Towards a Precise NMR Quantification of Acute Phase Inflammation Proteins from Human Serum

Author:

Mallagaray Alvaro1ORCID,Rudolph Lorena1ORCID,Lindloge Melissa1ORCID,Mölbitz Jarne1ORCID,Thomsen Henrik1ORCID,Schmelter Franziska2ORCID,Alhabash Mohamad Ward1ORCID,Abdullah Mohammed R.3ORCID,Saraei Roza45,Ehlers Marc2ORCID,Graf Tobias45,Sina Christian26,Petersmann Astrid37,Nauck Matthias38ORCID,Günther Ulrich L.1ORCID

Affiliation:

1. Institute of Chemistry and Metabolomics University of Lübeck Ratzeburger Allee 160 23562 Lübeck Germany

2. Institute of Nutritional Medicine University of Lübeck and Medical Center Schleswig-Holstein Campus Lübeck Ratzeburger Allee 160 23538 Lübeck Germany

3. Institute of Clinical Chemistry and Laboratory Medicine Greifswald University Hospital Fleischmannstraße 8 17475 Greifswald Germany

4. Department of Cardiology Angiology and Intensive Care Medicine University Heart Center Lübeck Ratzeburger Allee 160 23538 Lübeck Germany

5. German Centre for Cardiogenic Vascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck Lübeck Germany

6. Fraunhofer Research Institution for Individualized and Cell-Based Medical Engineering (IMTE) Mönkhofer Weg 239 a 23538 Lübeck Germany

7. Institute of Clinical Chemistry and Laboratory Medicine Carl von Ossietzky University Ammerländer Heerstraße 114–118 26129 Oldenburg Germany

8. German Centre for Cardiogenic Vascular Research (DZHK) Partner Site Greifswald University Medicine Greifswald Germany

Abstract

AbstractNuclear Magnetic Resonance (NMR) spectra of human serum and plasma show, besides metabolites and lipoproteins, two characteristic signals termed GlycA and B arising from the acetyl groups of glycoprotein glycans from acute phase proteins, which constitute good markers for inflammatory processes. Here, we report a comprehensive assignment of glycoprotein glycan NMR signals observed in human serum, showing that GlycA and GlycB signals originate from Neu5Ac and GlcNAc moieties from N‐glycans, respectively. Diffusion‐edited NMR experiments demonstrate that signal components can be associated with specific acute phase proteins. Conventionally determined concentrations of acute phase glycoproteins correlate well with distinct features in NMR spectra (R2 up to 0.9422, p‐value <0.001), allowing the simultaneous quantification of several acute phase inflammation proteins. Overall, a proteo‐metabolomics NMR signature of significant diagnostic potential is obtained within 10–20 min acquisition time. This is exemplified in serum samples from COVID‐19 and cardiogenic shock patients showing significant changes in several acute phase proteins compared to healthy controls.

Publisher

Wiley

Subject

General Medicine

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