A Comparison of gel (Hydragel 30) and capillary (Capillarys III Tera) electrophoresis for the characterization of human serum proteins

Objectives: To compare gel (Hydrasys 2 from Sebia) and capillary (Capillarys III Tera, Sebia) electrophoresis for the characterization of human serum proteins. Design and methods: 304 sera tested by gel electrophoresis during 8 routine laboratory days were concurrently tested by capillary electropho...

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Bibliographic Details
Main Authors: Caturegli, P. (Author), Howard, B.M (Author), Kuh, A. (Author), Rezavi, L. (Author)
Format: Article
Language:English
Published: Elsevier B.V. 2021
Subjects:
Online Access:View Fulltext in Publisher
LEADER 02955nam a2200445Ia 4500
001 10.1016-j.plabm.2021.e00233
008 220427s2021 CNT 000 0 und d
020 |a 23525517 (ISSN) 
245 1 0 |a A Comparison of gel (Hydragel 30) and capillary (Capillarys III Tera) electrophoresis for the characterization of human serum proteins 
260 0 |b Elsevier B.V.  |c 2021 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1016/j.plabm.2021.e00233 
520 3 |a Objectives: To compare gel (Hydrasys 2 from Sebia) and capillary (Capillarys III Tera, Sebia) electrophoresis for the characterization of human serum proteins. Design and methods: 304 sera tested by gel electrophoresis during 8 routine laboratory days were concurrently tested by capillary electrophoresis. Gels were read by an experienced medical technologist while capillary profiles by a Sebia representative and the same technologist. Most sera (214 of 304, 70%) were also analyzed by immunofixation electrophoresis, used here as the gold standard to calculate sensitivity and specificity of the gel and capillary systems. Results: Gel and capillary estimated the concentration of albumin, gamma region, and M-spikes nearly perfectly, and that of beta, alpha-2, and alpha-1 regions with excellent correlation. The two systems classified concordantly 268 of 304 sera (88% agreement) as having no, one, or two M-spikes, but differed in the remaining 36 sera (12%). Gel electrophoresis correctly identified M-spikes in 82 of 112 sera that were shown to have monoclonal band(s) by immunofixation (73% sensitivity), and correctly did not reveal M-spikes in 97 of the 102 sera that had no immunofixation bands (95% specificity). Capillary achieved slightly higher sensitivity (85 of 112, 76%) and slightly lower specificity (94 of 102, 92%), but the two areas under the ROC curves were nearly identical at 0.84. Conclusions: Gel and capillary electrophoresis systems perform similarly to estimate the concentration of serum protein fractions and detect M-spikes. © 2021 The Author(s) 
650 0 4 |a albumin 
650 0 4 |a Article 
650 0 4 |a Capillary 
650 0 4 |a capillary electrophoresis 
650 0 4 |a Capillarys III tera 
650 0 4 |a concentration (parameter) 
650 0 4 |a controlled study 
650 0 4 |a Electrophoresis 
650 0 4 |a gel electrophoresis 
650 0 4 |a gold standard 
650 0 4 |a human 
650 0 4 |a human cell 
650 0 4 |a Hydrasys II 
650 0 4 |a immunoelectrophoresis 
650 0 4 |a medical technologist 
650 0 4 |a monoclonal spike 
650 0 4 |a paraprotein 
650 0 4 |a protein analysis 
650 0 4 |a protein electrophoresis 
650 0 4 |a Sebia 
650 0 4 |a sensitivity and specificity 
650 0 4 |a Serum proteins 
650 0 4 |a unclassified drug 
700 1 |a Caturegli, P.  |e author 
700 1 |a Howard, B.M.  |e author 
700 1 |a Kuh, A.  |e author 
700 1 |a Rezavi, L.  |e author 
773 |t Practical Laboratory Medicine