Trace component fishing strategy based on offline two-dimensional liquid chromatography combined with PRDX3-surface plasmon resonance for Uncaria alkaloids

The rapid screening of bioactive constituents within traditional Chinese medicine (TCM) presents a significant challenge to researchers. Prevailing strategies for the screening of active components in TCM often overlook trace components owing to their concealment by more abundant constituents. To address this limitation, a fishing strategy based on offline two-dimensional liquid chromatography (2D-LC) combined with surface plasmon resonance (SPR) was utilized to screen bioactive trace components targeting peroxiredoxin 3 (PRDX3), using <i>Uncaria</i> alkaloids (UAs) as a case study. Initially, an orthogonal preparative offline 2D-LC system combining a positively charged C<sub>18</sub> column and a conventional C<sub>18</sub> column under disparate mobile phase conditions was constructed. To fully reveal the trace alkaloids, 13 2D fractions of UAs were prepared, and their components were characterized using mass spectrometry (MS). Subsequently, employing PRDX3 as the targeting protein, a SPR-based screening approach was established and rigorously validated with geissoschizine methyl ether (GSM) serving as a positive control for binding. Employing this refined strategy, 29 candidate binding alkaloids were fished from the 13 2D fractions. Notably, combining offline 2D-LC with SPR increased the yield of candidate binding components from 10 to 29 when compared to SPR-based screening alone. Subsequent binding affinity assays confirmed that PRDX3 was a direct binding target for the 12 fished alkaloids, with isovallesiachotamine (IV), corynoxeine <i>N</i>-oxide (CO-N), and cadambine (CAD) demonstrating the highest affinity for PRDX3. Their interactions were further validated through molecular docking analysis. Subsequent intracellular H<sub>2</sub>O<sub>2</sub> measurement assays and transfection experiments confirmed that these three trace alkaloids enhanced PRDX3-mediated H<sub>2</sub>O<sub>2</sub> clearance. In conclusion, this study introduced an innovative strategy for the identification of active trace components in TCM. This approach holds promise for accelerating research on medicinal components within this field.

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Publication Details

Journal
Journal of Pharmaceutical Analysis
Published
2025-02-20
DOI
https://doi.org/10.1016/j.jpha.2025.101244
Citations
3
Primary Topic
Alkaloids: synthesis and pharmacology
Type
article
Field-Weighted Citation Impact
4.67
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article

Trace component fishing strategy based on offline two-dimensional liquid chromatography combined with PRDX3-surface plasmon resonance for Uncaria alkaloids

Wanying Wu, Yaowen Liu, Wenyong Wu, Yang Zhou et al.
3 citations
Journal of Pharmaceutical Analysis
Alkaloids: synthesis and pharmacology
4.67
article

Trace component fishing strategy based on offline two-dimensional liquid chromatography combined with PRDX3-surface plasmon resonance for Uncaria alkaloids

Wanying Wu, Yaowen Liu, Wenyong Wu, Yang Zhou, Hao Zhang, Xinqin Kong, Jinjun Hou, Ni Hui, Huali Long, Ye Lu, Lu Shen, Zijia Zhang, Sihan Chen, Cheng Luo
article en
3 citations

Abstract

The rapid screening of bioactive constituents within traditional Chinese medicine (TCM) presents a significant challenge to researchers. Prevailing strategies for the screening of active components in TCM often overlook trace components owing to their concealment by more abundant constituents. To address this limitation, a fishing strategy based on offline two-dimensional liquid chromatography (2D-LC) combined with surface plasmon resonance (SPR) was utilized to screen bioactive trace components targeting peroxiredoxin 3 (PRDX3), using <i>Uncaria</i> alkaloids (UAs) as a case study. Initially, an orthogonal preparative offline 2D-LC system combining a positively charged C<sub>18</sub> column and a conventional C<sub>18</sub> column under disparate mobile phase conditions was constructed. To fully reveal the trace alkaloids, 13 2D fractions of UAs were prepared, and their components were characterized using mass spectrometry (MS). Subsequently, employing PRDX3 as the targeting protein, a SPR-based screening approach was established and rigorously validated with geissoschizine methyl ether (GSM) serving as a positive control for binding. Employing this refined strategy, 29 candidate binding alkaloids were fished from the 13 2D fractions. Notably, combining offline 2D-LC with SPR increased the yield of candidate binding components from 10 to 29 when compared to SPR-based screening alone. Subsequent binding affinity assays confirmed that PRDX3 was a direct binding target for the 12 fished alkaloids, with isovallesiachotamine (IV), corynoxeine <i>N</i>-oxide (CO-N), and cadambine (CAD) demonstrating the highest affinity for PRDX3. Their interactions were further validated through molecular docking analysis. Subsequent intracellular H<sub>2</sub>O<sub>2</sub> measurement assays and transfection experiments confirmed that these three trace alkaloids enhanced PRDX3-mediated H<sub>2</sub>O<sub>2</sub> clearance. In conclusion, this study introduced an innovative strategy for the identification of active trace components in TCM. This approach holds promise for accelerating research on medicinal components within this field.

Journal of Pharmaceutical AnalysisVol. 15(9)
Nanjing University of Chinese Medicine (CN), Chinese Academy of Sciences (CN), Shanghai University of Traditional Chinese Medicine (CN), Shanghai Institute of Materia Medica (CN), University of Chinese Academy of Sciences (CN)
Life below water
Openalex Percentile: Top 7%
Alkaloids: synthesis and pharmacology
4.67
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