Quantification of CSF cystatin C using liquid chromatography tandem mass spectrometry

Background Cystatin C (CST3), a ubiquitously expressed cysteine protease inhibitor, is implicated in several neurological diseases. Here, we have developed an accurate CST3 measurement system based on liquid chromatography tandem mass spectrometry (LC-MS/MS). Methods LC-MS/MS based measurement for CSF CST3 was validated by determination of assay precision, accuracy and recovery. The values were compared with those measured by immunoassay. Glycosylation of CST3 in CSF was analyzed by Western blotting and lectin blotting. Results Measuring standard CST3 by LC-MS/MS produced a linear standard curve that correlated with assigned values (r2 = 0.99). Both intra- and inter-assay variation was < 10%. Although showed a correlation, the average CST3 concentration measured by LC-MS/MS was significantly higher than that of immunoassay. Western blotting showed the presence of a 25 KDa species along with CST3 monomer (14 KDa) in CSF. The volume of 25 KDa species was decreased by deglycosylation. Lectin blotting revealed a 25 KDa glycosylated protein in sialidase-treated CSF, which was decreased by deglycosylation. However, deglycosylation did not alter CST3 concentration measured by immunoassay. Conclusions Our results suggest that LC-MS/MS-based CST3 measurement is a robust method with higher detection ability. Such method could be useful for the diagnosis and monitoring of neurological diseases.