Real-time measurement of endosomal acidification by a novel genetically encoded biosensor

被引:36
作者
Serresi, Michela [1 ,2 ]
Bizzarri, Ranieri [1 ,2 ,3 ]
Cardarelli, Francesco [1 ,2 ,3 ]
Beltram, Fabio [1 ,2 ,3 ]
机构
[1] Scuola Normale Super Pisa, NEST, I-56124 Pisa, Italy
[2] Italian Inst Technol, I-56124 Pisa, Italy
[3] CNR INFM, I-56124 Pisa, Italy
关键词
Biosensor; Endocytosis; GFP; In vivo imaging; pH measurement; Tat-HIV protein; GREEN FLUORESCENT PROTEIN; EMISSION PH SENSORS; ARGININE-RICH MOTIF; ENDOCYTOSIS; LYSOSOMES; PATHWAY; LIGAND; CELLS; MITOCHONDRIAL; DEGRADATION;
D O I
10.1007/s00216-008-2489-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Genetically encoded fluorescent proteins are optimal reporters when used to monitor cellular processes as they can be targeted to any subcellular region by fusion to a protein of interest. Here, we present the pH-sensitive fluorescent protein E(1)GFP which is ideally suited to monitor pH changes in dynamic intracellular structures in real time with high spatio temporal resolution. E(1)GFP is a ratiometric pH indicator by emission with a pK close to 6.0. We describe an application of this novel pH reporter in the measurement of pH changes along the endo-lysosomal pathway. By fusing E(1)GFP to the HIV-Tat protein which is endowed with cell-penetrating properties, we were able to monitor multi-step endocytosis from the initial cell-surface binding through to the intracellular endocytic network in real time. This represents a framework for the application of E(1)GFP to the in situ detection of pH changes involved in dynamic biological phenomena.
引用
收藏
页码:1123 / 1133
页数:11
相关论文
共 34 条
[1]   Mitochondrial pH monitored by a new engineered green fluorescent protein mutant [J].
Abad, MFC ;
Di Benedetto, G ;
Magalhaes, PJ ;
Filippin, L ;
Pozzan, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (12) :11521-11529
[2]   Spectroscopic and structural study of proton and halide ion cooperative binding to GFP [J].
Arosio, Daniele ;
Garau, Gianpiero ;
Ricci, Fernanda ;
Marchetti, Laura ;
Bizzarri, Ranieri ;
Nifosi, Riccardo ;
Beltram, Fabio .
BIOPHYSICAL JOURNAL, 2007, 93 (01) :232-244
[3]   The ESCRT-III subunit hVps24 is required for degradation but not silencing of the epidermal growth factor receptor [J].
Bache, Kristi G. ;
Stuffers, Susanne ;
Malerod, Lene ;
Slagsvold, Thomas ;
Raiborg, Camilla ;
Lechardeur, Delphine ;
Walchli, Sebastien ;
Lukacs, Gergely L. ;
Brech, Andreas ;
Stenmark, Harald .
MOLECULAR BIOLOGY OF THE CELL, 2006, 17 (06) :2513-2523
[4]   Development of a novel GFP-based ratiometric excitation and emission pH indicator for intracellular studies [J].
Bizzarri, R ;
Arcangeli, C ;
Arosio, D ;
Ricci, F ;
Faraci, P ;
Cardarelli, F ;
Beltram, F .
BIOPHYSICAL JOURNAL, 2006, 90 (09) :3300-3314
[5]   Green fluorescent protein ground states: The influence of a second protonation site near the chromophore [J].
Bizzarri, Ranieri ;
Nifosi, Riccardo ;
Abbruzzetti, Stefania ;
Rocchia, Walter ;
Guidi, Sara ;
Arosio, Daniele ;
Garau, Gianpiero ;
Campanini, Barbara ;
Grandi, Elena ;
Ricci, Fernanda ;
Viappiani, Cristiano ;
Beltram, Fabio .
BIOCHEMISTRY, 2007, 46 (18) :5494-5504
[6]   Endocytic delivery to lysosomes mediated by concurrent fusion and kissing events in living cells [J].
Bright, NA ;
Gratian, MJ ;
Luzio, JP .
CURRENT BIOLOGY, 2005, 15 (04) :360-365
[7]   Tuning the transport properties of HIV-1 tat arginine-rich motif in living cells [J].
Cardarelli, Francesco ;
Serresi, Michela ;
Bizzarri, Ranieri ;
Beltram, Fabio .
TRAFFIC, 2008, 9 (04) :528-539
[8]   In vivo study of HIV-1 Tat arginine-rich motif unveils its transport properties [J].
Cardarelli, Francesco ;
Serresi, Michela ;
Bizzarri, Ranieri ;
Giacca, Mauro ;
Beltram, Fabio .
MOLECULAR THERAPY, 2007, 15 (07) :1313-1322
[9]   Ligand binding induces Cbl-dependent EphB1 receptor degradation through the lysosomal pathway [J].
Fasen, Katrin ;
Cerretti, Douglas Pat ;
Huynh-Do, Uyen .
TRAFFIC, 2008, 9 (02) :251-266
[10]   CELLULAR UPTAKE OF THE TAT PROTEIN FROM HUMAN IMMUNODEFICIENCY VIRUS [J].
FRANKEL, AD ;
PABO, CO .
CELL, 1988, 55 (06) :1189-1193