| Title: | Application of NMR spectroscopy for studies of self-association and aggregation in protein formulations |
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| Authors: | ID Zalar, Matja (Author)
ID Bramham, Jack E. (Author)
ID Golovanov, Alexander P. (Author) |
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| Files: |  1-s2.0-S0079656526000178-main.pdf (6,98 MB)
MD5: 48BF26B86F07868C49C07C3B9A41FF9F
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| Language: | English |
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| Work type: | Article |
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| Typology: | 1.01 - Original Scientific Article |
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| Organization: | FKKT - Faculty of Chemistry and Chemical Engineering
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| Abstract: | Protein self-association and aggregation are common phenomena that occur in various environments, including live cells, research samples, and during bioprocessing or storage of biopharmaceuticals. They may be a part of native biological function, or cause diseases, it can be an artefact in protein research, a concerning phenomenon in biopharmaceutical protein formulation, or a favourable opportunity to spontaneously concentrate proteins. The consequences of protein self-association and aggregation vary across different fields, and therefore may require somewhat different analytical approaches for their assessment and characterization. In this review we focus on types of aggregation and self-association which occur in protein formulations prepared for diverse purposes, where the aggregation itself is not the main functional feature of a protein. We aim to first highlight some major pathways of protein self-interaction and outline the terminology around the process of protein molecules clumping together, and the level of structural changes involved for each major pathway. We will briefly overview various analytical methods for characterising protein aggregation and self-association, and then consider the role of NMR, highlighting NMR parameters that are frequently used to gain insight into these processes. We focus on signal line broadening, chemical shift perturbation, diffusion coefficients, relaxation parameters and spatially selective NMR as the main approaches used to characterise various protein particles and the kinetics of their formation. Lastly, we discuss in more detail a few recent examples of NMR applications to study protein self-association and aggregation mainly in biopharmaceutical context, of how NMR measurables can assist in profiling of higher-order-structure, studies of protein-excipient interactions in formulation development, study of liquid-liquid phase separation and assessment of protein behaviour in complex mixtures. We also discuss low-field NMR methods that are being developed for in-line process monitoring as well as quality control. |
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| Keywords: | biopharmaceuticals, protein aggregation, prote, ATPsdelf-association, co-solvents, excipients, NMR |
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| Publication status: | Published |
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| Publication version: | Version of Record |
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| Submitted for review: | 05.12.2025 |
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| Article acceptance date: | 22.05.2026 |
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| Publication date: | 25.05.2026 |
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| Publisher: | Elsevier B.V. |
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| Year of publishing: | 2026 |
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| Number of pages: | 28 str. |
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| Numbering: | Vol. 156/157, article no.] 101611 |
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| PID: | 20.500.12556/DKUM-98515  |
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| UDC: | 543.384 |
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| ISSN on article: | 1873-3301 |
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| COBISS.SI-ID: | 281382147 |
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| Copyright: | © 2026 The Authors |
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| Publication date in DKUM: | 17.06.2026 |
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| Views: | 173 |
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| Downloads: | 8 |
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| Metadata: |    |
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| Categories: | Misc.
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