52
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Changes in the Infrared Microspectroscopic Characteristics of DNA Caused by Cationic Elements, Different Base Richness and Single-Stranded Form

      research-article
      , *
      PLoS ONE
      Public Library of Science

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          The infrared (IR) analysis of dried samples of DNA and DNA-polypeptide complexes is still scarce. Here we have studied the FT-IR profiles of these components to further the understanding of the FT-IR signatures of chromatin and cell nuclei.

          Methodology/Principal Findings

          Calf thymus and salmon testis DNA, and complexes of histone H1, protamine, poly-L-lysine and poly-L-arginine (histone-mimic macromolecules) with DNA were analyzed in an IR microspectroscope equipped with an attenuated total reflection diamond objective and Grams software. Conditions including polypeptides bound to the DNA, DNA base composition, and single-stranded form were found to differently affect the vibrational characteristics of the chemical groups (especially, PO 2 ) in the nucleic acid. The antisymmetric stretching (ν as) of the DNA PO 2 was greater than the symmetric stretching (ν s) of these groups and increased in the polypeptide-DNA complexes. A shift of the ν as of the DNA PO 2 to a lower frequency and an increased intensity of this vibration were induced especially by lysine-rich histones. Lysine richness additionally contributed to an increase in the vibrational stretching of the amide I group. Even in simple molecules such as inorganic phosphates, the vibrational characteristics of the phosphate anions were differently affected by different cations. As a result of the optimization of the DNA conformation by binding to arginine-rich polypeptides, enhancements of the vibrational characteristics in the FT-IR fingerprint could be detected. Although different profiles were obtained for the DNA with different base compositions, this situation was no longer verified in the polypeptide-DNA complexes and most likely in isolated chromatin or cell nuclei. However, the ν as PO 2 s PO 2 ratio could discriminate DNA with different base compositions and DNA in a single-stranded form.

          Conclusions/Significance

          FT-IR spectral profiles are a valuable tool for establishing the vibrational characteristics of individualized chromatin components, such as DNA and DNA-polypeptide complexes in dried samples.

          Related collections

          Most cited references28

          • Record: found
          • Abstract: found
          • Article: not found

          A library of IR bands of nucleic acids in solution.

          This review presents a compilation and discussion of infrared (IR) bands characteristic of nucleic acids in various conformations. The entire spectral range 1800-800 cm(-1) relevant for DNA/RNA in aqueous solution has been subdivided into four sections. Each section contains descriptions of bands appearing from group specific parts of nucleic acid structure, such as nucleobase, base-sugar, sugar-phosphate and sugar moiety. The approach allows comparisons of information obtained from one spectral region with another. The IR band library should facilitate detailed and unambiguous assignment of structural changes, ligand binding, etc. in nucleic acids from IR spectra. is aimed at highlighting specific features that are useful for following major changes in nucleic acid structures. also concerns some recent results, where IR spectroscopy has been used to obtain semi-quantitative information on coexisting modes of sugar pucker in oligonucleotides.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Fourier transform IR spectroscopy of collagen and gelatin solutions: deconvolution of the amide I band for conformational studies.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Collagen type I amide I band infrared spectroscopy.

              Collagen fiber structure and organization have been found to vary in different tendon types. Differences have been reported in the FT-IR spectra of the amide I band of collagen-containing structures. In the present study, the FT-IR spectral characteristics of the amide I band of the bovine flexor tendon and the extended rat tail tendon were compared by using the diamond attenuated total reflectance technique. The objective was to associate FT-IR spectral characteristics in tendons with their different collagen fiber supraorganization and biomechanical properties. Nylon 6 and poly-L-lysine were used as polyamide models. Each of these materials was found to exhibit molecular order and crystallinity, as revealed by their birefringence. The following FT-IR parameters were evaluated: amide I band profile, absorption peaks and areas, and the 1655 cm⁻¹/1690 cm⁻¹ absorbance ratio. The amide I area and the 1655 cm⁻¹/1690 cm⁻¹ absorbance ratio were significantly higher for the bovine flexor tendon, indicating that its collagen fibers are richer in pyridinoline-type cross-linking, proline and/or hydroxyproline and H-bonding, and that these fibers are more packed and supraorganizationally ordered than those in the rat tail tendon. This conclusion is additionally supported by differences in collagen solubility and biochemical/biomechanical properties of the tendons. © 2010 Elsevier Ltd. All rights reserved.
                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                24 August 2012
                : 7
                : 8
                : e43169
                Affiliations
                [1]Department of Structural and Physiological Biology, Institute of Biology, University of Campinas (Unicamp), Campinas, São Paulo, Brazil
                University of Quebec at Trois-Rivieres, Canada
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: MLSM BCV. Performed the experiments: BCV. Analyzed the data: BCV MLSM. Contributed reagents/materials/analysis tools: BCV MLSM. Wrote the paper: MLSM BCV.

                Article
                PONE-D-12-14776
                10.1371/journal.pone.0043169
                3427352
                22937023
                82dcec22-f3f1-4a24-8266-4eff285d1cff
                Copyright @ 2012

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 23 May 2012
                : 20 July 2012
                Page count
                Pages: 12
                Funding
                This work was supported by grants no. 2010/50015-6 and 2007/58251-8 from the São Paulo State Research Foundation (FAPESP) and grant no. 472936/2009-7 from the Brazilian Council for Research and Development (CNPq). MLSM received a research fellowship from CNPq (301943/2009-5). The funders had no role in study deign, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Biochemistry
                Chemical Biology
                Macromolecular Assemblies
                Nucleic Acids
                Biophysics
                Biomacromolecule-Ligand Interactions
                Macromolecular Assemblies
                Nucleic Acids
                Molecular Cell Biology
                Chromosome Biology
                Chromatin
                Nucleic Acids
                DNA
                Nucleic Acid Components
                Chemistry
                Chemical Biology
                Physics
                Biophysics
                Macromolecular Assemblies
                Nucleic Acids
                Electromagnetic Radiation
                Infrared Radiation

                Uncategorized
                Uncategorized

                Comments

                Comment on this article