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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.


Top mentioned proteins: PLC, CAN, Rhodopsin, ACID, V1a
Papers on TRPL
CULD is required for rhodopsin and TRPL channel endocytic trafficking and survival of photoreceptor cells.
Wang et al., Beijing, China. In J Cell Sci, Feb 2016
In Drosophila melanogaster, the main light-sensing rhodopsin (Rh1; encoded by ninaE) and the downstream ion channel, transient receptor potential like (TRPL), are endocytosed in response to light, but the mechanism is unclear.
Phototransduction in Drosophila.
Juusola et al., Cambridge, United Kingdom. In Curr Opin Neurobiol, Oct 2015
Phototransduction in Drosophila's microvillar photoreceptors is mediated by phospholipase C (PLC) resulting in activation of two distinct Ca(2+)-permeable channels, TRP and TRPL.
The GTP- and Phospholipid-Binding Protein TTD14 Regulates Trafficking of the TRPL Ion Channel in Drosophila Photoreceptor Cells.
Huber et al., Stuttgart, Germany. In Plos Genet, Oct 2015
In photoreceptors of Drosophila, light absorption by rhodopsin triggers a phospholipase Cβ-mediated opening of the ion channels transient receptor potential (TRP) and TRP-like (TRPL) and generates the visual response.
Speed and sensitivity of phototransduction in Drosophila depend on degree of saturation of membrane phospholipids.
Hardie et al., Cambridge, United Kingdom. In J Neurosci, Mar 2015
Recent evidence, including the demonstration that light evokes rapid contractions of the photoreceptors, suggested that the light-sensitive channels (TRP and TRPL) may be mechanically gated, together with protons released by PLC-mediated PIP2 hydrolysis.
Observation of multiple, identical binding sites in the exchange of carboxylic acid ligands with CdS nanocrystals.
Tang et al., Riverside, United States. In Nano Lett, 2014
Assuming Poissonian binding statistics, our model fits both steady-state and time-resolved photoluminescence (SSPL and TRPL, respectively) data well.
Effects of cyclodextrins on intramolecular photoinduced electron transfer in a boronic acid fluorophore.
Ema et al., In Anal Sci, 2013
We have investigated the PET process in C1-APB/CyD complexes by using time-resolved photoluminescence (TRPL) measurements at room temperature, and have succeeded in estimating the electron-transfer time to be about 1 ns.
Photosensitive TRPs.
Hardie, Cambridge, United Kingdom. In Handb Exp Pharmacol, 2013
Together with a second TRPC channel, trp-like (TRPL), TRP mediates the transducer current in the fly's photoreceptors.
Photomechanical responses in Drosophila photoreceptors.
Franze et al., Cambridge, United Kingdom. In Science, 2012
PLC hydrolyzes the minor membrane lipid phosphatidylinositol 4,5-bisphosphate (PIP(2)), leading by an unknown mechanism to activation of the prototypical transient receptor potential (TRP) and TRP-like (TRPL) channels.
The regulations of Drosophila phototransduction.
Kim et al., United States. In J Neurogenet, 2012
The report includes our studies on the regulations and/or the functions of arrestin II (Arr2), norpA (PLC), inactivation no afterpotential D (INAD), transient receptor potential (TRP), TRP-like (TRPL), inactivation no afterpotential E (INAE), and Porin.
The activity of the TRP-like channel depends on its expression system.
Minke et al., Jerusalem, Israel. In Channels (austin), 2012
TRPL channel is constitutively active in S2 cells but is silent in HEK cells.
Signal-dependent hydrolysis of phosphatidylinositol 4,5-bisphosphate without activation of phospholipase C: implications on gating of Drosophila TRPL (transient receptor potential-like) channel.
Minke et al., Jerusalem, Israel. In J Biol Chem, 2012
PI(4,5)P(2) is a crucial substrate for PLC-mediated activation of the trpl channels, whereas PUFA may function as the channel activator.
Phototransduction in Drosophila.
Han et al., Nanjing, China. In Sci China Life Sci, 2012
Based on the functional characterization of these genes, a model for Drosophila phototransduction has been outlined, including rhodopsin activation, phosphoinoside signaling, and the opening of TRP and TRPL channels.
Mechanisms underlying stage-1 TRPL channel translocation in Drosophila photoreceptors.
Tsunoda et al., Boston, United States. In Plos One, 2011
The involvement of de novo protein synthesis in TRPL translocation, was examined.
Translocation of the Drosophila transient receptor potential-like (TRPL) channel requires both the N- and C-terminal regions together with sustained Ca2+ entry.
Huber et al., Stuttgart, Germany. In J Biol Chem, 2011
the essential function of the TRP channels in TRPL translocation is to enhance Ca(2+)-influx.
The Drosophila TRPL ion channel shares a Rab-dependent translocation pathway with rhodopsin.
Huber et al., Stuttgart, Germany. In Eur J Cell Biol, 2011
found that rab proteins, Rab5 and RabX4, are required for the internalization of TRPL into the cell body
Gating mechanisms of canonical transient receptor potential channel proteins: role of phosphoinositols and diacylglycerol.
Albert, London, United Kingdom. In Adv Exp Med Biol, 2010
Canonical transient receptor potential (TRPC) Ca(2+)-permeable channels are members of the mammalian TRP super-family of cation channels, and have the closest homology to the founding members, TRP and TRPL, discovered in Drosophila photoreceptors.
Illumination of the melanopsin signaling pathway.
Jegla et al., San Diego, United States. In Science, 2005
We also found that melanopsin could activate the cation channel TRPC3, a mammalian homolog of the Drosophila phototransduction channels TRP and TRPL.
Polyunsaturated fatty acids activate the Drosophila light-sensitive channels TRP and TRPL.
Hardie et al., Cambridge, United Kingdom. In Nature, 1999
Here we show that both of these fatty acids reversibly activate native light-sensitive channels (transient receptor potential (TRP) and TRP-like (TRPL)) in Drosophila photoreceptors as well as recombinant TRPL channels expressed in Drosophila S2 cells.
Calmodulin regulation of Drosophila light-activated channels and receptor function mediates termination of the light response in vivo.
Zuker et al., San Diego, United States. In Cell, 1997
Contrary to current models of excitation and TRP channel function, we demonstrate that the transient phenotype of trp mutants can be explained by CAM regulation of the TRPL channel rather than by the loss of a store-operated conductance leading to depletion of the internal stores.
Coassembly of TRP and TRPL produces a distinct store-operated conductance.
Montell et al., Baltimore, United States. In Cell, 1997
In vitro studies indicate that TRP is a SOC, but that the related retinal protein, TRPL, is constitutively active.
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