Cholesterol-dependent enzyme activity of human TSPO1
Abstract
The amino acid sequence of the tryptophan-rich sensory proteins (TSPO) is substantially conserved throughout all kingdoms of life. Human mitochondrial TSPO1 ( Hs TSPO1) binds to porphyrins and steroids, although its interactions with these molecules remains unknown. Hs TSPO1 is associated with numerous physiological and pathological disorders, but the underlying molecular mechanisms are unknown. Here, we disclose the finding of human mitochondrial TSPO as a cholesterol-dependent protoporphyrin IX oxygenase. The results of our biochemical characterization are consistent with structural data and evolutionary analysis. The dependence of Hs TSPO1 activity on cholesterol may be the result of the coevolution of this membrane protein with the membrane system. Our study provides a molecular foundation for comprehending the various roles played by mitochondrial TSPO in normal physiological and pathological situations.
Article Details
Journal Info
Proceedings of the National Academy of Sciences
National Academy of Sciences
Authors (8)
Weihua Qiu
Key Laboratory of Molecule Synthesis and Function Discovery, Fujian Province University, College of Chemistry, State Key Laboratory of Green and Efficient Development of Phosphorus Resources
Thi Kim Hoang Trinh
Department of Medicinal Chemistry, Virginia Commonwealth University
Claudio Catalano
Department of Medicinal Chemistry, Virginia Commonwealth University
Akul Mehta
Department of Medicinal Chemistry, Virginia Commonwealth University
Umesh R. Desai
Department of Medicinal Chemistry, Virginia Commonwealth University
Glen E. Kellogg
Department of Medicinal Chemistry, Virginia Commonwealth University
Wayne A. Hendrickson
Department of Biochemistry and Molecular Biophysics, Columbia University
Youzhong Guo
Department of Medicinal Chemistry, Virginia Commonwealth University