TY - JOUR
T1 - A novel cell-based scintillation proximity assay for studying protein function and activity in vitro using membrane-soluble scintillants
AU - Culliford, Steven J.
AU - McCauley, Patrick
AU - Sutherland, Andrew J.
AU - McCairn, Mark
AU - Sutherland, John
AU - Blackburn, Jonathan
AU - Kozlowski, Roland Z.
PY - 2002/8/30
Y1 - 2002/8/30
N2 - Here we describe for the first time a cell-based scintillation proximity assay using membrane soluble scintillants (MSS). MSS have a scintillant 'head' group (2,5-diphenyloxazole) attached to a lipophilic 'tail.' MSS do not scintillate in an aqueous environment in the presence of a radioactive source: however, in a non-aqueous environment, such as a lipid bilayer (e.g., liposome or cell membrane), scintillation does occur. MSS can be incorporated into liposomes. When these MSS-containing liposomes are fused with the plasma membranes of cells in culture the MSS are incorporated into the cell membrane. Radiolabelled molecules in close proximity to the cell membrane will then elicit a scintillation signal. This system has been used to successfully monitor [14C]methionine uptake in HeLa cells and may be used in radiochemical and radioligand binding assays either in vivo or on microsomal preparations obtained from tissues. This new scintillation proximity technology could be readily adapted for high-throughput screening.
AB - Here we describe for the first time a cell-based scintillation proximity assay using membrane soluble scintillants (MSS). MSS have a scintillant 'head' group (2,5-diphenyloxazole) attached to a lipophilic 'tail.' MSS do not scintillate in an aqueous environment in the presence of a radioactive source: however, in a non-aqueous environment, such as a lipid bilayer (e.g., liposome or cell membrane), scintillation does occur. MSS can be incorporated into liposomes. When these MSS-containing liposomes are fused with the plasma membranes of cells in culture the MSS are incorporated into the cell membrane. Radiolabelled molecules in close proximity to the cell membrane will then elicit a scintillation signal. This system has been used to successfully monitor [14C]methionine uptake in HeLa cells and may be used in radiochemical and radioligand binding assays either in vivo or on microsomal preparations obtained from tissues. This new scintillation proximity technology could be readily adapted for high-throughput screening.
KW - Cell membrane
KW - Intact cells
KW - Radioisotope assays
KW - Scintillation proximity
KW - SPA
UR - http://www.scopus.com/inward/record.url?scp=0036386377&partnerID=8YFLogxK
UR - https://www.sciencedirect.com/science/article/abs/pii/S0006291X02009440?via%3Dihub
U2 - 10.1016/S0006-291X(02)00944-0
DO - 10.1016/S0006-291X(02)00944-0
M3 - Article
C2 - 12200126
AN - SCOPUS:0036386377
SN - 0006-291X
VL - 296
SP - 857
EP - 863
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -