The Proteomic Analysis of Pancreatic Exocrine Insufficiency Protein Marker in Type 2 Diabetes Mellitus Patients

International Conference on Chemistry and Material Science 2017

化学;材料科学

Srihardyastutie, Arie^1 ; Soeatmadji, D.W.^2 ; Fatchiyah^3 ; Aulanni'Am^1

Chemistry Department, Faculty of Science, Brawijaya University, Indonesia^1

Medical Faculty of Brawijaya University, Indonesia^2

Biology Department, Faculty of Science, Brawijaya University, Indonesia^3

关键词: marker;    Methyltransferases;    Negative control;    pancreatic exocrine;    Pathogenic mechanisms;    Peptide fragments;    Proteomic analysis;    Type 2 diabetes mellitus;   

Others  :  https://iopscience.iop.org/article/10.1088/1757-899X/299/1/012021/pdf
DOI  :  10.1088/1757-899X/299/1/012021

学科分类：材料科学（综合）

来源: IOP

【 摘 要 】

Type 2 Diabetes Mellitus (T2D) is the vast majority case of diabetes. Patient with T2D is at higher risk for developing acute or chronic pancreatitis. Prolonged hyperglycemia results in damages to tissue, which also causes dysfunctions of some organ systems, including enzyme or hormone secretions. Commonly, dysfunction or insufficiency of pancreatic exocrine is evaluated by increasing activity of serum pancreatic enzyme, such as amylase and lipase. Although incidence of pancreatitis was found in Indonesian T2D, the pathogenic mechanism still unclear. The aim of this study was to characterize the marker protein that indicated the correlation of pancreatic exocrine insufficiency with progression of T2D. Proteomic analysis using LC-MS/MS was used in identification and characterization of protein marker which indicates insufficiency pancreatic exocrine. First step, protein profile was analyzed by SDS-PAGE methods using serum sample of T2D compared with normal or healthy control, as negative control, and pancreatitis patients, as positive control. Protein with 18 kDa was found as a candidate protein marker which indicated the pancreatic exocrine insufficiency in T2D. The further identification of that protein using LC-MS/MS showed 4 peptide fragments. In silico analysis of the peptide fragment indicated the correlation of pancreatic exocrine insufficiency with progression of T2D was METTL10 - methyltransferase like protein-10.