Sawada K, Hummel B C, Walfish P G
Biochem J. 1986 Sep 15;238(3):787-91. doi: 10.1042/bj2380787.
The role in the activation of microsomal 5'-deiodinase (5'-DI) of rat hepatic cytosolic components of Mr approx. 13,000 (Fraction B) was studied in the presence of various concentrations of thiol compounds such as dithiothreitol (DTT), dihydrolipoamide (DHLA), GSH, and 2-mercaptoethanol (2-ME). Although Fraction B (which was prepared by gel filtration to exclude GSH and GSSG) had no intrinsic 5'-DI activity, could not stimulate microsomal 5'-DI activity in the absence of added thiol and did not contain GSH as a mixed disulphide, it could produce a 3-fold increase in the maximal deiodinase activity achievable with DTT as well as other thiols, with the order being the same as the activation potency of these thiols in the absence of Fraction B (i.e. DHLA greater than DTT greater than 2-ME greater than GSH). These observations suggest that: a component of cytosolic Fraction B, designated 'deiodination factor B' (DFB), operates as an efficient intermediary to enhance activation of microsomal 5'-DI by thiols through a mechanism independent of GSH; thiols may participate in a non-specific thiol-disulphide exchange with inactive (oxidized) DFB to convert it into an active form that contains one or more thiol groups and is more effective than GSH or other thiols in facilitating the re-activation of inactive (oxidized) microsomal 5'-DI thiol (ESI) to its active state (ESH).
研究了在不同浓度的硫醇化合物(如二硫苏糖醇(DTT)、二氢硫辛酸(DHLA)、谷胱甘肽(GSH)和2-巯基乙醇(2-ME))存在下,大鼠肝脏胞质中约13,000 Mr的组分(组分B)在微粒体5'-脱碘酶(5'-DI)激活中的作用。尽管组分B(通过凝胶过滤制备以排除GSH和GSSG)没有内在的5'-DI活性,在未添加硫醇时不能刺激微粒体5'-DI活性,且不含有作为混合二硫化物的GSH,但它可以使DTT以及其他硫醇所能达到的最大脱碘酶活性提高3倍,其顺序与这些硫醇在没有组分B时的激活效力相同(即DHLA大于DTT大于2-ME大于GSH)。这些观察结果表明:胞质组分B中的一种成分,称为“脱碘因子B”(DFB),通过一种独立于GSH的机制,作为一种有效的中介物来增强硫醇对微粒体5'-DI的激活;硫醇可能与无活性(氧化的)DFB进行非特异性的硫醇-二硫化物交换,将其转化为一种含有一个或多个硫醇基团的活性形式,并且在促进无活性(氧化的)微粒体5'-DI硫醇(ESI)重新激活为其活性状态(ESH)方面比GSH或其他硫醇更有效。