Maret Wolfgang
Departments of Preventive Medicine & Community Health and Anesthesiology, The University of Texas Medical Branch, Galveston, TX 77555-1109, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Oct 15;877(28):3378-83. doi: 10.1016/j.jchromb.2009.06.014. Epub 2009 Jun 13.
Fluorescence methods have been instrumental in demonstrating that the structure of human metallothionein in vivo depends on the availability of metal ions and the redox environment. Differential chemical modifications of its cysteine thiols with fluorescent probes allowed determination of three states: metallothionein (zinc-bound thiolate), thionein (free thiols), and thionin (disulfides). Interrogation of its zinc-binding properties with fluorescent chelating agents revealed that the affinities for the seven zinc ions vary over four orders of magnitude. Attachment of fluorescent labels generated metallothionein FRET (fluorescence resonance energy transfer) sensors for investigating its structure and function in living cells.
荧光方法在证明体内人类金属硫蛋白的结构取决于金属离子的可用性和氧化还原环境方面发挥了重要作用。用荧光探针进行的半胱氨酸硫醇的差异化学修饰可以确定三种状态:金属硫蛋白(锌结合硫醇盐)、硫蛋白(游离硫醇)和硫宁(二硫键)。用荧光螯合剂研究其锌结合特性表明,对七个锌离子的亲和力在四个数量级上变化。荧光标记的附着产生了用于研究其在活细胞中的结构和功能的金属硫蛋白荧光共振能量转移(FRET)传感器。