Carbon nanotubes degraded by neutrophil myeloperoxidase induce less pulmonary inflammation
We have shown previously that single-walled carbon nanotubes can be catalytically biodegraded over several weeks by the plant-derived enzyme, horseradish peroxidase 1 . However, whether peroxidase intermediates generated inside human cells or biofluids are involved in the biodegradation of carbon na...
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Published in | Nature nanotechnology Vol. 5; no. 5; pp. 354 - 359 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.05.2010
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | We have shown previously that single-walled carbon nanotubes can be catalytically biodegraded over several weeks by the plant-derived enzyme, horseradish peroxidase
1
. However, whether peroxidase intermediates generated inside human cells or biofluids are involved in the biodegradation of carbon nanotubes has not been explored. Here, we show that hypochlorite and reactive radical intermediates of the human neutrophil enzyme myeloperoxidase catalyse the biodegradation of single-walled carbon nanotubes
in vitro
, in neutrophils and to a lesser degree in macrophages. Molecular modelling suggests that interactions of basic amino acids of the enzyme with the carboxyls on the carbon nanotubes position the nanotubes near the catalytic site. Importantly, the biodegraded nanotubes do not generate an inflammatory response when aspirated into the lungs of mice. Our findings suggest that the extent to which carbon nanotubes are biodegraded may be a major determinant of the scale and severity of the associated inflammatory responses in exposed individuals.
A type of peroxidase enzyme found in certain white blood cells can degrade single-walled carbon nanotubes into products that do not cause inflammation in the lungs of mice, suggesting that the severity of toxic responses of carbon nanotubes may depend on the extent of its degradation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 V.E.K., N.V.K., B.F. and A.S. designed the experiments, analysed the data and wrote the manuscript. W.F., J.S. and N.V.K. performed the neutrophil-based experiments. B.L.A. and N.V.K. participated in spectroscopic studies. I.I.V. and A.K. performed ESR measurements and gel electrophoresis. E.R.K., A.R.M. and A.S. designed and performed the animal experiments and evaluated the data. N.Y. and J.K.S. performed the molecular modelling studies. J.F. and D.S. carried out the electron microscopic studies. P.G. synthesized fluorescence labelled nanotubes. J.C. and Y.V. carried out the Raman microscopic studies. N.A.B. and Y.Y.T. performed the mass spectrometric analysis. All co-authors discussed the results and approved the final version of the manuscript. Author contributions |
ISSN: | 1748-3387 1748-3395 1748-3395 |
DOI: | 10.1038/nnano.2010.44 |