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溴酚蓝结合蛋白结构及稳定性的研究

Research on the Structures and Stability ofBromophenol Blue-Binding Protein
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摘要 在早期对溴酚蓝结合蛋白(BPBBP)的研究中,我们确定了其在电泳谱中的位置及分子量。目前进行的实验中,我们从不同患者血清中BPBBP的存在及正常人的血清中BPBBP的结构和稳定性等方面对BPBBP进行了测定。测定的结果:(1)在不同患者血清中都不同程度地存在着BPBBP,这为寻求基因药物载体提供了新思路。(2)不同pH下,紫外-可见光连续光谱的结果说明BPBBP与溴酚蓝发生了化学键的结合,并结合稳定;只有当BPBBP的二级结构被破坏时,方可同溴酚蓝解离;溴酚蓝结构中的发色团也参与了结合,同时BPBBP与溴酚蓝的结合需要电荷的存在;(3)荧光光谱和荧光淬灭及温度淬灭的结果:BPBBP中位于分子外部的Trp,Tys,Phe占Trp,Tys,Phe总量的60%,内部的占40%;在75℃时BPBBP发生热变性,说明BPBBP的热稳定性较好,这也是基因药物的应用基础之一。 We have detected the band and molecular weight of bromophenol bluebinding protein (BPBBP) in the early research.Recent studies in our laboratory revealed that: (1) There were always different levels of amount of BPBBP in different patients′ albumin; (2) At different pH, the result of ultrovoilet visible continuing spectra suggested that the BPBBP binding with bromophenolblue by chemicalbinding was stable and the BPBBP can apart from bromophenolblue only when the secondary structure of BPBBP was broken; and the colorablemass of bromophenolblue also took part in the binding, meanwhile the bpbbp can not bind with bromophenolblue without electricity; (3) From the result of fluorescence spectrum and fluorescence puenched experiments, we found that there were 60 per cent of Trp, Tys and phe outside the BPBBP and 40 per cent inside; and from the result of temperature puenched experiments we also find that BPBBP denatured at 75 ℃.This result told us that the thermal stability of the BPBBP is more stable and this is one of the bases of application of gene drugs as well.
出处 《解放军医学高等专科学校学报》 1998年第3期10-12,共3页 Clinical Journal of Medical Officer
关键词 溴酚蓝结合蛋白 紫外-可见光连续光谱 荧光光谱 BPBBP ultrovoilet-visible continuing spectrum fluorescence spectrum
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