NMR Spectroscopy of Native and in Vitro Tissues Implicates PolyADP Ribose in Biomineralization

Author:

Chow W. Ying1,Rajan Rakesh2,Muller Karin H.3,Reid David G.1,Skepper Jeremy N.3,Wong Wai Ching1,Brooks Roger A.2,Green Maggie4,Bihan Dominique5,Farndale Richard W.5,Slatter David A.5,Shanahan Catherine M.6,Duer Melinda J.1

Affiliation:

1. Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK.

2. Orthopaedic Research Unit, University of Cambridge, Addenbrooke’s Hospital, Cambridge CB2 0QQ, UK.

3. Department of Physiology, Development, and Neuroscience, University of Cambridge, Downing Site, Cambridge CB2 3DY, UK.

4. Central Biomedical Resources, University of Cambridge, School of Clinical Medicine, West Forvie Building, Forvie Site, Robinson Way, Cambridge CB2 0SZ, UK.

5. Department of Biochemistry, University of Cambridge, Downing Site, Cambridge CB2 1QW, UK.

6. British Heart Foundation Centre of Research Excellence, Cardiovascular Division, James Black Centre, King’s College London, 125 Coldharbour Lane, London SE5 9NU, UK

Abstract

Fundamentals of Bone Formation In vitro models can help guide research for tissue engineering or drug delivery, but the extent to which results from in vitro experiments may mimic in vivo ones will depend on the robustness of the model. For complex tissues like the extracellular matrix or bone, this means matching the chemical organization of the tissue at both the atomic scale and the structural level. Chow et al. (p. 742 ) used nuclear magnetic resonance (NMR) spectroscopy to analyze a sample on both these length scales. First an isotope-enriched mouse was produced to enhance the NMR signal. Samples from these mice were then used to study the extracellular matrix of developing bone and the calcification front during fetal bone growth.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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