Purification of Functional Human TRP Channels Recombinantly Produced in Yeast
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Purification of Functional Human TRP Channels Recombinantly Produced in Yeast. / Zhang, Liying; Wang, Kaituo; Klaerke, Dan Arne; Calloe, Kirstine; Lowrey, Lillian; Pedersen, Per Amstrup; Gourdon, Pontus; Gotfryd, Kamil.
In: Cells, Vol. 8, No. 2, 148, 2019, p. 1-20.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Purification of Functional Human TRP Channels Recombinantly Produced in Yeast
AU - Zhang, Liying
AU - Wang, Kaituo
AU - Klaerke, Dan Arne
AU - Calloe, Kirstine
AU - Lowrey, Lillian
AU - Pedersen, Per Amstrup
AU - Gourdon, Pontus
AU - Gotfryd, Kamil
PY - 2019
Y1 - 2019
N2 - (1) Background: Human transient receptor potential (TRP) channels constitute a large family of ion-conducting membrane proteins that allow the sensation of environmental cues. As the dysfunction of TRP channels contributes to the pathogenesis of many widespread diseases, including cardiac disorders, these proteins also represent important pharmacological targets. TRP channels are typically produced using expensive and laborious mammalian or insect cell-based systems. (2) Methods: We demonstrate an alternative platform exploiting the yeast Saccharomyces cerevisiae capable of delivering high yields of functional human TRP channels. We produce 11 full-length human TRP members originating from four different subfamilies, purify a selected subset of these to a high homogeneity and confirm retained functionality using TRPM8 as a model target. (3) Results: Our findings demonstrate the potential of the described production system for future functional, structural and pharmacological studies of human TRP channels.
AB - (1) Background: Human transient receptor potential (TRP) channels constitute a large family of ion-conducting membrane proteins that allow the sensation of environmental cues. As the dysfunction of TRP channels contributes to the pathogenesis of many widespread diseases, including cardiac disorders, these proteins also represent important pharmacological targets. TRP channels are typically produced using expensive and laborious mammalian or insect cell-based systems. (2) Methods: We demonstrate an alternative platform exploiting the yeast Saccharomyces cerevisiae capable of delivering high yields of functional human TRP channels. We produce 11 full-length human TRP members originating from four different subfamilies, purify a selected subset of these to a high homogeneity and confirm retained functionality using TRPM8 as a model target. (3) Results: Our findings demonstrate the potential of the described production system for future functional, structural and pharmacological studies of human TRP channels.
U2 - 10.3390/cells8020148
DO - 10.3390/cells8020148
M3 - Journal article
C2 - 30754715
VL - 8
SP - 1
EP - 20
JO - Cells
JF - Cells
SN - 2073-4409
IS - 2
M1 - 148
ER -
ID: 213713237