Skip to main content
Top
Published in: Journal of Inherited Metabolic Disease 6/2011

01-12-2011 | Alkaptonuria

Collagen atomic scale molecular disorder in ochronotic cartilage from an alkaptonuria patient, observed by solid state NMR

Authors: Wing Ying Chow, Adam M. Taylor, David G. Reid, James A. Gallagher, Melinda J. Duer

Published in: Journal of Inherited Metabolic Disease | Issue 6/2011

Login to get access

Abstract

In pilot studies of the usefulness of solid state nuclear magnetic resonance spectroscopy in characterizing chemical and molecular structural effects of alkaptonuria on connective tissue, we have obtained 13 C spectra from articular cartilage from an AKU patient. An apparently normal anatomical location yielded a cross polarization magic angle spinning spectrum resembling literature spectra and dominated by collagen and glycosaminoglycan signals. All spectral linewidths from strongly pigmented ochronotic cartilage however were considerably increased relative to the control indicating a marked increase in collagen molecular disorder. This disordering of cartilage structural protein parallels, at the atomic level, the disordering revealed at higher length scales by microscopy. We also demonstrate that the abnormal spectra from ochronotic cartilage fit with the abnormality in the structure of collagen fibres at the ultrastructural level, whereby large ochronotic deposits appear to alter the structure of the collagen fibre by invasion and cross linking. Summary: Increased signal linewidths in solid state NMR spectra of ochronotic articular cartilage from an AKU patient relative to linewidths in normal, control, cartilage reveals a marked decrease in collagen molecular order in the diseased tissue. This atomic level disordering parallels higher length scale disorder revealed by microscopic techniques.
Literature
go back to reference Aliev AE (2005) Solid-state NMR studies of collagen-based parchments and gelatin. Biopolym 77:230–245CrossRef Aliev AE (2005) Solid-state NMR studies of collagen-based parchments and gelatin. Biopolym 77:230–245CrossRef
go back to reference Duer MJ (2004) Introduction to solid-state NMR spectroscopy. Blackwell Science, Oxford Duer MJ (2004) Introduction to solid-state NMR spectroscopy. Blackwell Science, Oxford
go back to reference Duer MJ, Friscic T, Murray RC, Reid DG, Wise ER (2009) The mineral phase of calcified cartilage: its molecular structure and interface with the organic matrix. Biophys J 96:3372–3378PubMedCrossRef Duer MJ, Friscic T, Murray RC, Reid DG, Wise ER (2009) The mineral phase of calcified cartilage: its molecular structure and interface with the organic matrix. Biophys J 96:3372–3378PubMedCrossRef
go back to reference Helliwell TR, Gallagher JA, Ranganath L (2008) Alkaptonuria - a review of surgical and autopsy pathology. Histopathol 53:503–512 Helliwell TR, Gallagher JA, Ranganath L (2008) Alkaptonuria - a review of surgical and autopsy pathology. Histopathol 53:503–512
go back to reference Huster D, Naji L, Schiller J, Arnold K (2004) Dynamics of the biopolymers in articular cartilage studied by magic angle spinning NMR. App Magn Reson 27:471–487CrossRef Huster D, Naji L, Schiller J, Arnold K (2004) Dynamics of the biopolymers in articular cartilage studied by magic angle spinning NMR. App Magn Reson 27:471–487CrossRef
go back to reference Martin RW, Zilm KW (2003) Preparation of protein nanocrystals and their characterization by solid state NMR. J Magn Reson 165:162–174PubMedCrossRef Martin RW, Zilm KW (2003) Preparation of protein nanocrystals and their characterization by solid state NMR. J Magn Reson 165:162–174PubMedCrossRef
go back to reference Middleton DA (2009) In: Harris RK, Wasylishen RE, Duer MJ (eds) Structural Biology in NMR Crystallography. Wiley, Chichester Middleton DA (2009) In: Harris RK, Wasylishen RE, Duer MJ (eds) Structural Biology in NMR Crystallography. Wiley, Chichester
go back to reference Naji L, Kaufmann J, Huster D, Schiller J, Arnold K (2000) C-13 NMR relaxation studies on cartilage and cartilage components. Carbohydr Res 327:439–446PubMedCrossRef Naji L, Kaufmann J, Huster D, Schiller J, Arnold K (2000) C-13 NMR relaxation studies on cartilage and cartilage components. Carbohydr Res 327:439–446PubMedCrossRef
go back to reference Schiller J, Naji L, Huster D, Kaufmann J, Arnold K (2001) H-1 and C-13 HR-MAS NMR investigations on native and enzymatically digested bovine nasal cartilage. Magn Reson Mater Phys Biol Med 13:19–27CrossRef Schiller J, Naji L, Huster D, Kaufmann J, Arnold K (2001) H-1 and C-13 HR-MAS NMR investigations on native and enzymatically digested bovine nasal cartilage. Magn Reson Mater Phys Biol Med 13:19–27CrossRef
go back to reference Taylor AM, Wlodarski B, Prior IA, Wilson PJM, Jarvis JC, Ranganath LR, Gallagher JA (2010) Ultrastructural examination of tissue in a patient with alkaptonuric arthropathy reveals a distinct pattern of binding of ochronotic pigment. Rheumatol 49:1412–1414CrossRef Taylor AM, Wlodarski B, Prior IA, Wilson PJM, Jarvis JC, Ranganath LR, Gallagher JA (2010) Ultrastructural examination of tissue in a patient with alkaptonuric arthropathy reveals a distinct pattern of binding of ochronotic pigment. Rheumatol 49:1412–1414CrossRef
Metadata
Title
Collagen atomic scale molecular disorder in ochronotic cartilage from an alkaptonuria patient, observed by solid state NMR
Authors
Wing Ying Chow
Adam M. Taylor
David G. Reid
James A. Gallagher
Melinda J. Duer
Publication date
01-12-2011
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 6/2011
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-011-9373-x

Other articles of this Issue 6/2011

Journal of Inherited Metabolic Disease 6/2011 Go to the issue