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NMR processing:
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MARS
UNIO Match
PINE
Side-chains:
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NOEs:
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UNIO Candid
ASDP
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Ab initio:
GeNMR
Cyana
XPLOR-NIH
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UNIO ATNOS-Candid
UNIO Candid
Fragment-based:
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GeNMR
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WeNMR CS-Rosetta
BMRB CS-Rosetta
Homology-based:
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Torsion angles from chemical shifts:
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Promega- Proline
Secondary structure from chemical shifts:
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TALOS
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d2D
PECAN
Flexibility from chemical shifts:
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Interactions from chemical shifts:
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UNIO Shiftinspector
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RefDB
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RPF scores
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Vasco
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RDCs:
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SAVES2 or SAVES4
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From structure:
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ArShift- Aromatic
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Proshift
PPM
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From sequence:
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Camcoil
Poulsen_rc_CS
Disordered proteins:
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Format conversion & validation:
CCPN
From NMR-STAR 3.1
Validate NMR-STAR 3.1
NMR sample preparation:
Protein disorder:
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Protein solubility:
camLILA
ccSOL
Camfold
camGroEL
Zyggregator
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Old 10-20-2017, 01:48 PM
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Default NMR based structural studies decipher stacking of the alkaloid coralyne to terminal guanines at two different sites in parallel G-quadruplex DNA, [d(TTGGGGT)]4 and [d(TTAGGGT)]4.

NMR based structural studies decipher stacking of the alkaloid coralyne to terminal guanines at two different sites in parallel G-quadruplex DNA, [d(TTGGGGT)]4 and [d(TTAGGGT)]4.

Related Articles NMR based structural studies decipher stacking of the alkaloid coralyne to terminal guanines at two different sites in parallel G-quadruplex DNA, [d(TTGGGGT)]4 and [d(TTAGGGT)]4.

Biochim Biophys Acta. 2017 02;1861(2):37-48

Authors: Padmapriya K, Barthwal R

Abstract
BACKGROUND: Telomere elongation by telomerase gets inhibited by G-quadruplex DNA found in its guanine rich region. Stabilization of G-quadruplex DNA upon ligand binding has evolved as a promising strategy to target cancer cells in which telomerase is over expressed.
METHODS: Interaction of anti-leukemic alkaloid, coralyne, to tetrameric parallel [d(TTGGGGT)]4 (Ttel7), [d(TTAGGGT)]4 (Htel7) and monomeric anti-parallel [dGGGG(TTGGGG)3] (Ttel22) G-quadruplex DNA has been studied using Circular Dichroism (CD) spectroscopy. Titrations of coralyne with Ttel7 and Htel7 were monitored by (1)H and (31)P NMR spectroscopy. Solution structure of coralyne-Ttel7 complex was obtained by restrained Molecular Dynamics (rMD) simulations using distance restraints from 2D NOESY spectra. Thermal stabilization of DNA was determined by absorption, CD and (1)H NMR.
RESULTS AND CONCLUSIONS: Binding of coralyne to Ttel7/Htel7 induces negative CD band at 315/300nm. A significant upfield shift in all GNH, downfield shift in T2/T7 base protons and upfield shift (1.8ppm) in coralyne protons indicates stacking interactions. (31)P chemical shifts and NOE contacts of G3, G6, T2, T7 protons with methoxy protons reveal proximity of coralyne to T2pG3 and G6pT7 sites. Solution structure reveals stacking of coralyne at G6pT7 and T2pG3 steps with two methoxy groups of coralyne located in the grooves along with formation of a hydrogen bond. Binding stabilizes Ttel7/Htel7 by ~25-35°C in 2:1 coralyne-Ttel7/Htel7 complex.
GENERAL SIGNIFICANCE: The present study is the first report on solution structure of coralyne-Ttel7 complex showing stacking of coralyne with terminal guanine tetrads leading to significant thermal stabilization, which may be responsible for telomerase inhibition.


PMID: 27838396 [PubMed - indexed for MEDLINE]



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