{"title":"一种带有双臂苯并咪唑配体的钌(II)配合物作为g -四联发光探针","authors":"Liang Ma, Xue-Wen Liu, Geng-Jun He, Xia Hu, Yuan-Dao Chen, Song-Bai Zhang","doi":"10.1002/aoc.7996","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>The selective detection of G-quadruplex DNA has the potential to reveal its biological function and provide important information for cancer diagnosis and treatment. Herein, a ruthenium(II) complex containing a two-armed benzimidazole ligand (bimbpy) (<b>RC1</b>) has been developed as a selective luminescence probe toward G4 DNA. <b>RC1</b> exhibited distinguishable luminescence response to G4 DNA, such as HTDNA, c-MYC, and 22AG. Especially, in the presence of HTDNA, the luminescence intensity of <b>RC1</b> increased to 6.1-fold. The limit of detection is 30 nM for HTDNA. However, it showed a small change in luminescence intensity against doubled-strand and single-strand DNA. The DNA binding experimental results indicated that <b>RC1</b> effectively stabilized G4 DNA through hydrogen bonds and π-π stacking. The selectivity of <b>RC1</b> to G4 DNA might be due to the increase in the rigidity of the two-armed benzimidazole ligand after binding to G4 DNA. Therefore, the design of ruthenium(II) complexes with a two-armed ligand will be an effective method to obtain Ru(II)-based G-quadruplex luminescent probes by adjusting the degree of rigidity of the two arms.</p>\n </div>","PeriodicalId":8344,"journal":{"name":"Applied Organometallic Chemistry","volume":"39 2","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Ruthenium(II) Complex With a Two-Armed Benzimidazole Ligand as the G-Quadruplex Luminescent Probe\",\"authors\":\"Liang Ma, Xue-Wen Liu, Geng-Jun He, Xia Hu, Yuan-Dao Chen, Song-Bai Zhang\",\"doi\":\"10.1002/aoc.7996\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>The selective detection of G-quadruplex DNA has the potential to reveal its biological function and provide important information for cancer diagnosis and treatment. Herein, a ruthenium(II) complex containing a two-armed benzimidazole ligand (bimbpy) (<b>RC1</b>) has been developed as a selective luminescence probe toward G4 DNA. <b>RC1</b> exhibited distinguishable luminescence response to G4 DNA, such as HTDNA, c-MYC, and 22AG. Especially, in the presence of HTDNA, the luminescence intensity of <b>RC1</b> increased to 6.1-fold. The limit of detection is 30 nM for HTDNA. However, it showed a small change in luminescence intensity against doubled-strand and single-strand DNA. The DNA binding experimental results indicated that <b>RC1</b> effectively stabilized G4 DNA through hydrogen bonds and π-π stacking. The selectivity of <b>RC1</b> to G4 DNA might be due to the increase in the rigidity of the two-armed benzimidazole ligand after binding to G4 DNA. Therefore, the design of ruthenium(II) complexes with a two-armed ligand will be an effective method to obtain Ru(II)-based G-quadruplex luminescent probes by adjusting the degree of rigidity of the two arms.</p>\\n </div>\",\"PeriodicalId\":8344,\"journal\":{\"name\":\"Applied Organometallic Chemistry\",\"volume\":\"39 2\",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-01-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Organometallic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/aoc.7996\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Organometallic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/aoc.7996","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
摘要
g -四重体DNA的选择性检测有可能揭示其生物学功能,并为癌症的诊断和治疗提供重要信息。在这里,钌(II)配合物含有双臂苯并咪唑配体(bimbpy) (RC1)已被开发作为G4 DNA的选择性发光探针。RC1对HTDNA、c-MYC和22AG等G4 DNA有明显的发光响应。特别是在HTDNA的存在下,RC1的发光强度增加到6.1倍。HTDNA的检出限为30 nM。然而,它对双链和单链DNA的发光强度变化很小。DNA结合实验结果表明,RC1通过氢键和π-π堆叠有效地稳定了G4 DNA。RC1对G4 DNA的选择性可能是由于双臂苯并咪唑配体与G4 DNA结合后刚性增加所致。因此,设计带有双臂配体的钌(II)配合物将是一种有效的方法,通过调整双臂的刚性程度来获得Ru(II)基g -四联发光探针。
A Ruthenium(II) Complex With a Two-Armed Benzimidazole Ligand as the G-Quadruplex Luminescent Probe
The selective detection of G-quadruplex DNA has the potential to reveal its biological function and provide important information for cancer diagnosis and treatment. Herein, a ruthenium(II) complex containing a two-armed benzimidazole ligand (bimbpy) (RC1) has been developed as a selective luminescence probe toward G4 DNA. RC1 exhibited distinguishable luminescence response to G4 DNA, such as HTDNA, c-MYC, and 22AG. Especially, in the presence of HTDNA, the luminescence intensity of RC1 increased to 6.1-fold. The limit of detection is 30 nM for HTDNA. However, it showed a small change in luminescence intensity against doubled-strand and single-strand DNA. The DNA binding experimental results indicated that RC1 effectively stabilized G4 DNA through hydrogen bonds and π-π stacking. The selectivity of RC1 to G4 DNA might be due to the increase in the rigidity of the two-armed benzimidazole ligand after binding to G4 DNA. Therefore, the design of ruthenium(II) complexes with a two-armed ligand will be an effective method to obtain Ru(II)-based G-quadruplex luminescent probes by adjusting the degree of rigidity of the two arms.
期刊介绍:
All new compounds should be satisfactorily identified and proof of their structure given according to generally accepted standards. Structural reports, such as papers exclusively dealing with synthesis and characterization, analytical techniques, or X-ray diffraction studies of metal-organic or organometallic compounds will not be considered. The editors reserve the right to refuse without peer review any manuscript that does not comply with the aims and scope of the journal. Applied Organometallic Chemistry publishes Full Papers, Reviews, Mini Reviews and Communications of scientific research in all areas of organometallic and metal-organic chemistry involving main group metals, transition metals, lanthanides and actinides. All contributions should contain an explicit application of novel compounds, for instance in materials science, nano science, catalysis, chemical vapour deposition, metal-mediated organic synthesis, polymers, bio-organometallics, metallo-therapy, metallo-diagnostics and medicine. Reviews of books covering aspects of the fields of focus are also published.