TRIM21 is an IgG receptor that is structurally, thermodynamically, and kinetically conserved

Proc Natl Acad Sci U S A. 2008 Apr 22;105(16):6045-50. doi: 10.1073/pnas.0800159105. Epub 2008 Apr 17.

Abstract

The newly identified tripartite motif (TRIM) family of proteins mediate innate immunity and other critical cellular functions. Here we show that TRIM21, which mediates the autoimmune diseases rheumatoid arthritis, systemic lupus erythematosus, and Sjögren's syndrome, is a previously undescribed IgG receptor with a binding mechanism unlike known mammalian Fcgamma receptors. TRIM21 simultaneously targets conserved hot-spot residues on both Ig domains of the Fc fragment using a PRYSPRY domain with a preformed multisite interface. The binding sites on both TRIM21 and Fc are highly conserved to the extent that the proteins are functionally interchangeable through murine, canine, primate, and human species. Pre-steady-state analysis exposes mechanistic conservation at the level of individual residues, which make the same energetic and kinetic contributions to binding despite varying in sequence. Together, our results reveal that TRIM21 is a previously undescribed type of IgG receptor based on a non-Ig scaffold whose interaction at the fundamental level-structural, thermodynamic, and kinetic-is evolutionarily conserved.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • DNA-Binding Proteins / chemistry*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology
  • Humans
  • Immunoglobulin G / immunology
  • Kinetics
  • Mice
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Nuclear Proteins / chemistry*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / immunology
  • Protein Structure, Tertiary
  • Receptors, IgG / chemistry*
  • Receptors, IgG / genetics
  • Receptors, IgG / immunology
  • Ribonucleoproteins / chemistry*
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / immunology
  • Sequence Alignment
  • Thermodynamics

Substances

  • DNA-Binding Proteins
  • Immunoglobulin G
  • Nuclear Proteins
  • Receptors, IgG
  • Ribonucleoproteins
  • SS-A antigen

Associated data

  • PDB/2VOK
  • PDB/2VOL