David Murray, Mindy Kohlhagen, Mark Martinez, James M. Larkin, Jon D. Coker, Angela Dispenzieri, Surendra Dasari, Melissa R. Snyder, Tax Kourelis, Anne E. Tebo, Patrick M. Vanderboom, Maria Alice V. Willrich
In 2018, the Mayo Clinic Protein Immunology Laboratory switched from immunofixation electrophoresis to a MALDI-TOF MS (Mass-Fix) method for the isotyping of M-proteins with a goal of replacing serum protein electrophoresis (SPEP) later. This study defines the performance characteristics of the MALDI-TOF MS method (Q-Mass-Fix) for simultaneous quantitation and isotyping of M-proteins in conjunction with immunoglobulin quantitation. Utilizing an in-house developed software, retrospective quantitation and isotyping by Q-Mass-Fix of 6395 SPEP M-protein positive samples demonstrated good correlation with >90% of results not needing manual intervention. The assay was linear over a range of 7.5 to 0.004 g/dL with 75% of M-proteins detected at 0.004 g/dL. Thus, Q-Mass-Fix quantitation was superior to our current agarose gel SPEP and suitable for patient care.