Wagenknecht T, Francis N, DeRosier D J
J Mol Biol. 1983 Apr 15;165(3):523-39. doi: 10.1016/s0022-2836(83)80217-4.
The quaternary structure of the alpha-ketoglutarate dehydrogenase complex (KGDC) from Escherichia coli has been investigated by electron microscopy. KGDC consists of an octahedral cube-shaped structural core, lipoyl transsuccinylase (E2), to which 12 polypeptide chains each of alpha-ketoglutarate dehydrogenase (E1) and dihydrolipoyl dehydrogenase (E3) are non-covalently bound. The analysis was greatly simplified by analyzing subcomplexes of KGDC prepared by assembly of the purified component enzymes in vitro; the subcomplexes consisted of the E2 component to which only a few E1 or E3 subunits were attached. We find that both the E1 and E3 bind on the surface of the E2 molecule approximately midway between the 4-fold and 2-fold symmetry axes of E2. There are 24 such positions per E2 molecule but, based upon the observed stoichiometries of the component enzymes, it is clear that at least half of these sites are unoccupied in KGDC. If KGDC possesses symmetry, then a mechanism must exist for selecting a symmetrically distributed subset of the potential binding sites for the E1 and E3. However, analysis of images of subcomplexes in which two E1 or E3 subunits are present suggests that binding to the E2 occurs through random selection of the potential binding sites. If native KGDC is assembled by such a mechanism, then KGDC would not have a unique quaternary structure, but instead would consist of a family of structural isomers having up to approximately 125,000 members. Consideration of independent structural and biochemical data regarding the mechanism of action of the E2 indicates that the kind of structural heterogeneity being proposed is consistent with a functional KGDC.
通过电子显微镜对大肠杆菌α-酮戊二酸脱氢酶复合体(KGDC)的四级结构进行了研究。KGDC由一个八面体立方体形的结构核心——硫辛酰转琥珀酰酶(E2)组成,12条α-酮戊二酸脱氢酶(E1)和二氢硫辛酰脱氢酶(E3)的多肽链非共价结合于其上。通过分析体外组装纯化的组成酶制备的KGDC亚复合体,分析工作得以大大简化;这些亚复合体由仅连接有少数E1或E3亚基的E2组分组成。我们发现E1和E3都结合在E2分子表面,大约在E2的四重对称轴和二重对称轴之间的中间位置。每个E2分子有24个这样的位置,但根据观察到的组成酶的化学计量,很明显在KGDC中这些位点至少有一半未被占据。如果KGDC具有对称性,那么必然存在一种机制来选择E1和E3潜在结合位点的对称分布子集。然而,对存在两个E1或E3亚基的亚复合体图像的分析表明,与E2的结合是通过随机选择潜在结合位点发生的。如果天然KGDC是通过这样一种机制组装的,那么KGDC将不会有独特的四级结构,而是由多达约125,000个成员的结构异构体家族组成。对关于E2作用机制的独立结构和生化数据的考虑表明,所提出的这种结构异质性与功能性KGDC是一致的。