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Crystallization and preliminary X-ray diffraction analysis of the interleukin-3 alpha receptor bound to the Fab fragment of antibody CSL362

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INT UNION CRYSTALLOGRAPHY
DOI: 10.1107/S2053230X14002593

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  1. National Health and Medical Research Council of Australia (NHMRC)
  2. Cancer Australia
  3. Australian Cancer Research Foundation
  4. Victorian Government Operational Infrastructure Support Scheme
  5. Leukaemia Foundation

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Interleukin-3 (IL-3) is a member of the beta common family of cytokines that regulate multiple functions of myeloid cells. The IL-3 receptor-specific alpha subunit (IL3R alpha) is overexpressed on stem cells/progenitor cells of patients with acute myeloid leukaemia, where elevated receptor expression correlates clinically with a reduced patient survival rate. The monoclonal antibody (MAb) CSL362 is a humanized MAb derived from the murine MAb 7G3, originally identified for its ability to specifically recognize the human IL-3 receptor and for blocking the signalling of IL-3 in myeloid and endothelial cells. In order to elucidate the molecular mechanism of CSL362 antagonism, a preliminary structure of human IL3R alpha in complex with the MAb CSL362 has been determined.

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