Liquid Chromatography-High Resolution Mass Spectrometry Analysis of Platelet Frataxin as a Protein Biomarker for the Rare Disease Friedreich’s Ataxia

• Published in: Analytical chemistry (Washington) Vol. 90; no. 3; pp. 2216 - 2223
• Main Authors: Guo, Lili, Wang, Qingqing, Weng, Liwei, Hauser, Lauren A, Strawser, Cassandra J, Rocha, Agostinho G, Dancis, Andrew, Mesaros, Clementina, Lynch, David R, Blair, Ian A
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 06.02.2018
• Subjects: Adolescent; Adult; Assaying; Ataxia; Biomarkers; Biomarkers - blood; Blood platelets; Blood Platelets - chemistry; Chemistry; Child; Chromatography; Chromatography, Liquid - methods; Dilution; Dimensional stability; Erythrocytes; Female; Frataxin; Friedreich Ataxia - diagnosis; Friedreich's ataxia; Gene expression; High performance liquid chromatography; Humans; Iron-Binding Proteins - blood; Liquid chromatography; Male; Mass spectrometry; Mass Spectrometry - methods; Mass spectroscopy; Middle Aged; Mitochondria; Platelets; Proteins; Rare Diseases - diagnosis; Sensitivity and Specificity; Spectroscopy; Stable isotopes; Therapeutic applications; Young Adult
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.7b04590

Friedreich’s ataxia (FA) is an autosomal recessive disease caused by an intronic GAA triplet expansion in the FXN gene, leading to reduced expression of the mitochondrial protein frataxin. FA is estimated to affect 1 in 50 000 with a mean age of death in the fourth decade of life. There are no approved treatments for FA, although experimental approaches, which involve up-regulation or replacement of frataxin protein, are being tested. Frataxin is undetectable in serum or plasma, and whole blood cannot be used because it is present in long-lived erythrocytes. Therefore, an assay was developed for analyzing frataxin in platelets, which have a half-life of 10 days. The assay is based on stable isotope dilution immunopurification two-dimensional nano-ultra high performance liquid chromatography/parallel reaction monitoring/mass spectrometry. The lower limit of quantification was 0.078 pg frataxin/μg protein, and the assay had 100% sensitivity and specificity for discriminating between controls and FA cases. The mean levels of control and FA platelet frataxin were 9.4 ± 2.6 and 2.4 ± 0.6 pg/μg protein, respectively. The assay should make it possible to rigorously monitor the effects of therapeutic interventions on frataxin expression in this devastating disease.