Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, People's Republic of China.
Inorg Chem. 2009 Jul 6;48(13):6011-25. doi: 10.1021/ic900412n.
Three luminescent cyclometalated iridium(III) bis-biotin complexes Ir(N(wedge)C)(2)(N(wedge)N) (HN(wedge)C = 2-(4-(N-(6-(biotinamido)hexyl)aminomethyl)phenyl)pyridine, HppyC6B, N(wedge)N = 2,2'-bipyridine, bpy (1); HN(wedge)C = 2-phenylpyridine, Hppy, N(wedge)N = 4,4'-bis((2-(biotinamido)ethyl)aminocarbonyl)-2,2'-bipyridine, bpyC2B2 (2); HN(wedge)C = Hppy, N(wedge)N = 4,4'-bis((2-((6-(biotinamido)hexanoyl)amino)ethyl)aminocarbonyl)-2,2'-bipyridine, bpyC2C6B2 (3)) and one tris-biotin complex Ir(ppyC6B)(2)(bpyC6B) (bpyC6B = 4-((6-(biotinamido)hexyl)aminocarbonyl)-4'-methyl-2,2'-bipyridine) (4) have been synthesized and characterized. The biotin-free complex Ir(ppy)(2)(bpyC4) (bpyC4 = 4,4'-bis(n-butylaminocarbonyl)-2,2'-bipyridine) (5) has also been prepared for comparison studies. Upon photoexcitation, all the complexes displayed intense and long-lived greenish-yellow to red triplet metal-to-ligand charge-transfer ((3)MLCT) (dpi (Ir) --> pi*(N(wedge)N)) emission in fluid solutions at room temperature and in low-temperature glass. Cyclic voltammetric studies revealed iridium(IV/III) oxidation at about +1.21 to + 1.29 V and diimine-based reductions at about -1.07 to -1.39 V versus SCE. The interactions of the bis-biotin and tris-biotin complexes with avidin have been studied by 4'-hydroxyazobenzene-2-carboxylic acid (HABA) assays, emission titrations, and dissociation assays. The possibility of these complexes as cross-linkers for avidin has been examined by microscopy studies using avidin-conjugated green fluororescent microspheres and size-exclusion HPLC analysis. Utilization of these luminescent iridium(III) biotin complexes in signal amplification has been demonstrated using avidin-coated nonfluorescent microspheres and complex 3 as an example. Additionally, the lipophilicity of all the complexes has been determined by reversed-phase HPLC. The cytotoxicity of these iridium(III) complexes toward the human cervix epithelioid carcinoma (HeLa) cell line has been evaluated by 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyltetrazolium bromide (MTT) assays. Furthermore, the cellular uptake of the complexes has been examined by ICP-MS, laser-scanning confocal microscopy, and flow cytometry.
三种发光的环金属铱(III)双生物素配合物 Ir(N(wedge)C)(2)(N(wedge)N) (HN(wedge)C = 2-(4-(N-(6-(生物素酰胺基)己基)氨基甲基)苯基)吡啶,HppyC6B,N(wedge)N = 2,2'-联吡啶,bpy (1); HN(wedge)C = 2-苯基吡啶,Hppy,N(wedge)N = 4,4'-双((2-(生物素酰胺基)乙基)氨基羰基)-2,2'-联吡啶,bpyC2B2 (2); HN(wedge)C = Hppy,N(wedge)N = 4,4'-双((2-((6-(生物素酰胺基)己酰基)氨基)乙基)氨基羰基)-2,2'-联吡啶,bpyC2C6B2 (3)) 和一种三生物素配合物 Ir(ppyC6B)(2)(bpyC6B) (bpyC6B = 4-((6-(生物素酰胺基)己基)氨基羰基)-4'-甲基-2,2'-联吡啶) (4) 已被合成并表征。为了进行比较研究,还制备了无生物素的配合物 Ir(ppy)(2)(bpyC4) (bpyC4 = 4,4'-双(n-丁基氨基羰基)-2,2'-联吡啶) (5)。在室温下和低温玻璃中,所有配合物在流体溶液中均显示出强烈且长寿命的绿黄色到红色三重态金属到配体电荷转移((3)MLCT)(dpi(Ir)-> pi*(N(wedge)N)) 发射。循环伏安研究表明,铱(IV/III)氧化在约+1.21 到+1.29 V,二亚胺基还原在约-1.07 到-1.39 V 相对于 SCE。通过 4'-羟基偶氮苯甲酸-2-羧酸(HABA)测定、发射滴定和离解测定研究了双生物素和三生物素配合物与亲和素的相互作用。通过使用亲和素结合的绿色荧光微球和尺寸排阻 HPLC 分析,研究了这些配合物作为亲和素交联剂的可能性。利用这些发光的铱(III)生物素配合物在信号放大中的应用已通过使用亲和素包被的非荧光微球和配合物 3 进行了证明。此外,还通过反相 HPLC 测定了所有配合物的亲脂性。通过 3-(4,5-二甲基-2-噻唑基)-2,5-二苯基四氮唑溴盐(MTT)测定评估了这些铱(III)配合物对人宫颈上皮样癌细胞系(HeLa)的细胞毒性。此外,通过 ICP-MS、激光扫描共聚焦显微镜和流式细胞术研究了配合物的细胞摄取。