Faye Audrey, Borthwick Karen, Esnous Catherine, Price Nigel T, Gobin Stéphanie, Jackson Vicky N, Zammit Victor A, Girard Jean, Prip-Buus Carina
Département d'Endocrinologie, Institut Cochin, INSERM U567, CNRS Unité Mixte de Recherche 8104, Université René Descartes, 24 rue du Faubourg Saint-Jacques, 75014 Paris, France.
Biochem J. 2005 Apr 1;387(Pt 1):67-76. doi: 10.1042/BJ20041533.
We have previously proposed that changes in malonyl-CoA sensitivity of rat L-CPT1 (liver carnitine palmitoyltransferase 1) might occur through modulation of interactions between its cytosolic N- and C-terminal domains. By using a cross-linking strategy based on the trypsin-resistant folded state of L-CPT1, we have now shown the existence of such N-C (N- and C-terminal domain) intramolecular interactions both in wild-type L-CPT1 expressed in Saccharomyces cerevisiae and in the native L-CPT1 in fed rat liver mitochondria. These N-C intramolecular interactions were found to be either totally (48-h starvation) or partially abolished (streptozotocin-induced diabetes) in mitochondria isolated from animals in which the enzyme displays decreased malonyl-CoA sensitivity. Moreover, increasing the outer membrane fluidity of fed rat liver mitochondria with benzyl alcohol in vitro, which induced malonyl-CoA desensitization, attenuated the N-C interactions. This indicates that the changes in malonyl-CoA sensitivity of L-CPT1 observed in mitochondria from starved and diabetic rats, previously shown to be associated with altered membrane composition in vivo, are partly due to the disruption of N-C interactions. Finally, we show that mutations in the regulatory regions of the N-terminal domain affect the ability of the N terminus to interact physically with the C-terminal domain, irrespective of whether they increased [S24A (Ser24-->Ala)/Q30A] or abrogated (E3A) malonyl-CoA sensitivity. Moreover, we have identified the region immediately N-terminal to transmembrane domain 1 (residues 40-47) as being involved in the chemical N-C cross-linking. These observations provide the first demonstration by a physico-chemical method that L-CPT1 adopts different conformational states that differ in their degree of proximity between the cytosolic N-terminal and the C-terminal domains, and that this determines its degree of malonyl-CoA sensitivity depending on the physiological state.
我们之前曾提出,大鼠肝脏肉碱棕榈酰转移酶1(L-CPT1)对丙二酰辅酶A敏感性的变化可能是通过调节其胞质N端和C端结构域之间的相互作用而发生的。通过基于L-CPT1抗胰蛋白酶折叠状态的交联策略,我们现已证明,在酿酒酵母中表达的野生型L-CPT1以及喂食大鼠肝脏线粒体中的天然L-CPT1中均存在这种N-C(N端和C端结构域)分子内相互作用。在从酶对丙二酰辅酶A敏感性降低的动物分离的线粒体中,发现这些N-C分子内相互作用要么完全消失(饥饿48小时),要么部分消失(链脲佐菌素诱导的糖尿病)。此外,在体外使用苯甲醇增加喂食大鼠肝脏线粒体的外膜流动性,这会诱导丙二酰辅酶A脱敏,减弱了N-C相互作用。这表明,在饥饿和糖尿病大鼠线粒体中观察到的L-CPT1对丙二酰辅酶A敏感性的变化(之前已证明与体内膜组成改变有关)部分是由于N-C相互作用的破坏。最后,我们表明,N端结构域调节区域的突变会影响N端与C端结构域物理相互作用的能力,无论它们是增加了(S24A(Ser24→Ala)/Q30A)还是消除了(E3A)丙二酰辅酶A敏感性。此外,我们已确定跨膜结构域1紧邻的N端区域(第40-47位残基)参与化学N-C交联。这些观察结果首次通过物理化学方法证明,L-CPT1采用不同的构象状态,其胞质N端和C端结构域之间的接近程度不同,并且这取决于生理状态决定其对丙二酰辅酶A的敏感程度。