1. ‘Shed’ furin: mapping of the cleavage determinants and identification of its C-terminus
- Author
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Plaimauer, B, Mohr, G, Wernhart, W, Himmelspach, M, Dorner, F, and Schlokat, U
- Subjects
Furin ,Molecular Sequence Data ,Cell Biology ,Arginine ,Transfection ,Biochemistry ,Mass Spectrometry ,Cell Line ,Protein Structure, Tertiary ,Mutagenesis, Site-Directed ,Serine ,Humans ,Amino Acid Sequence ,Subtilisins ,Molecular Biology ,Research Article ,Sequence Deletion - Abstract
The human endoprotease furin is involved in the proteolytic maturation of the precursor molecules of a wide variety of bioactive proteins. Despite its localization in the membranes of the trans-Golgi system by means of a transmembrane domain, it has repeatedly been reported to form a C-terminally truncated, naturally secreted form referred to as ‘shed’ furin. In order to identify the cleavage site, internal deletion mutants of increasing size, N-terminal to Leu708, and subsequently individual amino acid substitutions were introduced, and Arg683 was identified as the prime determinant for shedding. MS analysis determined Ser682 as the C-terminus of shed furin, suggesting that monobasic cleavage may occur N-terminal to Arg683. Alteration of Arg683 directs the shedding mechanism to alternative cleaving sites previously unused.
- Published
- 2001
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