AHR is a member of the basic helix-loop-helix/PER-ARNT-SIM (bHLH/PAS) transcription factor family. It binds planar aromatic hydrocarbons like 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), triggering nuclear translocation and heterodimerization with ARNT (AhR nuclear translocator) to regulate genes such as CYP1A1 . Antibodies targeting AHR are indispensable tools for detecting its expression, activation state, and interactions in cellular and tissue contexts.
Xenobiotic Metabolism: Activates cytochrome P450 enzymes (e.g., CYP1A1) to metabolize environmental toxins .
Immune Regulation: Modulates PD-L1 expression in non-small cell lung cancer (NSCLC), influencing immunotherapy response .
Cell Cycle and Apoptosis: Interacts with E2F1 to suppress TP73 and Apaf1, blocking apoptosis .
Western Blot (WB): Detects AHR at ~96–110 kDa in human, mouse, and rat tissues .
Immunohistochemistry (IHC): Localizes AHR in paraffin-embedded brain tissues (rat/mouse) .
Chromatin Immunoprecipitation (ChIP): Identifies AHR binding to the PD-L1 promoter .
Immunoprecipitation (IP): Studies AHR-HSP90 complexes in cytoplasmic/nuclear fractions .
Nuclear AHR (AhR N) combined with membranous PD-L1 (PD-L1 M) predicts improved progression-free survival (PFS) in NSCLC patients treated with immune checkpoint inhibitors (ICIs) .
Hazard Ratios: AhR NPD-L1 M (HR: 0.0831) outperforms PD-L1 alone (HR: 0.226) .
Mechanism: AHR directly binds the PD-L1 promoter, driving transcription .
CK2 Phosphorylation: ARNT isoform 1 phosphorylation at S77 enhances AHR target gene expression (e.g., CYP1A1), a process dependent on AhR ligand activation .
Biomarker Potential: AhR NPD-L1 M status is a cost-effective biomarker for ICI response .
Specificity: MA1-514 detects AHR in wild-type HeLa cells but not AHR-knockout lines .
Cross-Reactivity: Clone 17840-1-AP validates across human, mouse, and rat samples .
| Antibody | Calculated MW | Observed MW |
|---|---|---|
| 17840-1-AP | 96 kDa | 105–110 kDa |
| NB100-2289 | 90–105 kDa | 74 kDa (Simple Western) |
Note: Discrepancies arise from post-translational modifications .