Telomere DNA G-quadruplex (2GKU) at neutral pH with LiCl
Data type: SASBDB experimental dataStatus: PublishedCurve type: SEC-SASLast updated: 2025-02-10T15:31:54.696467+01:00
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1. Samples, Components and Experimental Conditions Sample & Experiment
Sample 1 · Telomere DNA G-quadruplex (2GKU) at neutral pH with LiCl
Concentration
— – 4.8
Buffer / pH
6 mM Li2HPO4, 2 mM LiH2PO4, 1 mM EDTA, 185 mM LiCl, pH 7.2 / 7.2
Experimental temperature
22.0
Facility / beamline
Advanced Photon Source (APS), Argonne National Laboratory / BioCAT 18ID
Wavelength
0.1033 nm
Exposure
0.5 s × 2
Molecular Components
Component
Type / organism
UniProt and Construct
Oligomeric State
Molecular weight
Telomere DNA G-quadruplex Hybrid-1 formView sequence
TTGGGTTAGGGTTAGGGTTAGGGA
DNAsynthetic construct
——–—
monomerMolecule count 1
7.655 kDa
Experimental Curves
Curve
Points / columns
q range
Uncertainty quality
Negative-intensity points
Source file
1
1209[3]
0.00443014342–0.349695515 1/A
Has uncertainty columnMissing 0
9
sasbdb/entries/63/sasdw63/source/SASDW63.dat
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2. Measurements Reported by SASBDB Reported Results
Metric
Method
Value
Uncertainty
Unit
dmax
P(r)
4.3
—
Å
i0
Guinier
0.0166437
—
1/cm
i0
P(r)
0.01666
—
1/cm
mw
Experimental
9.0
—
kDa
porod_volume
Porod
7.1
—
ų
rg
Guinier
1.192
0.016
Å
rg
P(r)
1.2
—
Å
These values are reported by SASBDB; SAXSdb did not recalculate them from the experimental curve.
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3. Source Fits and Models Source Fits & Models
This entry has no source fit record.
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4. Source File Index Source Files
Category
Path
Download status
Size
curve
sasbdb/entries/63/sasdw63/source/SASDW63.dat
downloaded
59790
full_entry_zip
sasbdb/entries/63/sasdw63/source/SASDW63.zip
downloaded
48281
pddf
sasbdb/entries/63/sasdw63/source/SASDW63.out
downloaded
104063
sascif
sasbdb/entries/63/sasdw63/source/SASDW63.sascif
not_available
—
summary
sasbdb/entries/63/sasdw63/source/summary.json
downloaded
6168
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5. Experiment Description and Publication Experiment & Publication
Original Experiment Description
Synchrotron SAXS data from solutions of Telomere DNA G-quadruplex (2GKU) in 6 mM Li2HPO4, 2 mM LiH2PO4, 1 mM EDTA, 185 mM LiCl, pH 7.2, pH 7.2 were collected on the BioCAT 18ID beam line at the Advanced Photon Source (APS), Argonne National Laboratory (Lemont, IL, USA) using a Pilatus3 X 1M detector at a sample-detector distance of 3.7 m and at a wavelength of λ = 0.1033 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 250.00 μl sample at 4.8 mg/ml was injected at a 0.60 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 22°C. Two successive 0.500 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
Related Publication
Title
Early events in G-quadruplex folding captured by time-resolved small-angle X-ray scattering.
Synchrotron SAXS data from solutions of Telomere DNA G-quadruplex (2GKU) in 6 mM Li2HPO4, 2 mM LiH2PO4, 1 mM EDTA, 185 mM LiCl, pH 7.2, pH 7.2 were collected on the BioCAT 18ID beam line at the Advanced Photon Source (APS), Argonne National Laboratory (Lemont, IL, USA) using a Pilatus3 X 1M detector at a sample-detector distance of 3.7 m and at a wavelength of λ = 0.1033 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 250.00 μl sample at 4.8 mg/ml was injected at a 0.60 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 22°C. Two successive 0.500 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.