Volker K W, Reinitz C A, Knull H R
Department of Biochemistry and Molecular Biology, School of Medicine, University of North Dakota, Grand Forks 58202, USA.
Comp Biochem Physiol B Biochem Mol Biol. 1995 Nov;112(3):503-14. doi: 10.1016/0305-0491(95)00096-8.
The ability of glycolytic enzymes, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), aldolase, pyruvate kinase (PK), and lactate dehydrogenase muscle-type (LDH(M)), to generate interactive microtubule networks was investigated. Bundles have previously been defined as the parallel alignment of several microtubules and are one form of microtubule networks. Utilizing transmission electron microscopy, interactive networks of microtubules as well as bundles were readily observed in the presence of GAPDH, aldolase, or PK. These networks appear morphologically as cross-linked microtubules, oriented in many different ways. Light scattering indicated that the muscle forms of GAPDH, aldolase, PK and LDH(m) caused formation of the microtubule networks. Triose phosphate isomerase (TPI) and lactate dehydrogenase heart-type (LDH(H)), glycolytic enzymes which do not interact with tubulin or microtubules, did not produce bundles, or interactive networks. Sedimentation experiments confirmed that the enzymes that cross-link also co-pellet with the microtubules. Such cross-linking of microtubules indicate that the enzymes are multivalent with the capability of simultaneous binding to more than one microtubule.
研究了糖酵解酶甘油醛-3-磷酸脱氢酶(GAPDH)、醛缩酶、丙酮酸激酶(PK)和肌肉型乳酸脱氢酶(LDH(M))生成相互作用微管网络的能力。束状结构此前被定义为几根微管的平行排列,是微管网络的一种形式。利用透射电子显微镜,在存在GAPDH、醛缩酶或PK的情况下,很容易观察到微管以及束状结构的相互作用网络。这些网络在形态上表现为交联的微管,以许多不同的方式排列。光散射表明,GAPDH、醛缩酶、PK和LDH(m)的肌肉形式导致了微管网络的形成。磷酸丙糖异构酶(TPI)和心脏型乳酸脱氢酶(LDH(H)),这两种不与微管蛋白或微管相互作用的糖酵解酶,不会产生束状结构或相互作用网络。沉降实验证实,能够交联的酶也会与微管一起共同沉淀。微管的这种交联表明这些酶是多价的,能够同时结合不止一根微管。