Cholesterol-dependent enzyme activity of human TSPO1

The amino acid sequence of the tryptophan-rich sensory proteins (TSPO) is substantially conserved throughout all kingdoms of life. Human mitochondrial TSPO1 (<i>Hs</i>TSPO1) binds to porphyrins and steroids, although its interactions with these molecules remains unknown. <i>Hs</i>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 <i>Hs</i>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.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-03-27
DOI
https://doi.org/10.1073/pnas.2323045122
Citations
4
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
3.22

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article

Cholesterol-dependent enzyme activity of human TSPO1

Glen E. Kellogg, Wayne A. Hendrickson, Umesh R. Desai, Thi Kim Hoang Trinh et al.
4 citations
Proceedings of the National Academy of Sciences
Mitochondrial Function and Pathology
3.22
article

Cholesterol-dependent enzyme activity of human TSPO1

Glen E. Kellogg, Wayne A. Hendrickson, Umesh R. Desai, Thi Kim Hoang Trinh, Weihua Qiu, Youzhong Guo, Claudio Catalano, Akul Y. Mehta
article en
4 citations

Abstract

The amino acid sequence of the tryptophan-rich sensory proteins (TSPO) is substantially conserved throughout all kingdoms of life. Human mitochondrial TSPO1 (<i>Hs</i>TSPO1) binds to porphyrins and steroids, although its interactions with these molecules remains unknown. <i>Hs</i>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 <i>Hs</i>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.

Proceedings of the National Academy of SciencesVol. 122(13)
Virginia Commonwealth University (US), New York Structural Biology Center (US), Columbia University (US)
Office of Extramural Research, National Institutes of Health
Life in Land
Openalex Percentile: Top 9%
Mitochondrial Function and Pathology
3.22
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Cholesterol-dependent enzyme activity of human TSPO1 — Glen E. Kellogg, Wayne A. Hendrickson, et al. · Proceedings of the National Academy of Sciences (2025) | TGRS Research Map | TGRS