| Literature DB >> 31562851 |
Yanan Li1, Huoyan Ji1, Lei Shen1, Xiuying Shi1, Jianxin Wang2.
Abstract
Cystatin C is considered as an alternative to the evaluation of glomerular filtration rate. In this study, we highlighted an LC-MS/MS approach for the absolute quantitation of serum cystatin C based on label-free internal standards. A tryptic peptide (ALDFAVGEYNK) was selected as the surrogate whilst analogue (ALDFAVGEYQK) served as an internal standard. After denaturation, reduction, alkylation, digestion and concentration, the target peptides were separated on an LC column and monitored under MRM. The calibration range was from 0.25 mg/L to 15 mg/L with LLOQ of 0.05 mg/L and LOD of 0.03 mg/L, respectively. The certified reference material (ERM-DA471) was determined at 5.12 mg/L with bias of 6.57%. The recovery was between 89.68% and 92.43%. The RSD of intra- and inter-assay imprecision were both <10%. Good stability was also observed. The assay also demonstrated that the quantification of native cystatin C in human serum could be achieved using label-free internal standards. The assay was robust, cheap and sensitive.Entities:
Keywords: Cystatin C; LC-MS/MS; Label-free; Surrogate peptide
Year: 2019 PMID: 31562851 DOI: 10.1016/j.ab.2019.113451
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365