Laboratory for the Analysis of Medicines (LAM), Department of Pharmacy, CIRM, University of Liège, 4000 Liège, Belgium; Analytical Chemistry and Drug Analysis Department, Faculty of Pharmacy, University of Medicine, Pharmacy, Sciences and Technology from Tîrgu Mureș, 540139 Tîrgu Mureș, Romania.
Laboratory for the Analysis of Medicines (LAM), Department of Pharmacy, CIRM, University of Liège, 4000 Liège, Belgium.
Talanta. 2019 Apr 1;195:668-675. doi: 10.1016/j.talanta.2018.11.050. Epub 2018 Dec 1.
Neutrophil gelatinase associated lipocalin (NGAL) is a protein that was found to be overexpressed in acute kidney injury (AKI). The rise in NGAL concentration, both in urine or plasma, appears earlier than for other classical renal function markers such as serum creatinine, thus making it a suitable marker for early pathology detection. The aim of this study was to develop a method involving tryptic digestion, solid phase extraction and LC-MS/MS analysis to analyze NGAL in plasma medium using an isotope labeled surrogate protein, containing NGAL signature tags, as internal standard (QPrEST). The method was validated for the analysis of NGAL in an analytical range from 50 to 1250 ng/mL using two different proteotypic peptides. The method was further used to quantify the NGAL in human plasma samples for whom elevated NGAL values were expected. NGAL values were between 190.8 and 242.6 ng/mL for control group and between 228.1 and 3526.2 ng/mL for patient group. This study proved that the selection of the right internal standard is of utmost importance in targeted proteomics studies as the digestion steps might cause high variability. This study also confirmed that, although NGAL is highly resistant to proteases such as trypsin, the method could be fully validated according to FDA guidelines and subsequently used to assess NGAL levels in patient plasma with high analytical confidence.
中性粒细胞明胶酶相关脂质运载蛋白(NGAL)是一种在急性肾损伤(AKI)中过度表达的蛋白质。NGAL 浓度的升高,无论是在尿液还是血浆中,都比其他经典的肾功能标志物(如血清肌酐)更早出现,因此它是早期病理检测的合适标志物。本研究旨在开发一种方法,该方法涉及胰蛋白酶消化、固相萃取和 LC-MS/MS 分析,使用含有 NGAL 特征标签的同位素标记替代蛋白作为内标(QPrEST)来分析血浆中的 NGAL。该方法使用两种不同的蛋白水解肽,在 50 至 1250ng/mL 的分析范围内进行了 NGAL 的验证。该方法还用于定量人血浆样品中的 NGAL,这些样品预计会出现 NGAL 值升高。对照组的 NGAL 值在 190.8 和 242.6ng/mL 之间,而患者组的 NGAL 值在 228.1 和 3526.2ng/mL 之间。本研究证明,在靶向蛋白质组学研究中,选择正确的内标至关重要,因为消化步骤可能会导致高度可变。本研究还证实,尽管 NGAL 对胰蛋白酶等蛋白酶具有高度抗性,但该方法可以根据 FDA 指南进行全面验证,并随后用于评估患者血浆中具有高分析可信度的 NGAL 水平。