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Superresolution imaging of antibiotic-induced structural disruption of bacteria enabled by photochromic glycomicelles.
Hu, Xi-Le; Gan, Hui-Qi; Gui, Wen-Zhen; Yan, Kai-Cheng; Sessler, Jonathan L; Yi, Dong; Tian, He; He, Xiao-Peng.
Afiliación
  • Hu XL; Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, Ch
  • Gan HQ; Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, Ch
  • Gui WZ; Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, Ch
  • Yan KC; Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, Ch
  • Sessler JL; National Center for Liver Cancer, The International Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Shanghai 200438, China.
  • Yi D; Department of Chemistry, University of Bath, Bath BA2 7AY, United Kingdom.
  • Tian H; Department of Chemistry, The University of Texas at Austin, Austin, TX 78712-1224.
  • He XP; Research Center for Systems Biosynthesis, China State Institute of Pharmaceutical Industry, National Key Laboratory of Lead Druggability Research, Shanghai 201203, China.
Proc Natl Acad Sci U S A ; 121(37): e2408716121, 2024 Sep 10.
Article en En | MEDLINE | ID: mdl-39226360
ABSTRACT
Bacterial evolution, particularly in hospital settings, is leading to an increase in multidrug resistance. Understanding the basis for this resistance is critical as it can drive discovery of new antibiotics while allowing the clinical use of known antibiotics to be optimized. Here, we report a photoactive chemical probe for superresolution microscopy that allows for the in situ probing of antibiotic-induced structural disruption of bacteria. Conjugation between a spiropyran (SP) and galactose via click chemistry produces an amphiphilic photochromic glycoprobe, which self-assembles into glycomicelles in water. The hydrophobic inner core of the glycomicelles allows encapsulation of antibiotics. Photoirradiation then serves to convert the SP to the corresponding merocyanine (MR) form. This results in micellar disassembly allowing for release of the antibiotic in an on-demand fashion. The glycomicelles of this study adhere selectively to the surface of a Gram-negative bacterium through multivalent sugar-lectin interaction. Antibiotic release from the glycomicelles then induces membrane collapse. This dynamic process can be imaged in situ by superresolution spectroscopy owing to the "fluorescence blinking" of the SP/MR photochromic pair. This research provides a high-precision imaging tool that may be used to visualize how antibiotics disrupt the structural integrity of bacteria in real time.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Benzopiranos / Indoles / Antibacterianos Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Benzopiranos / Indoles / Antibacterianos Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2024 Tipo del documento: Article