MRS2 antibodies are primarily designed for detecting mitochondrial Mg transporters in mammals, yeast, or other model organisms. Key features include:
Species Specificity: Antibodies for mammalian MRS2 (e.g., Alomone ANT-148) show ~90–93% identity to mouse/rat orthologs but lack cross-reactivity with plant MRS2-4 .
Localization: MRS2 antibodies typically target mitochondrial matrix regions, contrasting with MRS2-4’s reported ER localization in Arabidopsis .
Functional Insights: Structural studies (e.g., human MRS2) reveal pentameric channels regulated by Mg²⁺/Ca²⁺, but analogous data for MRS2-4 are absent .
MRS2-4 is indispensable for Mg uptake and storage in Arabidopsis, as shown by phenotypic and physiological analyses:
| Parameter | Wild Type | MRS2-4 Mutant | Source |
|---|---|---|---|
| Mg Concentration (Normal Conditions) | ~2.5 µmol/g DW | ~1.8 µmol/g DW | |
| Growth Under Low Mg | Normal | Severe defects | |
| ER Localization | Confirmed | Confirmed |
Bi-directional Transport: MRS2-4 may mediate Mg influx/efflux, buffering cytosolic Mg via ER storage .
Redundancy: Double mutants (mrs2-4/mrs2-7) show exacerbated defects, indicating partial functional overlap .
Despite its importance, MRS2-4 remains understudied due to:
Low Sequence Homology: MRS2-4 shares minimal identity with mammalian MRS2 (e.g., human MRS2 vs. Arabidopsis MRS2-4: ~20–30% similarity).
Subcellular Localization: ER targeting complicates antibody design compared to mitochondrial MRS2 .
Research Focus: Existing studies prioritize mammalian/yeast MRS2, leaving plant homologs underexplored .
Custom Antibody Development: A plant-specific antibody would require immunogenic peptide design (e.g., targeting Arabidopsis-unique regions).
Functional Validation: Structural studies (e.g., cryo-EM) could elucidate MRS2-4’s Mg-binding sites and regulatory mechanisms .
Cross-Species Comparisons: Investigating whether mammalian MRS2 antibodies cross-react with MRS2-4 via epitope mapping.