β-Cyclodextrin-Functionalized Mycobacterium smegmatis Porin A for Steroid Discrimination and Gut Metabolite Monitoring.
basic_science · Level V
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- Record sourced from PubMed, PMID 42584251.
- Also identified by DOI 10.1021/acs.nanolett.6c02204.
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Abstract
Steroid metabolites like estradiol (E2) and bile acids (BAs) play pivotal roles in human metabolism but are challenging to distinguish due to their high structural homology. Herein, we integrated β-cyclodextrin (βCD) into the MspA nanopore via a hetero-octameric assembly following Michael addition. This engineered sensor, termed MspA-βCD, affords precise control over βCD conformation within the pore lumen, positioning βCD proximal to the pore constriction zone to enhance sensing resolution. The platform achieves high-resolution discrimination of 11 structurally analogous steroid metabolites. Automated machine learning classification achieved 99.7% validation accuracy. Single-molecule evidence revealed three key structural factors that exert a pivotal influence on the dissociation rate constants of BA-βCD complexes: the chirality of the 7-hydroxyl group, steric hindrance of the 12-hydroxyl group, and side-chain conjugation pattern of BAs. The platform was successfully validated for bile acid profiling in real fecal samples, highlighting its potential for point-of-care diagnosis of metabolic disorders.
Medical subject headings
- beta-Cyclodextrins
- Porins
- Steroids
- Mycobacterium smegmatis
- Bile Acids and Salts