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Picomolar fluorescent probes for compound affinity determination to carbonic anhydrase IX expressed in live cancer cells.
Matuliene, Jurgita; Zvinys, Gediminas; Petrauskas, Vytautas; Kvietkauskaite, Agne; Zaksauskas, Audrius; Shubin, Kirill; Zubriene, Asta; Baranauskiene, Lina; Kacenauskaite, Lina; Kopanchuk, Sergei; Veiksina, Santa; Paketuryte-Latve, Vaida; Smirnoviene, Joana; Juozapaitiene, Vaida; Mickeviciute, Aurelija; Michailoviene, Vilma; Jachno, Jelena; Stravinskiene, Dovile; Sliziene, Aiste; Petrosiute, Agne; Becker, Holger M; Kazokaite-Adomaitiene, Justina; Yaromina, Ala; Capkauskaite, Edita; Rinken, Ago; Dudutiene, Virginija; Dubois, Ludwig J; Matulis, Daumantas.
Afiliação
  • Matuliene J; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Zvinys G; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Petrauskas V; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Kvietkauskaite A; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Zaksauskas A; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Shubin K; Latvian Institute of Organic Synthesis, Aizkraukles 21, Riga, LV-1006, Latvia.
  • Zubriene A; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Baranauskiene L; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Kacenauskaite L; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Kopanchuk S; Institute of Chemistry, University of Tartu, Ravila 14a, 50411, Tartu, Estonia.
  • Veiksina S; Institute of Chemistry, University of Tartu, Ravila 14a, 50411, Tartu, Estonia.
  • Paketuryte-Latve V; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Smirnoviene J; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Juozapaitiene V; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Mickeviciute A; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Michailoviene V; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Jachno J; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Stravinskiene D; Department of Immunology and Cell Biology, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Sliziene A; Department of Immunology and Cell Biology, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Petrosiute A; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Becker HM; Zoology and Animal Physiology, Institute of Zoology, TU Dresden, 01217, Dresden, Germany.
  • Kazokaite-Adomaitiene J; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Yaromina A; Division of Biochemistry, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Capkauskaite E; The M-Lab, Department of Precision Medicine, GROW - School for Oncology and Reproduction, Maastricht University, Universiteitssingel 50/23, 6200 MD, Maastricht, The Netherlands.
  • Rinken A; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Dudutiene V; Institute of Chemistry, University of Tartu, Ravila 14a, 50411, Tartu, Estonia.
  • Dubois LJ; Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio 7, LT-10257, Vilnius, Lithuania.
  • Matulis D; The M-Lab, Department of Precision Medicine, GROW - School for Oncology and Reproduction, Maastricht University, Universiteitssingel 50/23, 6200 MD, Maastricht, The Netherlands.
Sci Rep ; 12(1): 17644, 2022 10 21.
Article em En | MEDLINE | ID: mdl-36271018
Numerous human cancers, especially hypoxic solid tumors, express carbonic anhydrase IX (CAIX), a transmembrane protein with its catalytic domain located in the extracellular space. CAIX acidifies the tumor microenvironment, promotes metastases and invasiveness, and is therefore considered a promising anticancer target. We have designed a series of high affinity and high selectivity fluorescein-labeled compounds targeting CAIX to visualize and quantify CAIX expression in cancer cells. The competitive binding model enabled the determination of common CA inhibitors' dissociation constants for CAIX expressed in exponentially growing cancer cells. All tested sulfonamide compounds bound the proliferating cells with similar affinity as to recombinantly purified CAIX. The probes are applicable for the design of selective drug-like compounds for CAIX and the competition strategy could be applied to other drug targets.
Assuntos

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Anidrases Carbônicas / Neoplasias Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Lituânia

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Anidrases Carbônicas / Neoplasias Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Lituânia