APA
Click to copy
Korwar, A. M., Vannuruswamy, G., Jagadeeshaprasad, M., Jayaramaiah, R., Bhat, S., Regin, B. S., … Kulkarni, M. (2015). Development of Diagnostic Fragment Ion Library for Glycated Peptides of Human Serum Albumin: Targeted Quantification in Prediabetic, Diabetic, and Microalbuminuria Plasma by Parallel Reaction Monitoring, SWATH, and MSE*. Molecular &Amp; Cellular Proteomics.
Chicago/Turabian
Click to copy
Korwar, Arvind M., G. Vannuruswamy, M. Jagadeeshaprasad, R. Jayaramaiah, Shweta Bhat, Bhaskaran S Regin, S. Ramaswamy, et al. “Development of Diagnostic Fragment Ion Library for Glycated Peptides of Human Serum Albumin: Targeted Quantification in Prediabetic, Diabetic, and Microalbuminuria Plasma by Parallel Reaction Monitoring, SWATH, and MSE*.” Molecular & Cellular Proteomics (2015).
MLA
Click to copy
Korwar, Arvind M., et al. “Development of Diagnostic Fragment Ion Library for Glycated Peptides of Human Serum Albumin: Targeted Quantification in Prediabetic, Diabetic, and Microalbuminuria Plasma by Parallel Reaction Monitoring, SWATH, and MSE*.” Molecular &Amp; Cellular Proteomics, 2015.
BibTeX Click to copy
@article{arvind2015a,
title = {Development of Diagnostic Fragment Ion Library for Glycated Peptides of Human Serum Albumin: Targeted Quantification in Prediabetic, Diabetic, and Microalbuminuria Plasma by Parallel Reaction Monitoring, SWATH, and MSE*},
year = {2015},
journal = {Molecular & Cellular Proteomics},
author = {Korwar, Arvind M. and Vannuruswamy, G. and Jagadeeshaprasad, M. and Jayaramaiah, R. and Bhat, Shweta and Regin, Bhaskaran S and Ramaswamy, S. and Giri, A. and Mohan, V. and Balasubramanyam, M. and Kulkarni, M.}
}
Human serum albumin is one of the most abundant plasma proteins that readily undergoes glycation, thus glycated albumin has been suggested as an additional marker for monitoring glycemic status. Hitherto, only Amadori-modified peptides of albumin were quantified. In this study, we report the construction of fragment ion library for Amadori-modified lysine (AML), N(ε)-(carboxymethyl)lysine (CML)-, and N(ε)-(carboxyethyl)lysine (CEL)-modified peptides of the corresponding synthetically modified albumin using high resolution accurate mass spectrometry (HR/AM). The glycated peptides were manually inspected and validated for their modification. Further, the fragment ion library was used for quantification of glycated peptides of albumin in the context of diabetes. Targeted Sequential Window Acquisition of all THeoretical Mass Spectra (SWATH) analysis in pooled plasma samples of control, prediabetes, diabetes, and microalbuminuria, has led to identification and quantification of 13 glycated peptides comprised of four AML, seven CML, and two CEL modifications, representing nine lysine sites of albumin. Five lysine sites namely K549, K438, K490, K88, and K375, were observed to be highly sensitive for glycation modification as their respective m/z showed maximum fold change and had both AML and CML modifications. Thus, peptides involving these lysine sites could be potential novel markers to assess the degree of glycation in diabetes.