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首页> 外文期刊>FEBS Letters >Subunit exchange of lens α‐crystallin: a fluorescence energy transfer study with the fluorescent labeled αA‐crystallin mutant W9F as a probe
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Subunit exchange of lens α‐crystallin: a fluorescence energy transfer study with the fluorescent labeled αA‐crystallin mutant W9F as a probe

机译:晶状体α-晶状体蛋白的亚基交换:以荧光标记的αA-晶状体突变体W9F为探针的荧光能量转移研究

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>A Trp-free αA-crystallin mutant (W9F) was prepared by site-directed mutation. This mutant appears to be identical to the wild-type in terms of conformation (secondary and tertiary structures). W9F was labeled with a sulfhydryl-specific fluorescent probe, 2-(4′-maleimidylanilino) naphthalene-6-sulfonate (MIANS), and used in a subunit exchange between αA- and αA-crystallins as well as between αA- and αB-crystallins, studied by measurement of fluorescence resonance energy transfer. Energy transfer was observed between Trp (donor, with emission maximum at 336 nm) of wild-type αA- or αB-crystallin and MIANS (acceptor, with absorption maximum at 313 nm) of labeled W9F when subunit exchange occurred. Time-dependent decrease of Trp and increase of MIANS fluorescence were recorded. The exchange was faster at 37°C than at 25°C. The energy transfer efficiency was greater between homogeneous subunits (αA-αA) than between heterogeneous subunits (αA-αB). A previous exchange study with isoelectric focusing indicated a complete but slow exchange between αA and αB subunits. The present study showed that the exchange was a fast process, and the different energy transfer efficiencies between αA-αA and αA-αB indicated that αA- and αB-crystallins were not necessarily structurally equivalent.
机译:通过定点突变制备无Trp的αA-晶状蛋白突变体(W9F)。就构象(二级和三级结构)而言,该突变体似乎与野生型相同。 W9F用巯基特异性荧光探针2-(4'-maleimidylanilino)萘-6-磺酸盐(MIANS)标记,并用于αA-和αA-结晶蛋白之间以及αA-和αB-之间的亚基交换。结晶蛋白,通过测量荧光共振能量转移进行研究。当发生亚基交换时,在野生型αA-或αB-晶状蛋白的Trp(供体,最大发射在336 nm)与标记的W9F的MIANS(受体,最大吸收在313 nm)之间观察到能量转移。记录了时间依赖性的Trp减少和MIANS荧光增加。在37°C下的交换比在25°C下的交换更快。均质亚基(αA-αA)之间的能量转移效率高于异质亚基(αA-αB)之间的能量转移效率。以前的等电聚焦交换研究表明,αA和αB亚基之间完全但缓慢地交换。本研究表明,交换是一个快速的过程,并且αA-αA和αA-αB之间的能量转移效率不同,表明αA-和αB-晶状蛋白不一定在结构上相等。

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