Presence of carbohydrate binding modules in extracellular region of class C G-protein coupled receptors (C GPCR): An in silico investigation on sweet taste receptor

2019 ◽  
Vol 44 (6) ◽  
Author(s):  
Elaheh Kashani-Amin ◽  
Amirhossein Sakhteman ◽  
Bagher Larijani ◽  
Azadeh Ebrahim-Habibi
2013 ◽  
Vol 27 (8) ◽  
pp. 1188-1197 ◽  
Author(s):  
Eric M. Wauson ◽  
Andrés Lorente-Rodríguez ◽  
Melanie H. Cobb

G protein-coupled receptors (GPCRs) are membrane proteins that recognize molecules in the extracellular milieu and transmit signals inside cells to regulate their behaviors. Ligands for many GPCRs are hormones or neurotransmitters that direct coordinated, stereotyped adaptive responses. Ligands for other GPCRs provide information to cells about the extracellular environment. Such information facilitates context-specific decision making that may be cell autonomous. Among ligands that are important for cellular decisions are amino acids, required for continued protein synthesis, as metabolic starting materials and energy sources. Amino acids are detected by a number of class C GPCRs. One cluster of amino acid-sensing class C GPCRs includes umami and sweet taste receptors, GPRC6A, and the calcium-sensing receptor. We have recently found that the umami taste receptor heterodimer T1R1/T1R3 is a sensor of amino acid availability that regulates the activity of the mammalian target of rapamycin. This review focuses on an array of findings on sensing amino acids and sweet molecules outside of neurons by this cluster of class C GPCRs and some of the physiologic processes regulated by them.


2019 ◽  
Vol 77 (3) ◽  
pp. 227-243 ◽  
Author(s):  
Elaheh Kashani-Amin ◽  
Amirhossein Sakhteman ◽  
Bagher Larijani ◽  
Azadeh Ebrahim-Habibi

ChemInform ◽  
2006 ◽  
Vol 37 (28) ◽  
Author(s):  
Stefano Moro ◽  
Magdalena Bacilieri ◽  
Francesca Deflorian ◽  
Giampiero Spalluto

2006 ◽  
Vol 30 (3) ◽  
pp. 301 ◽  
Author(s):  
Stefano Moro ◽  
Magdalena Bacilieri ◽  
Francesca Deflorian ◽  
Giampiero Spalluto

2004 ◽  
Vol 101 (31) ◽  
pp. 11304-11309 ◽  
Author(s):  
O. M. Becker ◽  
Y. Marantz ◽  
S. Shacham ◽  
B. Inbal ◽  
A. Heifetz ◽  
...  

2018 ◽  
Vol 16 (6) ◽  
pp. 786-848 ◽  
Author(s):  
Agostinho Lemos ◽  
Rita Melo ◽  
Antonio Jose Preto ◽  
Jose Guilherme Almeida ◽  
Irina Sousa Moreira ◽  
...  

2020 ◽  
Vol 11 ◽  
Author(s):  
Raise Ahmad ◽  
Julie E. Dalziel

Heterotrimeric G protein-coupled receptors (GPCRs) comprise the largest receptor family in mammals and are responsible for the regulation of most physiological functions. Besides mediating the sensory modalities of olfaction and vision, GPCRs also transduce signals for three basic taste qualities of sweet, umami (savory taste), and bitter, as well as the flavor sensation kokumi. Taste GPCRs reside in specialised taste receptor cells (TRCs) within taste buds. Type I taste GPCRs (TAS1R) form heterodimeric complexes that function as sweet (TAS1R2/TAS1R3) or umami (TAS1R1/TAS1R3) taste receptors, whereas Type II are monomeric bitter taste receptors or kokumi/calcium-sensing receptors. Sweet, umami and kokumi receptors share structural similarities in containing multiple agonist binding sites with pronounced selectivity while most bitter receptors contain a single binding site that is broadly tuned to a diverse array of bitter ligands in a non-selective manner. Tastant binding to the receptor activates downstream secondary messenger pathways leading to depolarization and increased intracellular calcium in TRCs, that in turn innervate the gustatory cortex in the brain. Despite recent advances in our understanding of the relationship between agonist binding and the conformational changes required for receptor activation, several major challenges and questions remain in taste GPCR biology that are discussed in the present review. In recent years, intensive integrative approaches combining heterologous expression, mutagenesis and homology modeling have together provided insight regarding agonist binding site locations and molecular mechanisms of orthosteric and allosteric modulation. In addition, studies based on transgenic mice, utilizing either global or conditional knock out strategies have provided insights to taste receptor signal transduction mechanisms and their roles in physiology. However, the need for more functional studies in a physiological context is apparent and would be enhanced by a crystallized structure of taste receptors for a more complete picture of their pharmacological mechanisms.


2011 ◽  
Vol 29 (5) ◽  
pp. 614-623 ◽  
Author(s):  
Santiago Vilar ◽  
Giulio Ferino ◽  
Sharangdhar S. Phatak ◽  
Barkin Berk ◽  
Claudio N. Cavasotto ◽  
...  

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