Your browser doesn't support javascript.
loading
BODIPY-Based Analogue of the TREM2-Binding Molecular Adjuvant Sulfavant A, a Chemical Tool for Imaging and Tracking Biological Systems.
Fioretto, Laura; Gallo, Carmela; Mercogliano, Marcello; Ziaco, Marcello; Nuzzo, Genoveffa; d'Ippolito, Giuliana; Follero, Olimpia; DellaGreca, Marina; Giaccio, Paolo; Nittoli, Valeria; Ambrosino, Concetta; Sordino, Paolo; Soluri, Alessandro; Soluri, Andrea; Massari, Roberto; D'Amelio, Marcello; De Palma, Raffaele; Fontana, Angelo; Manzo, Emiliano.
Afiliação
  • Fioretto L; Institute of Biomolecular Chemistry (CNR), Via Campi Flegrei 34, 80078 Pozzuoli, Napoli , Italy.
  • Gallo C; Institute of Biomolecular Chemistry (CNR), Via Campi Flegrei 34, 80078 Pozzuoli, Napoli , Italy.
  • Mercogliano M; Institute of Biomolecular Chemistry (CNR), Via Campi Flegrei 34, 80078 Pozzuoli, Napoli , Italy.
  • Ziaco M; Department of Chemical Sciences, University of Naples Federico II, Via Cinthia 4, 80136 Napoli, Italy.
  • Nuzzo G; Institute of Biomolecular Chemistry (CNR), Via Campi Flegrei 34, 80078 Pozzuoli, Napoli , Italy.
  • d'Ippolito G; Institute of Biomolecular Chemistry (CNR), Via Campi Flegrei 34, 80078 Pozzuoli, Napoli , Italy.
  • Follero O; Institute of Biomolecular Chemistry (CNR), Via Campi Flegrei 34, 80078 Pozzuoli, Napoli , Italy.
  • DellaGreca M; Institute of Biomolecular Chemistry (CNR), Via Campi Flegrei 34, 80078 Pozzuoli, Napoli , Italy.
  • Giaccio P; Department of Chemical Sciences, University of Naples Federico II, Via Cinthia 4, 80136 Napoli, Italy.
  • Nittoli V; Section of Pharmacognosy and Chemistry of Natural Products, Department of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopolis Zografou, Athens 15771, Greece.
  • Ambrosino C; Biogem, Istituto di Biologia e Genetica Molecolare, Via Camporeale, 83031 Ariano Irpino, Avellino, Italy.
  • Sordino P; Biogem, Istituto di Biologia e Genetica Molecolare, Via Camporeale, 83031 Ariano Irpino, Avellino, Italy.
  • Soluri A; Department of Science and Technology, University of Sannio, 82100 Benevento, Italy.
  • Soluri A; IEOS-CNR, 80131 Naples, Italy.
  • Massari R; Department of Biology and Evolution of Marine Organisms, Sicily Marine Centre, Stazione Zoologica Anton Dohrn, via Consolare Pompea 29, 98167 Messina,Italy.
  • D'Amelio M; National Research Council of Italy (CNR), c/o International Campus "A. Buzzati-Traverso″, Institute of Biochemistry and Cell Biology (IBBC), Via E. Ramarini, 32, Monterotondo Scalo, 00015 Rome, Italy.
  • De Palma R; National Research Council of Italy (CNR), c/o International Campus "A. Buzzati-Traverso″, Institute of Biochemistry and Cell Biology (IBBC), Via E. Ramarini, 32, Monterotondo Scalo, 00015 Rome, Italy.
  • Fontana A; Department of Medicine and Surgery, Unit of Molecular Neurosciences, University Campus Bio-Medico, via Álvaro del Portillo 21, 00128 Rome, Italy.
  • Manzo E; National Research Council of Italy (CNR), c/o International Campus "A. Buzzati-Traverso″, Institute of Biochemistry and Cell Biology (IBBC), Via E. Ramarini, 32, Monterotondo Scalo, 00015 Rome, Italy.
Anal Chem ; 96(8): 3362-3372, 2024 02 27.
Article em En | MEDLINE | ID: mdl-38348659
ABSTRACT
Recently, we described synthetic sulfolipids named Sulfavants as a novel class of molecular adjuvants based on the sulfoquinovosyl-diacylglycerol skeleton. The members of this family, Sulfavant A (1), Sulfavant R (2), and Sulfavant S (3), showed important effects on triggering receptor expressed on myeloid cells 2 (TREM2)-induced differentiation and maturation of human dendritic cells (hDC), through a novel cell mechanism underlying the regulation of the immune response. As these molecules are involved in biological TREM2-mediated processes crucial for cell survival, here, we report the synthesis and application of a fluorescent analogue of Sulfavant A bearing the 4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene moiety (Me4-BODIPY). The fluorescent derivative, named PB-SULF A (4), preserving the biological activity of Sulfavants, opens the way to chemical biology and cell biology experiments to better understand the interactions with cellular and in vivo organ targets and to improve our comprehension of complex molecular mechanisms underlying the not fully understood ligand-induced TREM2 activity.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Boro / Corantes Fluorescentes Limite: Humans Idioma: En Revista: Anal Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Boro / Corantes Fluorescentes Limite: Humans Idioma: En Revista: Anal Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália