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1 NCS-1 and PI4Kbeta coimmunoprecipitate, opening up the p
2 NCS-1 and TRPC5 are in the same protein complex in rat b
3 NCS-1 binds directly to PICK1 via its BAR domain in a Ca
4 NCS-1 is a multispecific protein interacting with a numb
5 NCS-1 was shown to modulate the effects of expression of
6 NCS-1-D2 receptor interaction may serve to couple dopami
7 that the neuronal calcium sensor protein-1 (NCS-1), another member of the recoverin-neuronal calcium
8 n, which degrades neuronal calcium sensor 1 (NCS-1) and subsequent loss of intracellular calcium sign
9 the Ca(2+) sensor neuronal calcium sensor 1 (NCS-1) and the guanine exchange factor protein Ric8a cor
12 ific reduction in neuronal calcium sensor 1 (NCS-1) protein levels, a known modulator of InsP(3) rece
13 l binding protein, neuronal Ca(2+) sensor 1 (NCS-1), a Ca(2+) binding protein that interacts with the
15 tween paclitaxel, neuronal calcium sensor 1 (NCS-1), and the inositol 1,4,5-trisphosphate receptor (I
16 ess I(Ca), unless neuronal calcium sensor-1 (NCS-1) activity was blocked by a dominant-negative NCS-1
19 ts mammalian homolog neuronal Ca2+ sensor-1 (NCS-1) belong to a family of Ca2+ sensors with EF hands
20 we show that the neuronal calcium sensor-1 (NCS-1) can mediate desensitization of D2 dopamine recept
21 m binding protein neuronal calcium sensor-1 (NCS-1) can switch paired-pulse depression to facilitatio
22 eins (KChIPs) and neuronal calcium sensor-1 (NCS-1) have been shown to interact with Kv4 channel alph
29 tudy, addition of neuronal calcium sensor-1 (NCS-1), a high-affinity, low-capacity, calcium-binding p
30 with that of the neuronal calcium sensor-1 (NCS-1), a neuron-specific calcium-binding and D2-interac
31 -binding protein, neuronal calcium sensor-1 (NCS-1), can physically associate with the type III PI4Kb
32 in, also known as neuronal calcium sensor-1 (NCS-1), is an N-myristoylated Ca2+-binding protein that
33 mination of the crystal structures of Ca(2+)/NCS-1 alone and in complex with peptides derived from D2
36 hat this adaptive signalling network (Cav1.3/NCS-1/D2/GIRK2) is also active in human SN DA neurons, a
42 is with chimeric proteins between KChIP2 and NCS-1 reveals that the three regions of KChIP2 (the link
43 ce in these three regions between KChIPs and NCS-1 determines the specificity and affinity for intera
44 When expressed in COS-7 cells, PI4Kbeta and NCS-1 formed a complex that could be immunoprecipitated
49 suggest protein-protein interaction between NCS-1 and TRPC5, and involvement of this protein complex
51 and D2-autoreceptor activity, controlled by NCS-1, and indicate that this adaptive signalling networ
52 the different molecular states populated by NCS-1 was monitored in real time through constant-force
59 av2.3 deficiency upregulated transcripts for NCS-1, a Ca(2+)-binding protein implicated in neuroprote
62 to NCS-1 shifted titration curves to higher NCS-1 concentrations, suggesting that the binding of NCS
63 When cells were stimulated with histamine, NCS-1 overexpression led to higher exocytosis, as well a
65 ing proteins on Kv4 channel gating, however, NCS-1 co-expression does not measurably affect the volta
69 and Ca(2+)-induced conformational changes in NCS-1 as compared with the role in the nonmyristoylated
71 lished after a single amino acid mutation in NCS-1 that has been shown to impair the calcium-binding
72 activation of calpain and the reductions in NCS-1 levels and calcium signaling associated with these
73 interface and uncovers a suitable region in NCS-1 for development of additional drugs of potential u
74 to study the folding behavior of individual NCS-1 molecules in the presence of Mg(2+) and in the abs
75 on InsP3R1 function, suggesting that InsP3R1/NCS-1 interaction is an essential component of the patho
79 her observed that short hairpin RNA-mediated NCS-1 knockdown had a similar effect on phosphoinositide
84 ee of cooperativity; thus, the myristoylated NCS-1 binds Ca(2+) more strongly (with three Ca(2+) bind
86 nt protein imaging show that KChIPs (but not NCS-1) effectively bind to Kv4.3 protein and localize at
92 ncentrations, suggesting that the binding of NCS-1 to the D2R is highly specific and that binding occ
99 u-calpain, which leads to the degradation of NCS-1, which, in turn, attenuates InsP(3)mediated Ca(2+)
100 tochemistry showed a similar distribution of NCS-1 and phosphatidylinositol 4-kinase beta (PI4Kbeta).
102 Lithium inhibited the enhancing effect of NCS-1 on InsP3R1 function, suggesting that InsP3R1/NCS-1
110 In intact cells, enhanced expression of NCS-1 resulted in increased intracellular calcium releas
111 We propose, therefore, that the function of NCS-1 in mammals may closely resemble that of Frq1 in S.
112 Short hairpin RNA-mediated knockdown of NCS-1 in the same cell line abrogated the response to ta
113 antia nigra dopamine messenger RNA levels of NCS-1 (but not Cav1.2 or Cav1.3) after cocaine in mice,
117 fluorescence anisotropy (FA) and a panel of NCS-1 EF-hand variants to interrogate the interaction be
118 sults allowed us to trace the progression of NCS-1 folding along its energy landscapes and provided a
121 ta suggest multiple and overlapping roles of NCS-1 in the developing and mature olfactory system.
122 P2 position of the calpain cleavage site of NCS-1 to decrease the likelihood of NCS-1 degradation.
123 made possible by the C-lobe-binding site of NCS-1, which adopts alternative conformations in each co
124 Under tension, the Mg(2+)-bound state of NCS-1 unfolds and refolds in a three-state process by po
126 Expression of either mutated version of NCS-1 in neuroblastoma cells protected intracellular cal
128 green fluorescent protein (GFP) or GFP plus NCS-1, except that the overexpression of NCS-1 resulted
137 studies revealed that these compounds target NCS-1, overlap the D(2)R binding site, and perturb the d
138 expressed in adult mouse ventricles and that NCS-1 co-immunoprecipitates with Kv4.3 from (adult mouse
139 pitation experiments in HEK-293 confirm that NCS-1 can oligomerize in cell lysates and that oligomeri
141 in vitro and cellular assays, we found that NCS-1 promotes D(2)R trafficking to the plasma membrane
143 an embryonic kidney 293 cells indicates that NCS-1 attenuates agonist-induced receptor internalizatio
145 ression studies in HEK-293 cells reveal that NCS-1 increases membrane expression of Kv4 alpha-subunit
146 xperiments from striatal neurons reveal that NCS-1 is found in association with both the D2 receptor
147 g(2+) FA titration experiments revealed that NCS-1 EF-hands 2-4 (EF2-4) contributed to binding with t
150 Taken together, these results suggest that NCS-1 is an accessory subunit of Kv4-encoded I(to,f) cha
154 ystallographic data reported here define the NCS-1/Ric-8A interface and will allow the development of
162 d the large hydrophobic crevice based on the NCS-1 crystal structure, this crevice may be the associa
165 ant that formed a dimer, indicating that the NCS-1 C-terminal region prevents NCS-1 oligomerization.
167 compete with labeled peptide for binding to NCS-1 shifted titration curves to higher NCS-1 concentra
169 y a model in which the D2R peptide binds two NCS-1 monomers sequentially in a cooperative fashion.
171 However, the molecular mechanism by which NCS-1 regulates Ric-8A activity and its interaction with
172 nt in bipolar disorders, conditions in which NCS-1 is highly expressed, we tested the effect of lithi
173 aved more favorably by calpain compared with NCS-1 WT, whereas the other mutant was less favorably cl
174 ) activity toward Galpha when complexed with NCS-1, and restoration of nucleotide exchange activity u
177 findings suggest that ARF-1.1 interacts with NCS-1 in AIY neurons and potentially pifk-1 in the Ca(2+
178 The aminophenothiazine FD44 interferes with NCS-1/Ric8a binding, and it restores normal synapse numb