Literature DB >> 16810455

Natural sweet macromolecules: how sweet proteins work.

P A Temussi1.   

Abstract

A few proteins, discovered mainly in tropical fruits, have a distinct sweet taste. These proteins have played an important role towards a molecular understanding of the mechanisms of taste. Owing to the huge difference in size, between most sweeteners and sweet proteins, it was believed that they must interact with a different receptor from that of small molecular weight sweeteners. Recent modelling studies have shown that the single sweet taste receptor has multiple active sites and that the mechanism of interaction of sweet proteins is intrinsically different from that of small sweeteners. Small molecular weight sweeteners occupy small receptor cavities inside two subdomains of the receptor, whereas sweet proteins can interact with the sweet receptor according to a mechanism called the 'wedge model' in which they bind to a large external cavity. This review describes these mechanisms and outlines a history of sweet proteins.

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Year:  2006        PMID: 16810455     DOI: 10.1007/s00018-006-6077-8

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  10 in total

1.  High-resolution structure of the recombinant sweet-tasting protein thaumatin I.

Authors:  Tetsuya Masuda; Keisuke Ohta; Bunzo Mikami; Naofumi Kitabatake
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2011-05-24

2.  A preliminary neutron crystallographic study of thaumatin.

Authors:  Susana C M Teixeira; Matthew P Blakeley; Ricardo M F Leal; Edward P Mitchell; V Trevor Forsyth
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2008-04-05

3.  Reduced sweetness of a monellin (MNEI) mutant results from increased protein flexibility and disruption of a distant poly-(L-proline) II helix.

Authors:  Catherine M Templeton; Saeideh Ostovar pour; Jeanette R Hobbs; Ewan W Blanch; Steven D Munger; Graeme L Conn
Journal:  Chem Senses       Date:  2011-02-22       Impact factor: 3.160

4.  Key amino acid residues involved in multi-point binding interactions between brazzein, a sweet protein, and the T1R2-T1R3 human sweet receptor.

Authors:  Fariba M Assadi-Porter; Emeline L Maillet; James T Radek; Jeniffer Quijada; John L Markley; Marianna Max
Journal:  J Mol Biol       Date:  2010-03-17       Impact factor: 5.469

5.  Dietary proteins and food-related reward signals.

Authors:  Katri Peuhkuri; Nora Sihvola; Riitta Korpela
Journal:  Food Nutr Res       Date:  2011-06-01       Impact factor: 3.894

6.  Monellin (MNEI) at 1.15 A resolution.

Authors:  J R Hobbs; S D Munger; G L Conn
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2007-02-13

7.  New Insight Into the Structure-Activity Relationship of Sweet-Tasting Proteins: Protein Sector and Its Role for Sweet Properties.

Authors:  Xiangzhong Zhao; Congrui Wang; Yue Zheng; Bo Liu
Journal:  Front Nutr       Date:  2021-06-18

8.  Positive Charges on the Surface of Thaumatin Are Crucial for the Multi-Point Interaction with the Sweet Receptor.

Authors:  Tetsuya Masuda; Satomi Kigo; Mayuko Mitsumoto; Keisuke Ohta; Mamoru Suzuki; Bunzo Mikami; Naofumi Kitabatake; Fumito Tani
Journal:  Front Mol Biosci       Date:  2018-02-13

Review 9.  Alteration, Reduction and Taste Loss: Main Causes and Potential Implications on Dietary Habits.

Authors:  Davide Risso; Dennis Drayna; Gabriella Morini
Journal:  Nutrients       Date:  2020-10-27       Impact factor: 5.717

10.  A Super Stable Mutant of the Plant Protein Monellin Endowed with Enhanced Sweetness.

Authors:  Masoud Delfi; Alessandro Emendato; Serena Leone; Eros Antonio Lampitella; Piero Porcaro; Gaetano Cardinale; Luigi Petraccone; Delia Picone
Journal:  Life (Basel)       Date:  2021-03-12
  10 in total

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