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May 2, 20260 citations

A hydrophilic interaction liquid chromatography-tandem mass spectrometry method for the quantification of intracellular cystine and its application in cystinosis research.

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TVToon VerdonckKU LeuvenRSRoger Mora de la SernaAdvanced PharmaPAPatrick Augustijns

Key Points

  • The research aims to establish a reliable method for measuring intracellular cystine levels, particularly in cystinosis.
  • Developed a hydrophilic interaction liquid chromatography-tandem mass spectrometry method.
  • Applied the method to HEK293T cell models, using both knockout and wild-type cells.
  • Utilized N-ethylmaleimide to prevent cysteine oxidation during sample preparation.
  • Achieved a lower limit of quantification of 12.5 nM with high reliability (R² ≥ 0.9986).
  • Identified significantly higher intracellular cystine in CTNS-knockout cells compared to wild-type cells.
  • Restored cystine levels to normal with cysteamine treatment or lentiviral-mediated CTNS re-expression.

Abstract

≥ 0.9986) and a lower limit of quantification (LLOQ) of 12.5 nM, representing a > 8-fold improvement over reported reversed-phase LC methods. Addition of N-ethylmaleimide (NEM) prior to cell lysis effectively limited cysteine oxidation and maintained sample stability at 4 °C. Applicability was demonstrated in an isogenic laboratory HEK293T cell model, where CTNS-knockout (KO) cells exhibited significantly elevated intracellular cystine levels compared to wild-type (WT) cells. As additional controls, elevated levels were successfully restored following cysteamine treatment or lentiviral-vector (LV)-mediated CTNS protein re-expression. The developed method hence provides a sensitive and reliable analytical platform for in vitro evaluation of novel therapeutic strategies in cystinosis research.

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Cite This Study

Verdonck et al. (2026) studied this question.

synapsesocial.com/papers/69f5945c71405d493afff22ehttps://doi.org/10.1007/s00216-026-06526-x
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