Abstract

Mg2+ plays important roles in many physiological processes. However, the underlying molecular mechanisms, especially in the apoptotic pathway, remain unclear due to the diffusion of Mg2+ probes, which hinders long-term imaging in specific organelles. We developed an immobilized Mg2+ probe, MGH, which is covalently conjugated with the HaloTag protein in various organelles. HaloTag-coupled MGH enabled long-term imaging of intracellular local Mg2+ dynamics for 24 h. To exploit this remarkable property, MGH was applied to the investigation of intracellular Mg2+ dynamics during apoptosis. Time-lapse imaging revealed an increase in the Mg2+ concentration after apoptotic cell shrinkage. Combined imaging analyses of intracellular Mg2+ and ATP concentrations strongly suggested that this Mg2+ concentration increase was caused by the dissociation of Mg2+ from ATP, along with a decrease in the intracellular ATP concentration. Thus, this protein-coupled Mg2+ probe could be a new chemical tool to elucidate intracellular Mg2+ dynamics with high spatiotemporal resolution.

Highlights

  • Mg2+ is an essential divalent cation in cells, and the overall intracellular Mg2+ concentration ranges between 17 and 20 mM

  • We developed a novel Mg2+ probe, MGH, which covalently binds to HaloTag protein expressed in various cellular compartments

  • The conjugation of MGH to HaloTag dramatically suppressed the extracellular leakage of MGH, and the Mg2+ sensing ability of MGH was retained for 24 h. These noteworthy properties were successfully applied to long-term visualization of intracellular Mg2+ dynamics during apoptosis

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Summary

Introduction

Mg2+ is an essential divalent cation in cells, and the overall intracellular Mg2+ concentration ranges between 17 and 20 mM. Abnormal Mg2+ homeostasis is involved in several disorders including diabetes, hypertension, Parkinson’s disease, and cancer.[6,7]

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