Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1222246 | Journal of Pharmaceutical and Biomedical Analysis | 2011 | 4 Pages |
Abstract
Haptoglobin is known to bind to hemoglobin during intravascular hemolysis. Membrane-immobilized anti-haptoglobin antibody, which was produced after antibody was isolated by non-denaturing two-dimensional electrophoresis, was transferred to a polyvinylidene difluoride membrane and was stained using Ponceau S. The proteins bound to the membrane-immobilized anti-haptoglobin antibody were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and matrix-assisted laser desorption ionization/time-of-flight mass spectrometry. Hemoglobin was specifically obtained when the membrane-immobilized anti-haptoglobin antibody was incubated with human serum obtained from hemolysis blood. Furthermore, hemoglobin in the flowing fluid was captured by the membrane-immobilized anti-haptoglobin antibody and analyzed directly. The results indicate that hemolysis can be examined by direct trapping and analysis of hemoglobin under physiological conditions.
Keywords
IEFMatrix-assisted laser desorption ionization/time-of-flight mass spectrometryTRISTEMEDCBBTFA2-DEPVDF2-Amino-2-hydroxymethyl-1,3-propanediolCoomassie Brilliant BlueTrifluoroacetic acidTwo-dimensional electrophoresisImmunoaffinityisoelectric focusingpolyvinylidene difluorideMALDI ToF MSMALDI-TOF MSHaptoglobinHemolysisHemoglobin
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Youji Shimazaki, Ayaka Kimura,