Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Hinako Suga"'
Publikováno v:
学苑 = Gakuen. 962:8-15
G protein-coupled receptors are cell-surface receptors, many of which have conserved motif F(x)6LL in their C-terminal intracellular region. The motif is known to function when the G protein-coupled receptors are exported from the endoplasmic ret
Publikováno v:
British Journal of Pharmacology. 160:1534-1549
Background and purpose: We investigated how McN-A-343 inhibited the alkylation of the M1 muscarinic receptor by its nitrogen mustard derivative and that of ACh to identify whether it interacts allosterically or orthosterically. Experimental approach:
Autor:
Hinako Suga, Frederick J. Ehlert
Publikováno v:
Biochemical Pharmacology. 79:1025-1035
We investigated whether the aziridinium ion formed from a nitrogen mustard derivative (4-[(2-bromoethyl)methyl-amino]-2-butynyl N-(3-chlorophenyl)carbamate; BR384) structurally related to McN-A-343 (4-(trimethyl-amino)-2-butynyl N-(3-chlorophenyl)car
Autor:
Hinako Suga, Tatsuya Haga
Publikováno v:
Neurochemistry International. 51:140-164
G protein-coupled receptors (GPCRs) constitute one of the largest families of genes in the human genome, and are the largest targets for drug development. Although a large number of GPCR genes have recently been identified, ligands have not yet been
Autor:
Akiko, MORI, Naoko, YAMADA, Chikako, YOSHIDA, Kyoichi, TAKAO, Fumihiko, KOIKE, Hiromi, KAZAMA, Hinako, SUGA, Tetsuya, TAKAO
Publikováno v:
學苑 = GAKUEN. 782:57-63
RT-PCR法を用いて,葉状乳頭における味覚受容体の発現を検討した。すなわち葉状乳頭部から擦過法により取得した組織を使用し,味覚受容体候補であるTHTRファミリー(THTRs)およびT2Rファミリ
Publikováno v:
學苑 = GAKUEN. 770:95-100
Gタンパク質共役受容体THTR5をCHO細胞に導入し,呈味物質への応答性を検討した。THTR5クローンにおいてはGlucose, Fructose, Sorbitol, Arginine, Denatonium benzoate, Guanosin 5monophosphate disodium salt, Inosin 5'mono
Publikováno v:
Journal of Biochemistry. 135:605-613
We examined whether fusion proteins of G protein-coupled receptors with the alpha subunit of G(16) (Galpha(16)) could activate downstream signals. We expressed fusion proteins of G(i)-coupled receptors, i.e. CX(3)C chemokine receptor 1 (CX(3)CR1) and
Publikováno v:
學苑 = GAKUEN. 758:54-61
Autor:
Frederick J. Ehlert, Hinako Suga
Publikováno v:
Biochemistry. 52(29)
We investigated how asparagine mutagenesis of conserved aspartic acids in helix two (D2.50) and three (D3.32) of M1 – M4 muscarinic receptors alters the irreversible binding of acetylcholine mustard and BR384 (4-[(2-bromoethyl)methyl-amino]-2-butyn
Publikováno v:
Journal of visualized experiments : JoVE. (58)
When an agonist activates a population of G protein-coupled receptors (GPCRs), it elicits a signaling pathway that culminates in the response of the cell or tissue. This process can be analyzed at the level of a single receptor, a population of recep