A quantitative method for aquaporin-1 protein using magnetic preconcentration and probe-based immunoassay coupling to inductively coupled plasma mass spectrometry in urine analysis

Aquaporin-1 (AQP1) protein plays a crucial role in intracellular and extracellular water homeostasis and fluid transport in organs and tissues associated with diverse life activities and is extremely abundant in the kidney. Accurate detection of AQP1 in urine can be applied as screening of early-sta...

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Veröffentlicht in:Analytica chimica acta 2024-10, Vol.1324, p.343101, Article 343101
Hauptverfasser: Liang, Shuqi, Zhao, Shuang, Liu, Hongtao, Liu, Jiahui, Xie, Xiuqin, Chen, Ruohong, Chen, Baowei, Luan, Tiangang
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Sprache:eng
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Zusammenfassung:Aquaporin-1 (AQP1) protein plays a crucial role in intracellular and extracellular water homeostasis and fluid transport in organs and tissues associated with diverse life activities and is extremely abundant in the kidney. Accurate detection of AQP1 in urine can be applied as screening of early-stage disease. Application of magnetic preconcentration and probe-based signal amplification strategy coupling to inductively coupled plasma mass spectrometry (ICP-MS) is a more accurate, sensitive and specific detection method for AQP1 in complex biological samples compared to conventional methods. We described an element-labelling strategy based on magnetic preconcentration and probe-based immunoassay coupling to ICP-MS detection. The magnetic beads (MBs) modified with epoxy groups were capable of enriching AQP1 proteins and separating them from complex matrices. The probe constructed by conjugating anti-AQP1 antibody molecules on the surface of gold nanoparticles could specifically recognize AQP1 proteins attached on MBs and be analyzed by ICP-MS. The concentration of AQP1 protein could be precisely quantified and amplified by 14,000 times through the corresponding signal of Au atoms. This assay for AQP1 protein quantification achieved a detection limit down to 0.023 ng mL−1, a broad linear calibration curve between 0.3 ng mL−1 and 30 ng mL−1, as well as outstanding specificity. The proposed method was successfully applied to detect AQP1 protein in human urine samples, showing the potential for its applications concerning accurate AQP1 quantification. It can also screen a wide range of proteins provided the antibodies specific to these target proteins are available. [Display omitted] •AuNPs-based probe is endowed with signal amplification of Au element for target protein detection.•The method is integrated with magnetic preconcentration, probe-involved immunoassay, and ICP-MS analysis.•Magnetic preconcentration and AuNPs-labelling amplification allow for sensitive detection of AQP1 protein in urine samples.•The detection method is available for most proteins which have one antibody, not requiring antibody pairs.
ISSN:0003-2670
1873-4324
1873-4324
DOI:10.1016/j.aca.2024.343101