The START-domain proteins in intracellular lipid transport and beyond

Mol Cell Endocrinol. 2020 Mar 15:504:110704. doi: 10.1016/j.mce.2020.110704. Epub 2020 Jan 10.

Abstract

The Steroidogenic Acute Regulatory Protein-related Lipid Transfer (START) domain is a ~210 amino acid sequence that folds into an α/β helix-grip structure forming a hydrophobic pocket for lipid binding. The helix-grip fold structure defines a large superfamily of proteins, and this review focuses on the mammalian START domain family members that include single START domain proteins with identified ligands, and larger multi-domain proteins that may have novel roles in metabolism. Much of our understanding of the mammalian START domain proteins in lipid transport and changes in metabolism has advanced through studies using knockout mouse models, although for some of these proteins the identity and/or physiological role of ligand binding remains unknown. The findings that helped define START domain lipid-binding specificity, lipid transport, and changes in metabolism are presented to highlight that fundamental questions remain regarding the biological function(s) for START domain-containing proteins.

Keywords: Lipid trafficking; Metabolism; START domain.

Publication types

  • Review

MeSH terms

  • Animals
  • Biological Transport / genetics
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Carrier Proteins / physiology*
  • Humans
  • Intracellular Space / metabolism
  • Lipid Metabolism* / genetics
  • Membrane Transport Proteins / chemistry
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • Membrane Transport Proteins / physiology*
  • Mice
  • Mice, Knockout
  • Phosphoproteins / chemistry
  • Phosphoproteins / genetics
  • Phosphoproteins / physiology*
  • Steroidogenic Acute Regulatory Protein

Substances

  • Carrier Proteins
  • Membrane Transport Proteins
  • Phosphoproteins
  • Steroidogenic Acute Regulatory Protein