Published April 20, 2020 | Version v3

Supplementary data for publication "Mass-Resolved Electronic Circular Dichroism Ion Spectroscopy"

  • 1. INSERM, ARNA Laboratory, IECB, Pessac, France
  • 2. CNRS, Institut Européen de Chimie et Biologie, Pessac, France

Contributors

Project leader:

  • 1. INSERM
  • 2. CNRS

Description

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.

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.

Notes

raw data for a new figure (Figure 3) were added in this version

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Additional details

Related works

Cites
Preprint: arXiv:2002.01299 (arXiv)

Funding

European Commission
DNAFOLDIMS - Advanced mass spectrometry approaches to reveal nucleic acid folding energy landscapes 616551