Mitochondrial carrier

Mitochondrial carrier family
Identifiers
Symbol	SLC25
TCDB	2.A.29

The Mitochondrial carrier family (MCF), also known as the solute carrier family 25 (SLC25), consists of a group of proteins that function in the transport of metabolites across the inner membranes of mitochondria. These carriers are crucial for the metabolic functions of mitochondria, including ATP synthesis, metabolism regulation, and maintenance of ion gradients.

Function

Mitochondrial carriers are integral membrane proteins that facilitate the exchange of substrates and products between the cytosol and the mitochondrial matrix. Each carrier typically transports a specific set of metabolites, which may include nucleotides, amino acids, coenzymes, and inorganic ions. The transport process is generally governed by the electrochemical gradient across the mitochondrial membrane.

Structure

The typical structure of a mitochondrial carrier consists of six transmembrane alpha-helices, with both the N-terminus and C-terminus located in the cytoplasm. These proteins often function as homodimers or homotrimers. The carriers possess signature motifs that are critical for their function, often referred to as the mitochondrial carrier signature.

Types of Mitochondrial Carriers

There are several types of mitochondrial carriers, each specialized for different functions:

• ADP/ATP carrier (AAC) - Transports ADP into and ATP out of the mitochondria, crucial for cellular energy management.
• Phosphate carrier (PiC) - Transports inorganic phosphate into the mitochondria, essential for ATP synthesis.
• Uncoupling proteins (UCPs) - Involved in creating permeability to protons, thus uncoupling ATP synthesis from electron transport.
• Dicarboxylate carrier - Transports dicarboxylates, such as malate and succinate, which are important for the citric acid cycle.
• Ketone body carriers - Transport ketone bodies, which are vital during fasting or diet-induced ketosis.

Genetic and Health Implications

Mutations in genes encoding mitochondrial carriers can lead to various metabolic disorders. For example, defects in the ADP/ATP carrier can result in mitochondrial myopathy and cardiomyopathy. Understanding the function and regulation of these carriers is crucial for developing therapeutic strategies against these metabolic diseases.

Research

Research in the field of mitochondrial carriers often focuses on understanding the detailed mechanisms of substrate specificity and regulation. Advances in structural biology, including X-ray crystallography and cryo-electron microscopy, have provided significant insights into the carrier structures.

See also

• Mitochondrion
• Cell metabolism
• Membrane transport protein