3EJJ : Structure of M-CSF bound to the first three domains of FMS

  • Xiaoyan Chen (Contributor)
  • Heli Liu (Contributor)
  • Pamela J Focia (Contributor)
  • Ann Hye Ryong Shim (Contributor)
  • Xiaolin He (Contributor)



Experimental Technique/Method:X-RAY DIFFRACTION
Release Date:2008-12-09
Deposition Date:2008-09-18
Revision Date:2011-07-13
Molecular Weight:69325.69
Macromolecule Type:Protein
Residue Count:599
Atom Site Count:4559

Macrophage colony stimulating factor (M-CSF), through binding to its receptor FMS, a class III receptor tyrosine kinase (RTK), regulates the development and function of mononuclear phagocytes, and plays important roles in innate immunity, cancer and inflammation. We report a 2.4 A crystal structure of M-CSF bound to the first 3 domains (D1-D3) of FMS. The ligand binding mode of FMS is surprisingly different from KIT, another class III RTK, in which the major ligand-binding domain of FMS, D2, uses the CD and EF loops, but not the beta-sheet on the opposite side of the Ig domain as in KIT, to bind ligand. Calorimetric data indicate that M-CSF cannot dimerize FMS without receptor-receptor interactions mediated by FMS domains D4 and D5. Consistently, the structure contains only 1 FMS-D1-D3 molecule bound to a M-CSF dimer, due to a weak, hydrophilic M-CSF:FMS interface, and probably a conformational change of the M-CSF dimer in which binding to the second site is rendered unfavorable by FMS binding at the first site. The partial, intermediate complex suggests that FMS may be activated in two steps, with the initial engagement step distinct from the subsequent dimerization/activation step. Hence, the formation of signaling class III RTK complexes can be diverse, engaging various modes of ligand recognition and various mechanistic steps for dimerizing and activating receptors.
Date made available2008

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