TY - JOUR
T1 - Continental and Antarctic Lichens
T2 - isolation, identification and molecular modeling of the depside tenuiorin from the Antarctic lichen Umbilicaria antarctica as tau protein inhibitor
AU - Salgado, Francisco
AU - Caballero, Julio
AU - Vargas, Reinaldo
AU - Cornejo, Alberto
AU - Areche, Carlos
PY - 2018/1/1
Y1 - 2018/1/1
N2 - Alzheimer´s disease (AD) is the most common form of dementia involving Aβ and tau protein. So far, AD cure remains elusive, but considering that AD progresses throughout tau pathology, which turns tau protein an appropriate target, besides tau is also included in other neurodegenerative disorders named as tauopathies. Here, we have isolated seventeen compounds belonging to six lichens species. Due to scarce of spectroscopic data of the compound 5,7-dihydroxy-6-methylphthalide, we explained their structural elucidation based on NMR data. In this study, we show that only tenuiorin from Umbilicaria antarctica inhibited 50% of tau 4R at 100 µM. Then, we shown that molecular interactions of tenuiorin with the steric zipper model of the hexapeptide 306VQIVYK311 were studied by docking calculations and the results suggested that tenuiorin forms both hydrogen bonds with lysine and glutamine side chains and forms several hydrophobic interactions with valine and lysine from 306VQIVYK311 motif. (Figure presented.).
AB - Alzheimer´s disease (AD) is the most common form of dementia involving Aβ and tau protein. So far, AD cure remains elusive, but considering that AD progresses throughout tau pathology, which turns tau protein an appropriate target, besides tau is also included in other neurodegenerative disorders named as tauopathies. Here, we have isolated seventeen compounds belonging to six lichens species. Due to scarce of spectroscopic data of the compound 5,7-dihydroxy-6-methylphthalide, we explained their structural elucidation based on NMR data. In this study, we show that only tenuiorin from Umbilicaria antarctica inhibited 50% of tau 4R at 100 µM. Then, we shown that molecular interactions of tenuiorin with the steric zipper model of the hexapeptide 306VQIVYK311 were studied by docking calculations and the results suggested that tenuiorin forms both hydrogen bonds with lysine and glutamine side chains and forms several hydrophobic interactions with valine and lysine from 306VQIVYK311 motif. (Figure presented.).
KW - Alzheimer´s disease
KW - Lichens
KW - Tau protein
UR - http://www.scopus.com/inward/record.url?scp=85056102272&partnerID=8YFLogxK
U2 - 10.1080/14786419.2018.1492576
DO - 10.1080/14786419.2018.1492576
M3 - Article
AN - SCOPUS:85056102272
SN - 1478-6419
VL - 34
SP - 646
EP - 650
JO - Natural Product Research
JF - Natural Product Research
IS - 5
ER -