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Quantitative assessment of fluorescent proteins.
Cranfill, Paula J; Sell, Brittney R; Baird, Michelle A; Allen, John R; Lavagnino, Zeno; de Gruiter, H Martijn; Kremers, Gert-Jan; Davidson, Michael W; Ustione, Alessandro; Piston, David W.
Afiliación
  • Cranfill PJ; National High Field Magnet Lab, Florida State University, Tallahassee, Florida, USA.
  • Sell BR; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, USA.
  • Baird MA; National High Field Magnet Lab, Florida State University, Tallahassee, Florida, USA.
  • Allen JR; National High Field Magnet Lab, Florida State University, Tallahassee, Florida, USA.
  • Lavagnino Z; National High Field Magnet Lab, Florida State University, Tallahassee, Florida, USA.
  • de Gruiter HM; Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee, USA.
  • Kremers GJ; Department of Cell Biology and Physiology, Washington University, St. Louis, Missouri, USA.
  • Davidson MW; Erasmus Optical Imaging Centre, Josephine Nefkens Institute, Erasmus MC, Rotterdam, the Netherlands.
  • Ustione A; Erasmus Optical Imaging Centre, Josephine Nefkens Institute, Erasmus MC, Rotterdam, the Netherlands.
  • Piston DW; National High Field Magnet Lab, Florida State University, Tallahassee, Florida, USA.
Nat Methods ; 13(7): 557-62, 2016 07.
Article en En | MEDLINE | ID: mdl-27240257
ABSTRACT
The advent of fluorescent proteins (FPs) for genetic labeling of molecules and cells has revolutionized fluorescence microscopy. Genetic manipulations have created a vast array of bright and stable FPs spanning blue to red spectral regions. Common to autofluorescent FPs is their tight ß-barrel structure, which provides the rigidity and chemical environment needed for effectual fluorescence. Despite the common structure, each FP has unique properties. Thus, there is no single 'best' FP for every circumstance, and each FP has advantages and disadvantages. To guide decisions about which FP is right for a given application, we have quantitatively characterized the brightness, photostability, pH stability and monomeric properties of more than 40 FPs to enable straightforward and direct comparison between them. We focus on popular and/or top-performing FPs in each spectral region.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espectrometría de Fluorescencia / Proteínas Recombinantes de Fusión / Proteínas Luminiscentes / Microscopía Fluorescente Límite: Humans Idioma: En Revista: Nat Methods Asunto de la revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espectrometría de Fluorescencia / Proteínas Recombinantes de Fusión / Proteínas Luminiscentes / Microscopía Fluorescente Límite: Humans Idioma: En Revista: Nat Methods Asunto de la revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos