Fluor NMR study of amino acid derived ligand to study TSPO

Translocator protein (TSPO, 18 kDa), previously known as peripheral-type benzodiazepine receptor, is an evolutionarily conserved membrane protein involved in various physiological processes and patho-physiological conditions. The endogeneous TSPO ligand is a polypeptide of 9 kDa, but dipeptides with biological activity have been previously synthesized and characterized. Herein, we synthesized a phenyl alanine derived ligand with a <sup>19</sup>F labelling which opens prospective for <sup>19</sup>F-MRI and potential <sup>18</sup>F-PET applications. We characterized the coexistence of two conformers that are not equally sensitive to the media used for membrane protein studies. Interaction studies with the recombinant mouse TSPO (mTSPO) in different membrane-mimicking environments are presented using <sup>19</sup>F NMR enabling structure/function characterizations. A change in the mTSPO environment from pure detergent to lipid/detergent mixture reveals different exchange rates between bound and free ligand forms. Competition experiments with the high-affinity drug ligand (R)-PK 11195 suggests that phenyl alanine derived ligand binds in the same protein cavity.

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Publication Details

Journal
Biochimie
Published
2025-02-04
DOI
https://doi.org/10.1016/j.biochi.2025.01.015
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Fluor NMR study of amino acid derived ligand to study TSPO

Agathe Martinez, Frédéric Bihel, J Lacapère, Luminita Duma et al.
Biochimie
Chemical Synthesis and Reactions
article

Fluor NMR study of amino acid derived ligand to study TSPO

Agathe Martinez, Frédéric Bihel, J Lacapère, Luminita Duma, Cathy Hachet, Séverine Schneider
article en

Abstract

Translocator protein (TSPO, 18 kDa), previously known as peripheral-type benzodiazepine receptor, is an evolutionarily conserved membrane protein involved in various physiological processes and patho-physiological conditions. The endogeneous TSPO ligand is a polypeptide of 9 kDa, but dipeptides with biological activity have been previously synthesized and characterized. Herein, we synthesized a phenyl alanine derived ligand with a <sup>19</sup>F labelling which opens prospective for <sup>19</sup>F-MRI and potential <sup>18</sup>F-PET applications. We characterized the coexistence of two conformers that are not equally sensitive to the media used for membrane protein studies. Interaction studies with the recombinant mouse TSPO (mTSPO) in different membrane-mimicking environments are presented using <sup>19</sup>F NMR enabling structure/function characterizations. A change in the mTSPO environment from pure detergent to lipid/detergent mixture reveals different exchange rates between bound and free ligand forms. Competition experiments with the high-affinity drug ligand (R)-PK 11195 suggests that phenyl alanine derived ligand binds in the same protein cavity.

BiochimieVol. 233
Centre National de la Recherche Scientifique (FR), Chimie ParisTech - PSL (FR), Université Paris Sciences et Lettres (FR), Sorbonne Université (FR), Laboratoire d'Innovation Thérapeutique (FR), Institut Polytechnique de Bordeaux (FR), Laboratoire des Biomolécules (FR), Université de Strasbourg (FR), Université de Reims Champagne-Ardenne (FR)
Université de Strasbourg, Centre National de la Recherche Scientifique, Université de Reims Champagne-Ardenne, Sorbonne Université
Openalex Percentile: Top 98%
Chemical Synthesis and Reactions
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