Your browser doesn't support javascript.
loading
N-Cyanorhodamines: cell-permeant, photostable and bathochromically shifted analogues of fluoresceins.
Heynck, Lukas; Matthias, Jessica; Bossi, Mariano L; Butkevich, Alexey N; Hell, Stefan W.
Afiliação
  • Heynck L; Department of Optical Nanoscopy, Max Planck Institute for Medical Research 69120 Heidelberg Germany alexey.butkevich@mr.mpg.de.
  • Matthias J; Department of Optical Nanoscopy, Max Planck Institute for Medical Research 69120 Heidelberg Germany alexey.butkevich@mr.mpg.de.
  • Bossi ML; Department of NanoBiophotonics, Max Planck Institute for Multidisciplinary Sciences 37077 Göttingen Germany.
  • Butkevich AN; Department of Optical Nanoscopy, Max Planck Institute for Medical Research 69120 Heidelberg Germany alexey.butkevich@mr.mpg.de.
  • Hell SW; Department of NanoBiophotonics, Max Planck Institute for Multidisciplinary Sciences 37077 Göttingen Germany.
Chem Sci ; 13(28): 8297-8306, 2022 Jul 20.
Article em En | MEDLINE | ID: mdl-35919709
ABSTRACT
Fluorescein and its analogues have found only limited use in biological imaging because of the poor photostability and cell membrane impermeability of their O-unprotected forms. Herein, we report rationally designed N-cyanorhodamines as orange- to red-emitting, photostable and cell-permeant fluorescent labels negatively charged at physiological pH values and thus devoid of off-targeting artifacts often observed for cationic fluorophores. In combination with well-established fluorescent labels, self-labelling protein (HaloTag, SNAP-tag) ligands derived from N-cyanorhodamines permit up to four-colour confocal and super-resolution STED imaging in living cells.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Sci Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Sci Ano de publicação: 2022 Tipo de documento: Article