4.5 Review

Toll-like receptor signalling through macromolecular protein complexes

Journal

MOLECULAR IMMUNOLOGY
Volume 63, Issue 2, Pages 162-165

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.molimm.2014.06.033

Keywords

Toll-like receptor 4; Myddosome

Funding

  1. MRC
  2. Wellcome Trust [WT100321/z/12/Z, MRC G100133]
  3. Wellcome Trust [100321/Z/12/Z] Funding Source: Wellcome Trust
  4. BBSRC [BB/K006436/1] Funding Source: UKRI
  5. MRC [G1000133] Funding Source: UKRI
  6. Biotechnology and Biological Sciences Research Council [BB/K006436/1] Funding Source: researchfish
  7. Medical Research Council [G1000133] Funding Source: researchfish
  8. Wellcome Trust [100321/Z/12/Z] Funding Source: researchfish

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The molecular mechanisms by which pattern recognition receptors (PRRs) signal are increasingly well understood. Toll-like receptor 4 (TLR4) signals through two separate pairs of adaptor proteins Mal/MyD88 and Tram/Trif. Structural studies have revealed a common theme for PRR signalling in that their signalling proteins form large macromolecular complexes which are thought to form the active signalling complex. The first of these to be characterised was the MyD88 signalling complex Myddosome. Many questions remain unanswered however. In particular it is unclear whether these signalling complexes form within the living cell, how many of each signalling protein is within the intracellular Myddosome and whether the stoichiometry can vary in a ligand-dependent manner. In this review we will discuss what is known about the macromolecular complexes thought to be important for TLR4 signalling. (C) 2014 Elsevier Ltd. All rights reserved.

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