Abstract
The molecular weights of plasma proteins from healthy subjects and from patients with well-or badly-controlled diabetes mellitus have been determined by use of a matrix-assisted laser desorption ionization method, representing a highly accurate technique for the determination of the molecular weight of large biomolecules. Using this approach, different molecular weights of human serum albumin have been found for healthy (66,572-66,694 dalton) and diabetic (66,785-68,959 dalton) subjects. Such differences can be rationalized as being due to the different number of glucose molecules condensed on the protein and/or their further oxidation products; in the case of our diabetic patients this number is in the range of 1.4-14.8. The data show the high validity and specificity of the technique, which allows us to evaluate, without any protein degradation procedure, the number of glucose molecules condensed on a specific protein and ascertain the relationship of this number to the physiopathogenetic conditions of the subjects studied. © 1995 Springer-Verlag.
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Lapolla, A., Fedele, D., Seraglia, R., Catinella, S., Baldo, L., Aronica, R., & Traldi, P. (1995). A new effective method for the evaluation of glycated intact plasma proteins in diabetic subjects. Diabetologia, 38(9), 1076–1081. https://doi.org/10.1007/BF00402178
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