NMR structure of dual site binding of mitoxantrone dimer to opposite grooves of parallel stranded G-quadruplex [d-(TTGGGGT)]4

Biochimie ◽  
2016 ◽  
Vol 128-129 ◽  
pp. 59-69 ◽  
Author(s):  
Tarikere Palakshan Pradeep ◽  
Ritu Barthwal
2015 ◽  
Vol 26 (6) ◽  
pp. 705-708 ◽  
Author(s):  
Li-Jia Yu ◽  
Wei Gai ◽  
Qian-Fan Yang ◽  
Jun-Feng Xiang ◽  
Hong-Xia Sun ◽  
...  

ACS Omega ◽  
2021 ◽  
Vol 6 (4) ◽  
pp. 2613-2625
Author(s):  
Mukti Mohammad ◽  
Harun Al Rasid Gazi ◽  
Kumud Pandav ◽  
Prateek Pandya ◽  
Md. Maidul Islam

2020 ◽  
Vol 48 (6) ◽  
pp. 3315-3327 ◽  
Author(s):  
Arijit Maity ◽  
Fernaldo Richtia Winnerdy ◽  
Weili Denyse Chang ◽  
Gang Chen ◽  
Anh Tuân Phan

Abstract G-rich DNA sequences with tracts of three or more continuous guanines (G≥3) are known to have high propensity to adopt stable G-quadruplex (G4) structures. Bioinformatic analyses suggest high prevalence of G-rich sequences with short G-tracts (G≤2) in the human genome. However, due to limited structural studies, the folding principles of such sequences remain largely unexplored and hence poorly understood. Here, we present the solution NMR structure of a sequence named AT26 consisting of irregularly spaced G2 tracts and two isolated single guanines. The structure is a four-layered G4 featuring two bi-layered blocks, locked between themselves in an unprecedented fashion making it a stable scaffold. In addition to edgewise and propeller-type loops, AT26 also harbors two V-shaped loops: a 2-nt V-shaped loop spanning two G-tetrad layers and a 0-nt V-shaped loop spanning three G-tetrad layers, which are named as VS- and VR-loop respectively, based on their distinct structural features. The intra-lock motif can be a basis for extending the G-tetrad core and a very stable intra-locked G4 can be formed by a sequence with G-tracts of various lengths including several G2 tracts. Findings from this study will aid in understanding the folding of G4 topologies from sequences containing irregularly spaced multiple short G-tracts.


Molecules ◽  
2020 ◽  
Vol 25 (15) ◽  
pp. 3341
Author(s):  
Georgi Stavrakov ◽  
Irena Philipova ◽  
Atanas Lukarski ◽  
Mariyana Atanasova ◽  
Dimitrina Zheleva ◽  
...  

Galantamine (GAL) and curcumin (CU) are alkaloids used to improve symptomatically neurodegenerative conditions like Alzheimer’s disease (AD). GAL acts mainly as an inhibitor of the enzyme acetylcholinesterase (AChE). CU binds to amyloid-beta (Aβ) oligomers and inhibits the formation of Aβ plaques. Here, we combine GAL core with CU fragments and design a combinatorial library of GAL-CU hybrids as dual-site binding AChE inhibitors. The designed hybrids are screened for optimal ADME properties and BBB permeability and docked on AChE. The 14 best performing compounds are synthesized and tested in vitro for neurotoxicity and anti-AChE activity. Five of them are less toxic than GAL and CU and show activities between 41 and 186 times higher than GAL.


2017 ◽  
Vol 129 (25) ◽  
pp. 7208-7212 ◽  
Author(s):  
Julia Wirmer-Bartoschek ◽  
Lars Erik Bendel ◽  
Hendrik R. A. Jonker ◽  
J. Tassilo Grün ◽  
Francesco Papi ◽  
...  

2005 ◽  
Vol 157-158 ◽  
pp. 414-415
Author(s):  
Maurizio Recanatini ◽  
Andrea Cavalli ◽  
Giovanni Bottegoni

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