Low Resolution Structure Determination Shows Procollagen C-Proteinase Enhancer to be an Elongated Multidomain Glycoprotein
pmid: 12486138
Low Resolution Structure Determination Shows Procollagen C-Proteinase Enhancer to be an Elongated Multidomain Glycoprotein
Procollagen C-proteinase enhancer (PCPE) is an extracellular matrix glycoprotein that can stimulate the action of tolloid metalloproteinases, such as bone morphogenetic protein-1, on a procollagen substrate, by up to 20-fold. The PCPE molecule consists of two CUB domains followed by a C-terminal NTR (netrin-like) domain. In order to obtain structural insights into the function of PCPE, the recombinant protein was characterized by a range of biophysical techniques, including analytical ultracentrifugation, transmission electron microscopy, and small angle x-ray scattering. All three approaches showed PCPE to be a rod-like molecule, with a length of approximately 150 A. Homology modeling of both CUB domains and the NTR domain was consistent with the low-resolution structure of PCPE deduced from the small angle x-ray scattering data. Comparison with the low-resolution structure of the procollagen C-terminal region supports a recently proposed model (Ricard-Blum, S., Bernocco, S., Font, B., Moali, C., Eichenberger, D., Farjanel, J., Burchardt, E. R., van der Rest, M., Kessler, E., and Hulmes, D. J. S. (2002) J. Biol. Chem. 277, 33864-33869) for the mechanism of action of PCPE.
- Deutsches Elektronen-Synchrotron DESY Germany
- University of Wisconsin System United States
- University of Wisconsin–Oshkosh United States
- Grenoble Alpes University France
- Institut de Recherche Interdisciplinaire de Grenoble France
MESH: Extracellular Matrix Proteins, Models, Molecular, 570, MESH: Microscopy, Protein Conformation, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Sequence Data, MESH: Glycoproteins, MESH: Amino Acid Sequence, Electron, Mass Spectrometry, Cell Line, MESH: Recombinant Proteins, MESH: X-Rays, MESH: Protein Conformation, MESH: Models, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, Humans, Scattering, Radiation, MESH: Sequence Homology, Amino Acid Sequence, Molecular Biology, Glycoproteins, MESH: Mass Spectrometry, info:eu-repo/classification/ddc/570, Extracellular Matrix Proteins, MESH: Humans, MESH: Molecular Sequence Data, Radiation, Sequence Homology, Amino Acid, X-Rays, MESH: Ultracentrifugation, Molecular, 540, Recombinant Proteins, MESH: Cell Line, Protein Structure, Tertiary, MESH: Protein Structure, Amino Acid, Microscopy, Electron, MESH: Scattering, Ultracentrifugation, Tertiary
MESH: Extracellular Matrix Proteins, Models, Molecular, 570, MESH: Microscopy, Protein Conformation, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Sequence Data, MESH: Glycoproteins, MESH: Amino Acid Sequence, Electron, Mass Spectrometry, Cell Line, MESH: Recombinant Proteins, MESH: X-Rays, MESH: Protein Conformation, MESH: Models, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, Humans, Scattering, Radiation, MESH: Sequence Homology, Amino Acid Sequence, Molecular Biology, Glycoproteins, MESH: Mass Spectrometry, info:eu-repo/classification/ddc/570, Extracellular Matrix Proteins, MESH: Humans, MESH: Molecular Sequence Data, Radiation, Sequence Homology, Amino Acid, X-Rays, MESH: Ultracentrifugation, Molecular, 540, Recombinant Proteins, MESH: Cell Line, Protein Structure, Tertiary, MESH: Protein Structure, Amino Acid, Microscopy, Electron, MESH: Scattering, Ultracentrifugation, Tertiary
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