The Druggability of Solute Carriers

J Med Chem. 2020 Apr 23;63(8):3834-3867. doi: 10.1021/acs.jmedchem.9b01237. Epub 2019 Dec 19.

Abstract

The transport of materials across membranes is a vital process for all aspects of cellular function, including growth, metabolism, and communication. Protein transporters are the molecular gates that control this movement and serve as key points of regulation for these processes, thus representing an attractive class of therapeutic targets. With more than 400 members, the solute carrier (SLC) membrane transport proteins are the largest family of transporters, yet, they are pharmacologically underexploited relative to other protein families and many of the available chemical tools possess suboptimal selectivity and efficacy. Fortuitously, there is increased interest in elucidating the physiological roles of SLCs as well as growing recognition of their therapeutic potential. This Perspective provides an overview of the SLC superfamily, including their biochemical and functional features, as well as their roles in various human diseases. In particular, we explore efforts and associated challenges toward drugging SLCs, as well as highlight opportunities for future drug discovery.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biological Transport / drug effects
  • Biological Transport / physiology
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism*
  • Drug Discovery / methods
  • Drug Discovery / trends*
  • Humans
  • Metabolic Diseases / drug therapy
  • Metabolic Diseases / metabolism
  • Nervous System Diseases / drug therapy
  • Nervous System Diseases / metabolism
  • Protein Structure, Secondary
  • Protein Transport / drug effects
  • Protein Transport / physiology
  • Sodium-Glucose Transporter 2 Inhibitors / administration & dosage
  • Sodium-Glucose Transporter 2 Inhibitors / chemistry
  • Solute Carrier Proteins / antagonists & inhibitors
  • Solute Carrier Proteins / chemistry*
  • Solute Carrier Proteins / metabolism*

Substances

  • Sodium-Glucose Transporter 2 Inhibitors
  • Solute Carrier Proteins