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A Fully Human Inhibitory Monoclonal Antibody to the Wnt Receptor RYK
Author(s) -
Michael M. Halford,
Maria L. Macheda,
Clare L. Parish,
Elena A. Takano,
Stephen B. Fox,
Daniel Layton,
Edouard C. Nice,
Steven A. Stacker
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0075447
Subject(s) - wnt signaling pathway , monoclonal antibody , microbiology and biotechnology , biology , neurite , wnt3a , receptor tyrosine kinase , phage display , antibody , signal transduction , biochemistry , genetics , in vitro
RYK is an unusual member of the receptor tyrosine kinase (RTK) family that is classified as a putative pseudokinase. RYK regulates fundamental biological processes including cell differentiation, migration and target selection, axon outgrowth and pathfinding by transducing signals across the plasma membrane in response to the high affinity binding of Wnt family ligands to its extracellular Wnt inhibitory factor (WIF) domain. Here we report the generation and initial characterization of a fully human inhibitory monoclonal antibody to the human RYK WIF domain. From a naïve human single chain fragment variable (scFv) phage display library, we identified anti-RYK WIF domain–specific scFvs then screened for those that could compete with Wnt3a for binding. Production of a fully human IgG 1κ from an inhibitory scFv yielded a monoclonal antibody that inhibits Wnt5a-responsive RYK function in a neurite outgrowth assay. This antibody will have immediate applications for modulating RYK function in a range of settings including development and adult homeostasis, with significant potential for therapeutic use in human pathologies.

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