Fraser F, Corstorphine C G, Zammit V A
Hannah Research Institute, Ayr KA6 5HL, Scotland, U.K.
Biochem J. 1997 May 1;323 ( Pt 3)(Pt 3):711-8. doi: 10.1042/bj3230711.
The topology of carnitine palmitoyltransferase I (CPT I) in the outer membrane of rat liver mitochondria was studied using several approaches. 1. The accessibility of the active site and malonyl-CoA-binding site of the enzyme from the cytosolic aspect of the membrane was investigated using preparations of octanoyl-CoA and malonyl-CoA immobilized on to agarose beads to render them impermeant through the outer membrane. Both immobilized ligands were fully able to interact effectively with CPT I. 2. The effects of proteinase K and trypsin on the activity and malonyl-CoA sensitivity of CPT I were studied using preparations of mitochondria that were either intact or had their outer membranes ruptured by hypo-osmotic swelling (OMRM). Proteinase K had a marked but similar effect on CPT I activity irrespective of whether only the cytosolic or both sides of the membrane were exposed to it. However, it affected sensitivity more rapidly in OMRM. By contrast, trypsin only reduced CPT I activity when incubated with OMRM. The sensitivity of the residual CPT I activity was unaffected by trypsin. 3. The proteolytic fragments generated by these treatments were studied by Western blotting using three anti-peptide antibodies raised against linear epitopes of CPT I. These showed that a proteinase K-sensitive site close to the N-terminus was accessible from the cytosolic side of the membrane. No trypsin-sensitive sites were accessible in intact mitochondria. In OMRM, both proteinase K and trypsin acted from the inter-membrane space side of the membrane. 4. The ability of intact mitochondria and OMRM to bind to each of the three anti-peptide antibodies was used to study the accessibility of the respective epitopes on the cytosolic and inter-membrane space sides of the membrane. 5. The results of all these approaches indicate that CPT I adopts a bitopic topology within the mitochondrial outer membrane; it has two transmembrane domains, and both the N- and C-termini are exposed on the cytosolic side of the membrane, whereas the linker region between the transmembrane domains protrudes into the intermembrane space.
采用多种方法研究了肉碱棕榈酰转移酶I(CPT I)在大鼠肝脏线粒体外膜中的拓扑结构。1. 使用固定在琼脂糖珠上的辛酰辅酶A和丙二酰辅酶A制剂,研究了该酶活性位点和丙二酰辅酶A结合位点从膜的胞质侧的可及性,以使它们不能透过外膜。两种固定化配体都完全能够与CPT I有效相互作用。2. 使用完整的线粒体制剂或通过低渗肿胀使其外膜破裂的线粒体制剂(OMRM),研究了蛋白酶K和胰蛋白酶对CPT I活性和丙二酰辅酶A敏感性的影响。蛋白酶K对CPT I活性有显著但相似的影响,无论仅膜的胞质侧还是两侧都暴露于其中。然而,它在OMRM中对敏感性的影响更快。相比之下,胰蛋白酶仅在与OMRM一起孵育时才降低CPT I活性。残余CPT I活性的敏感性不受胰蛋白酶影响。3. 使用针对CPT I线性表位产生的三种抗肽抗体,通过蛋白质印迹法研究了这些处理产生的蛋白水解片段。这些结果表明,靠近N端的一个蛋白酶K敏感位点可从膜的胞质侧接近。在完整的线粒体中没有可接近的胰蛋白酶敏感位点。在OMRM中,蛋白酶K和胰蛋白酶都从膜的膜间隙侧起作用。4. 利用完整线粒体和OMRM与三种抗肽抗体各自结合的能力,研究了膜的胞质侧和膜间隙侧相应表位的可及性。5. 所有这些方法的结果表明,CPT I在线粒体外膜内采用双拓扑结构;它有两个跨膜结构域,N端和C端都暴露在膜的胞质侧,而跨膜结构域之间的连接区伸入膜间隙。