Practical and reliable FRET/FLIM pair of fluorescent proteins

Dmitry Shcherbo, Ekaterina A. Souslova, Joachim Goedhart, Tatyana V. Chepurnykh, Anna Gaintzeva, Irina I. Shemiakina, Theodorus W.J. Gadella, Sergey Lukyanov, Dmitriy M. Chudakov

Результат исследований: Вклад в журналСтатьярецензирование

80 Цитирования (Scopus)


Background: In spite of a great number of monomeric fluorescent proteins developed in the recent years, the reported fluorescent protein-based FRET pairs are still characterized by a number of disadvantageous features, complicating their use as reporters in cell biology and for high-throughput cell-based screenings. Results: Here we screened some of the recently developed monomeric protein pairs to find the optimal combination, which would provide high dynamic range FRET changes, along with high pH- and photo-stability, fast maturation and bright fluorescence, and reliable detection in any fluorescent imaging system. Among generated FRET pairs, we have selected TagGFP-TagRFP, combining all the mentioned desirable characteristics. On the basis of this highly efficient FRET pair, we have generated a bright, high contrast, pH- and photo-stable apoptosis reporter, named CaspeR3 (Caspase 3 Reporter). Conclusion: The combined advantages suggest that the TagGFP-TagRFP is one of the most efficient green/red couples available to date for FRET/ FLIM analyses to monitor interaction of proteins of interest in living cells and to generate FRET-based sensors for various applications. CaspeR3 provides reliable detection of apoptosis, and should become a popular tool both for cell biology studies and high throughput screening assays.

Язык оригиналаАнглийский
Номер статьи24
ЖурналBMC Biotechnology
СостояниеОпубликовано - 25 мар. 2009
Опубликовано для внешнего пользованияДа


Подробные сведения о темах исследования «Practical and reliable FRET/FLIM pair of fluorescent proteins». Вместе они формируют уникальный семантический отпечаток (fingerprint).