Acyl‐CoA binding proteins: Multiplicity and function

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Abstract
The physiological role of long‐chain fatty acyl‐CoA is thought to be primarily in intermediary metabolism of fatty acids. However, recent data show that nM to μM levels of these lipophilic molecules are potent regulators of cell functionsin vitro. Although long‐chain fatty acyl‐CoA are present at several hundred μM concentration in the cell, very little long‐chain fatty acyl‐CoA actually exists as free or unbound molecules, but rather is bound with high affinity to membrane lipids and/or proteins. Recently, there is growing awareness that cytosol contains nonenzymatic proteins also capable of binding long‐chain fatty acyl‐CoA with high affinity. Although the identity of the cytosolic long‐chain fatty acyl‐CoA binding protein(s) has been the subject of some controversy, there is growing evidence that several diverse nonenzymatic cytosolic proteins will bind long‐chain fatty acyl‐CoA. Not only does acyl‐CoA binding protein specifically bind medium and long‐chain fatty acyl‐CoA (LCFA‐CoA), but ubiquitous proteins with multiple ligand specificities such as the fatty acid binding proteins and sterol carrier protein‐2 also bind LCFA‐CoA with high affinity. The potential of these acyl‐CoA binding proteins to influence the level of free LCFA‐CoA and thereby the amount of LCFA‐CoA bound to regulatory sites in proteins and enzymes is only now being examined in detail. The purpose of this article is to explore the identity, nature, function, and pathobiology of these fascinating newly discovered long‐chain fatty acyl‐CoA binding proteins. The relative contributions of these three different protein families to LCFA‐CoA utilization and/or regulation of cellular activities are the focus of new directions in this field.

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