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Chem Sci. 2018 Dec 17;10(6):1607-1618. doi: 10.1039/c8sc04397c. eCollection 2019 Feb 14.

Testosterone meets albumin - the molecular mechanism of sex hormone transport by serum albumins.

Author information

1
Department of Molecular Physiology and Biological Physics , University of Virginia , 1340 Jefferson Park Avenue , Charlottesville , VA 22908 , USA . Email: wladek@iwonka.med.virginia.edu ; Email: ivan_s@iwonka.med.virginia.edu.
2
Center for Structural Genomics of Infectious Diseases (CSGID) , University of Virginia , 1340 Jefferson Park Avenue , Charlottesville , VA 22908 , USA.
3
Department of Chemistry , University of Nebraska-Lincoln , Lincoln , Nebraska 68588 , USA . Email: dhage1@unl.edu.

Abstract

Serum albumin is the most abundant protein in mammalian blood plasma and is responsible for the transport of metals, drugs, and various metabolites, including hormones. We report the first albumin structure in complex with testosterone, the primary male sex hormone. Testosterone is bound in two sites, neither of which overlaps with the previously suggested Sudlow site I. We determined the binding constant of testosterone to equine and human albumins by two different methods: tryptophan fluorescence quenching and ultrafast affinity extraction. The binding studies and similarities between residues comprising the binding sites on serum albumins suggest that testosterone binds to the same sites on both proteins. Our comparative analysis of albumin complexes with hormones, drugs, and other biologically relevant compounds strongly suggests interference between a number of compounds present in blood and testosterone transport by serum albumin. We discuss a possible link between our findings and some phenomena observed in human patients, such as low testosterone levels in diabetic patients.

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