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3 results for “Circular dichroism spectroscopy”
External cavity quantum cascade laser vibrational circular dichroism spectroscopy for fast and sensitive analysis of proteins at low concentrations (Data analysis)
<p>This record contains a docker container image of the data evaluation shown in the publication "External cavity quantum cascade laser vibrational circular dichroism spectroscopy for fast and sensitive analysis of proteins at low concentrations". The evaluations can be accessed by running the container and accessing the contained Jupyter Lab via a browser. The calculations are contained in 'Eval_protein_D2O.ipynb'.</p> <p>To run the container (requires docker):</p> <p>1.download 'd2o_vcd.tar'</p> <p>2. in the command line, execute 'docker load -i d2o_vcd.tar'. This will return something like 'Loaded image: <image_name>' with image_name probably being "drhermann/vcd_d2o_00:trial_03"</p> <p>3. then 'docker run -p 8889:8889 <image_name>' replacing the brackets with the actual name of the image, such as drhermann/vcd_d2o_00:trial_03</p> <p>4.In your command line a link starting in 'http://127.0.0.1:8888/lab?token=...' will appear. Open this link in your browser to access the evaluation.</p>
Data for: Circular dichroism spectroscopy reveals multiple phytochrome photoproducts in equilibrium
Open the record for dataset details and reuse information.
Supplementary data for publication "Mass-Resolved Electronic Circular Dichroism Ion Spectroscopy"
<p>Research data for the main text and supporting information figures of publication "Mass-Resolved Electronic Circular Dichroism Ion Spectroscopy". Figure numbering according to arXiv preprint 2002.01299.</p> <p>Abstract: DNA and proteins are chiral: their three-dimensional structure cannot be superimposed with its mirror image. Circular dichroism spectroscopy is widely used to characterize chiral compounds, but data interpretation is difficult in the case of mixtures. We recorded the electronic circular dichroism spectra of DNA helices separated in a mass spectrometer. We studied guanine-rich strands having various secondary structures, electrosprayed them as negative ions, irradiated them with a UV-vis nanosecond OPO laser, and measured the difference in electron photodetachment efficiency between left and right circularly polarized light. The reconstructed circular dichroism ion spectra resemble their solution counterparts, thereby allowing us to assign the DNA helical topology. The ability to measure circular dichroism directly on biomolecular ions expands the capabilities of mass spectrometry for structural analysis.</p>
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