Wu Chun-Hui, Ye Hong-De, Wu De-Hong, Yan Hong, Wang Xue-Mei, Chen Jun
State Key Lab of Bioelectronics (Chien-Shiung Wu Lab), Southeast University, Nanjing 210096, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2013 Jan;33(1):120-5.
The biointeractions between a series of new organometallic carborane derivatives and model protein bovine serum albumin (BSA) were investigated by means of fluorescence and synchronous spectroscopy. The observations demonstrate that the ferrocene-carborane conjugates (FcSB1, FcSB2 and FcSBCO) and the ruthenium(II)-arene carborane complexes (RuBFc and RuBCOOH) can form a steady complex with BSA and statically quench its fluorescence. The ferrocene-carborane conjugates could remarkably affect the tertiary structure of BSA and induce the microenvironment changes of Trp and Tyr residues from hydrophilic to hydrophobic environment. But the effect of the ruthenium(II)-arene carborane complexes on the tertiary structure of BSA is much less. This study would give meaningful insights into the evaluation of the promising biomedical applications of the new carborane derivatives and benefit the development of potential multifunctional metallodrugs.
通过荧光光谱和同步荧光光谱法研究了一系列新型有机金属碳硼烷衍生物与模型蛋白牛血清白蛋白(BSA)之间的生物相互作用。观察结果表明,二茂铁-碳硼烷共轭物(FcSB1、FcSB2和FcSBCO)以及钌(II)-芳烃碳硼烷配合物(RuBFc和RuBCOOH)能够与BSA形成稳定的复合物,并静态猝灭其荧光。二茂铁-碳硼烷共轭物能够显著影响BSA的三级结构,并诱导色氨酸(Trp)和酪氨酸(Tyr)残基的微环境从亲水性变为疏水性环境。但是钌(II)-芳烃碳硼烷配合物对BSA三级结构的影响要小得多。该研究将为评估新型碳硼烷衍生物在生物医学领域的潜在应用提供有意义的见解,并有助于开发潜在的多功能金属药物。