TY - JOUR
T1 - Cell-derived vesicles for single-molecule imaging of membrane proteins
AU - Moonschi, Faruk H.
AU - Effinger, Amy K.
AU - Zhang, Xiaolu
AU - Martin, William E.
AU - Fox, Ashley M.
AU - Heidary, David K.
AU - DeRouchey, Jason E.
AU - Richards, Christopher I.
N1 - Publisher Copyright:
© 2015 Wiley-VCH Verlag GmbH & Co. KGaA.
PY - 2015/1/7
Y1 - 2015/1/7
N2 - A new approach is presented for the application of single-molecule imaging to membrane receptors through the use of vesicles derived from cells expressing fluorescently labeled receptors. During the isolation of vesicles, receptors remain embedded in the membrane of the resultant vesicles, thus allowing these vesicles to serve as nanocontainers for single-molecule measurements. Cell-derived vesicles maintain the structural integrity of transmembrane receptors by keeping them in their physiological membrane. It was demonstrated that receptors isolated in these vesicles can be studied with solution-based fluorescence correlation spectroscopy (FCS) and can be isolated on a solid substrate for single-molecule studies. This technique was applied to determine the stoichiometry of α3β4 nicotinic receptors. The method provides the capability to extend single-molecule studies to previously inaccessible classes of receptors.
AB - A new approach is presented for the application of single-molecule imaging to membrane receptors through the use of vesicles derived from cells expressing fluorescently labeled receptors. During the isolation of vesicles, receptors remain embedded in the membrane of the resultant vesicles, thus allowing these vesicles to serve as nanocontainers for single-molecule measurements. Cell-derived vesicles maintain the structural integrity of transmembrane receptors by keeping them in their physiological membrane. It was demonstrated that receptors isolated in these vesicles can be studied with solution-based fluorescence correlation spectroscopy (FCS) and can be isolated on a solid substrate for single-molecule studies. This technique was applied to determine the stoichiometry of α3β4 nicotinic receptors. The method provides the capability to extend single-molecule studies to previously inaccessible classes of receptors.
KW - Fluorescence correlation spectroscopy
KW - Fluorescence microscopy
KW - Single-molecule studies
KW - Transmembrane proteins
KW - Vesicles
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U2 - 10.1002/anie.201408707
DO - 10.1002/anie.201408707
M3 - Article
C2 - 25363667
AN - SCOPUS:84922730819
SN - 1433-7851
VL - 54
SP - 481
EP - 484
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 2
ER -