Literature DB >> 9572312

Artefacts in HPLC detection of 3-nitrotyrosine in human brain tissue.

H Kaur1, L Lyras, P Jenner, B Halliwell.   

Abstract

An HPLC method was used for quantification of 3-nitrotyrosine (3-NT) in human postmortem brain tissue. A peak with similar retention time to 3-NT was detected in brain tissue from patients with Parkinson's disease, Huntington's chorea, multiple system atrophy, and Alzheimer's disease but not in control tissue. The peak was lost on reduction with dithionite, a criterion often used to identify 3-NT. Tissue from the same neurodegenerative diseases was analysed by HPLC using a photodiode array detector in series with an amperometric electrochemical detector, but the peak was found not to be 3-NT. The absorbance spectrum, fragmentation pattern on mass spectroscopy, and electrochemical profile of this peak do not match authentic 3-NT. A search of the mass spectroscopy databases failed to reveal its identity. The presence of this closely eluting, dithionite-reducible peak could confound analysis of human tissues for 3-NT. In vitro experiments showed that high concentrations of peroxynitrite were needed to achieve detectable levels of 3-NT in human brain tissue.

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Year:  1998        PMID: 9572312     DOI: 10.1046/j.1471-4159.1998.70052220.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  6 in total

1.  Quantification of 3-nitrotyrosine in biological tissues and fluids: generating valid results by eliminating artifactual formation.

Authors:  D Yi; B A Ingelse; M W Duncan; G A Smythe
Journal:  J Am Soc Mass Spectrom       Date:  2000-06       Impact factor: 3.109

2.  Analysis of free and protein-bound nitrotyrosine in human plasma by a gas chromatography/mass spectrometry method that avoids nitration artifacts.

Authors:  M T Frost; B Halliwell; K P Moore
Journal:  Biochem J       Date:  2000-02-01       Impact factor: 3.857

Review 3.  Measuring reactive species and oxidative damage in vivo and in cell culture: how should you do it and what do the results mean?

Authors:  Barry Halliwell; Matthew Whiteman
Journal:  Br J Pharmacol       Date:  2004-05       Impact factor: 8.739

4.  Denitration of peroxynitrite-treated proteins by 'protein nitratases' from rat brain and heart.

Authors:  W N Kuo; R N Kanadia; V P Shanbhag; R Toro
Journal:  Mol Cell Biochem       Date:  1999-11       Impact factor: 3.396

5.  Electrochemical analysis of protein nitrotyrosine and dityrosine in the Alzheimer brain indicates region-specific accumulation.

Authors:  K Hensley; M L Maidt; Z Yu; H Sang; W R Markesbery; R A Floyd
Journal:  J Neurosci       Date:  1998-10-15       Impact factor: 6.167

6.  Analysis of peptides and proteins containing nitrotyrosine by matrix-assisted laser desorption/ionization mass spectrometry.

Authors:  A Sarver; N K Scheffler; M D Shetlar; B W Gibson
Journal:  J Am Soc Mass Spectrom       Date:  2001-04       Impact factor: 3.262

  6 in total

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