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Unravelling structural information from complex mixtures utilizing correlation spectroscopy applied to HSQC spectra. | LitMetric

AI Article Synopsis

  • - The report introduces HSQC correlation spectroscopy (HSQCcos), a new method that utilizes statistical correlation to obtain chemical information from 2D-HSQC spectra, showcasing its application on heparin, a complex polysaccharide.
  • - HSQCcos helped uncover structural details related to heparin's diverse components, revealing a bifurcated signal for a specific glucosamine position due to its unique interactions within the molecule's structure.
  • - The method also revealed insights into rare disaccharide sequences in heparin, indicating the presence of a disaccharide with a free amine near the linkage region, demonstrating HSQCcos's potential to analyze complex mixtures effectively.

Article Abstract

The first use of statistical correlation spectroscopy to extract chemical information from 2D-HSQC spectra, termed HSQC correlation spectroscopy (HSQCcos), is reported. HSQCcos is illustrated using heparin, a heterogeneous polysaccharide, whose diverse composition causes signals in HSQC spectra to disperse. HSQCcos has been used to probe the chain modifications that cause this effect and reveals hitherto unreported structural details. An interesting finding was that the signal for position 2 of trisulfated glucosamine [N-, 3-O-, and 6-O-sulfated] (A*) is bifurcated, owing to the presence of A* residues in both the "normal" antithrombin binding site and also at the nonreducing end of the molecule, which is reported in intact heparin for the first time. The method was also applied to investigating the environment around other rare sequences/disaccharides, suggesting that the disaccharide; 2-O-sulfated iduronic acid linked to 6-O-sulfated N-glucosamine, which contains a free amine at position 2, is adjacent to the heparin linkage region. HSQCcos can extract chemically related signals from information-rich spectra obtained from complex mixtures such as heparin.

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Source
http://dx.doi.org/10.1021/ac4014379DOI Listing

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