Structure-based screening for discovery of sweet compounds.

Abstract:

:Sweet taste is a cue for calorie-rich food and is innately attractive to animals, including humans. In the context of modern diets, attraction to sweetness presents a significant challenge to human health. Most known sugars and sweeteners bind to the Venus Fly Trap domain of T1R2 subunit of the sweet taste heterodimer. Because the sweet taste receptor structure has not been experimentally solved yet, a possible approach to finding sweet molecules is virtual screening using compatibility of candidate molecules to homology models of sugar-binding site. Here, the constructed structural models, docking and scoring schemes were validated by their ability to rank known sweet-tasting compounds higher than properties-matched random molecules. The best performing models were next used in virtual screening, retrieving recently patented sweeteners and providing novel predictions.

journal_name

Food Chem

journal_title

Food chemistry

authors

Ben Shoshan-Galeczki Y,Niv MY

doi

10.1016/j.foodchem.2020.126286

subject

Has Abstract

pub_date

2020-06-15 00:00:00

pages

126286

eissn

0308-8146

issn

1873-7072

pii

S0308-8146(20)30134-5

journal_volume

315

pub_type

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