometalated ruthenium (II) complexes were synthesized and employed self-assembly technology to construct RuNPs. After evaluating their loading efficiency (LE), fluorescence quenching rates (QE), and fluorescence recovery rates (RE) for Hairpins, RuNPs-1 was selected to construct the Hairpins@RuNPs-1 nanosystem. With a detection limit of 1.5 pM, the Hairpins@RuNPs-1 nanosystem demonstrated high sensitivity for miR-25, live cell imaging confirmed its ability to detect intracellular miR-25 and differentiate its expression in various cells with excellent biocompatibility. We believe it has the potential to become an effective tool for nucleic acid research and would be poised to significantly influence the diagnosis and treatment of diseases.
期刊介绍:
Biosensors & Bioelectronics, along with its open access companion journal Biosensors & Bioelectronics: X, is the leading international publication in the field of biosensors and bioelectronics. It covers research, design, development, and application of biosensors, which are analytical devices incorporating biological materials with physicochemical transducers. These devices, including sensors, DNA chips, electronic noses, and lab-on-a-chip, produce digital signals proportional to specific analytes. Examples include immunosensors and enzyme-based biosensors, applied in various fields such as medicine, environmental monitoring, and food industry. The journal also focuses on molecular and supramolecular structures for enhancing device performance.