Biomarker discovery by imaging mass spectrometry - Transthyretin is a biomarker for gentamicin-induced nephrotoxicity in rat

被引:100
作者
Meistermann, Helene
Norris, Jeremy L.
Aerni, Hans-Rudolf
Cornett, Dale S.
Friedlein, Arno
Erskine, Annette R.
Augustin, Angelique
Mudry, Maria Cristina De Vera
Ruepp, Stefan
Suter, Laura
Langen, Hanno
Caprioli, Richard M.
Ducret, Axel
机构
[1] F Hoffmann La Roche & Co Ltd, Roche Ctr Med Genom, Div Pharmaceut, CH-4070 Basel, Switzerland
[2] Vanderbilt Univ, Mass Spectrometry Res Ctr, Nashville, TN 37232 USA
关键词
D O I
10.1074/mcp.M500399-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Adverse drug effects are often associated with pathological changes in tissue. An accurate depiction of the undesired affected area, possibly supported by mechanistic data, is important to classify the effects with regard to relevance for human patients. MALDI imaging MS represents a new analytical tool to directly provide the spatial distribution and the relative abundance of proteins in tissue. Here we evaluate this technique to investigate potential toxicity biomarkers in kidneys of rats that were administered gentamicin, a well known nephrotoxicant. Differential analysis of the mass spectrum profiles revealed a spectral feature at 12,959 Da that strongly correlates with histopathology alterations of the kidney. We unambiguously identified this spectral feature as transthyretin (Ser(28)-Gln(146)) using an innovative combination of tissue microextraction and fractionation by reverse-phase liquid chromatography followed by a top-down tandem mass spectrometric approach. Our findings clearly demonstrate the emerging role of imaging MS in the discovery of toxicity biomarkers and in obtaining mechanistic insights concerning toxicity mechanisms.
引用
收藏
页码:1876 / 1886
页数:11
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