Knudsen J, Jensen M V, Hansen J K, Faergeman N J, Neergaard T B, Gaigg B
Biokemisk Institut, Odense Universitet, Denmark.
Mol Cell Biochem. 1999 Feb;192(1-2):95-103. doi: 10.1007/978-1-4615-4929-1_11.
Long chain acylCoA esters (LCAs) act both as substrates and intermediates in intermediary metabolism and as regulators in various intracellular functions. AcylCoA binding protein (ACBP) binds LCAs with high affinity and is believed to play an important role in intracellular acylCoA transport and pool formation and therefore also for the function of LCAs as metabolites and regulators of cellular functions [1]. The major factors controlling the free concentration of cytosol long chain acylCoA ester (LCA) include ACBP [2], sterol carrier protein 2 (SCP2) [3] and fatty acid binding protein (FABP) [4]. Additional factors affecting the concentration of free LCA include feed back inhibition of the acylCoA synthetase [5], binding to acylCoA receptors (LCA-regulated molecules and enzymes), binding to membranes and the activity of acylCoA hydrolases [6].
长链脂酰辅酶A酯(LCAs)在中间代谢中既作为底物和中间体,又在各种细胞内功能中作为调节剂。酰基辅酶A结合蛋白(ACBP)以高亲和力结合LCAs,被认为在细胞内酰基辅酶A转运和库形成中起重要作用,因此对LCAs作为细胞功能的代谢物和调节剂的功能也很重要[1]。控制胞质长链脂酰辅酶A酯(LCA)游离浓度的主要因素包括ACBP[2]、固醇载体蛋白2(SCP2)[3]和脂肪酸结合蛋白(FABP)[4]。影响游离LCA浓度的其他因素包括酰基辅酶A合成酶的反馈抑制[5]、与酰基辅酶A受体(LCA调节的分子和酶)的结合、与膜的结合以及酰基辅酶A水解酶的活性[6]。