4.7 Article

Engineering and Structural Characterization of a Linear Polyubiquitin-Specific Antibody

Journal

JOURNAL OF MOLECULAR BIOLOGY
Volume 418, Issue 3-4, Pages 134-144

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2011.12.053

Keywords

ubiquitin; linkage; phage display; immunoglobulin; X-ray crystallography

Funding

  1. National Institutes of Health, National Institute of General Medical Sciences
  2. Howard Hughes Medical Institute
  3. Office of Science, Office of Basic Energy Sciences, of U.S. Department of Energy [DE-AC02-05CH11231]

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Polyubiquitination is an essential posttranslational modification that plays critical roles in cellular signaling. PolyUb (polyubiquitin) chains are formed by linking the carboxyl-terminus of one Ub (ubiquitin) subunit to either a lysine residue or the amino-terminus of an adjacent Ub. Linkage through the amino-terminus results in linear polyubiquitination that has recently been demonstrated to be a key step in nuclear factor kappa B activation; however, tools to study linear chains have been lacking. We therefore engineered a linear-linkage-specific antibody that is functional in Western blot, immunoprecipitation, and immunofluorescence applications. A crystal structure of the linear-linkage-specific antibody Fab fragment in complex with linear diubiquitin provides molecular insight into the nature of linear chain specificity. We use the antibody to demonstrate that linear polyUb is up-regulated upon tumor necrosis factor a stimulation of cells, consistent with a critical role in nuclear factor kappa B signaling. This antibody provides an essential tool for further investigation of the function of linear chains. (C) 2011 Published by Elsevier Ltd.

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