Rational design of chemical ligands for selective mitochondrial targeting
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23961900
DOI
10.1021/bc400291f
Knihovny.cz E-zdroje
- MeSH
- buněčné linie MeSH
- DNA analýza MeSH
- fluorescenční barviva analýza metabolismus MeSH
- kardiolipiny analýza metabolismus MeSH
- krystalografie rentgenová MeSH
- kultivované buňky MeSH
- kur domácí MeSH
- lidé MeSH
- ligandy MeSH
- mitochondrie metabolismus ultrastruktura MeSH
- molekulární modely MeSH
- myši MeSH
- nádorové buněčné linie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA MeSH
- fluorescenční barviva MeSH
- kardiolipiny MeSH
- ligandy MeSH
The rational design of molecules with selective intracellular targeting is a great challenge for contemporary chemistry and life sciences. Here, we demonstrate a rational approach to development of compartment-specific fluorescent dyes from the γ-aryl substituted pentamethine family. These novel dyes exhibit an extraordinary affinity and selectivity for cardiolipin in inner mitochondrial membrane and possess excellent photostability, fluorescent properties, and low phototoxicity. Selective imaging of live and fixed mitochondria was achieved in various cell lines using nanomolar concentrations of these dyes. Their high localization specificity and low toxicity enables study of morphological changes, structural complexity, and dynamics of mitochondria playing a pivotal role in many pathological diseases. These far-red emitting dyes could also serve in a variety of biomedical applications.
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