Conditional Binding of Arsenic Trioxide (ATO) to Cysteine-Rich Zinc Finger Motifs within RBCC Domain of PML Protein
The arsenic trioxide (ATO)-based cure of acute promyelocytic leukemia is attributed to PML/RARα oncoprotein degradation through binding of its RBCC domain (i.e., consist of RING, B-box1, B-box2, and Coiled-coil) with arsenic. Despite ATO being proven to interact with the Cysteine213 triad in the B-box2 trimer of PML-Nuclear Bodies, whether its direct binding to cysteine-rich zinc finger motifs in PML protein, remains unclear. Consequently, we purified the RING, B-box1, and B-box2 domains to assess their potential for arsenic-binding. The results showed that ATO cannot displace zinc ions under physiological conditions but binds with zinc finger domains under zinc-depletion in low-pH conditions, revealing a conditional binding mechanism.
Authors
- Yang Gao (ORCID: https://orcid.org/0000-0002-9068-9993)
- Hua Naranmandura (ORCID: https://orcid.org/0000-0003-0799-2340)
- Pei Han Yu
- Chen Zhu (ORCID: https://orcid.org/0000-0001-5302-1233)
- Yuan Yuan Kang (ORCID: https://orcid.org/0000-0002-2854-6246)
- Yuki Tanaka (ORCID: https://orcid.org/0000-0001-8298-7408)
- Yasumitsu Ogra (ORCID: https://orcid.org/0000-0002-8268-1828)
- Xin Wang (ORCID: https://orcid.org/0000-0002-8284-8640)
- Chang Yang (ORCID: https://orcid.org/0000-0002-7006-6377)
- Gaowa Wureng
Institutions
- Chiba University (JP)
- Zhejiang University (CN)
- Kumamoto University (JP)
Publication Details
- Journal
- Chemical Research in Toxicology
- Published
- 2025-04-12
- DOI
- https://doi.org/10.1021/acs.chemrestox.5c00087
- Citations
- 2
- Primary Topic
- Retinoids in leukemia and cellular processes
- Type
- article
- Field-Weighted Citation Impact
- 1.61