Beyond uniform screening: electrostatic heterogeneity dictates solution structure of complex macromolecules
Fuente:
arXiv
Saved in:
| Main Authors: | , , , , , , , , , |
|---|---|
| Format: | Preprint |
| Published: |
2026
|
| Subjects: | |
| Online Access: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1866911372126715904 |
|---|---|
| author | Camerin, Fabrizio Polimeni, Marco Tavagnacco, Letizia Everts, Jeffrey C. Saringer, Szilard Gulotta, Alessandro Skar-Gislinge, Nicholas Stradner, Anna Zaccarelli, Emanuela Schurtenberger, Peter |
| author_facet | Camerin, Fabrizio Polimeni, Marco Tavagnacco, Letizia Everts, Jeffrey C. Saringer, Szilard Gulotta, Alessandro Skar-Gislinge, Nicholas Stradner, Anna Zaccarelli, Emanuela Schurtenberger, Peter |
| contents | The complexity of biomolecular interactions necessitates advanced methodologies to accurately capture their behavior in solution. In this work, we focus on monoclonal antibodies and adopt a multi-scale coarse-graining strategy for their modeling, with particular emphasis on the role of electrostatic interactions. Using scattering experiments, theoretical analysis, and large-scale computer simulations, we explicitly compare two selected case studies-markedly different in their charge distributions. Through mutually corroborating lines of evidence, we demonstrate that conventional approaches relying on electrostatic screening and implicit charge representations fail to capture the structural and thermodynamic properties of antibody solutions when strong charge heterogeneity is present, even at a moderate (amino acid) level of coarse-graining. These findings highlight the importance of a correct treatment of electrostatic interactions and ion screening for heterogeneously- and oppositely-charged colloidal and protein systems. Such considerations are essential to move beyond descriptive models towards a truly predictive framework, with direct implications for the formulation of therapeutics and the treatment of other complex soft-matter systems. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2601_08544 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | Beyond uniform screening: electrostatic heterogeneity dictates solution structure of complex macromolecules Camerin, Fabrizio Polimeni, Marco Tavagnacco, Letizia Everts, Jeffrey C. Saringer, Szilard Gulotta, Alessandro Skar-Gislinge, Nicholas Stradner, Anna Zaccarelli, Emanuela Schurtenberger, Peter Soft Condensed Matter Biological Physics The complexity of biomolecular interactions necessitates advanced methodologies to accurately capture their behavior in solution. In this work, we focus on monoclonal antibodies and adopt a multi-scale coarse-graining strategy for their modeling, with particular emphasis on the role of electrostatic interactions. Using scattering experiments, theoretical analysis, and large-scale computer simulations, we explicitly compare two selected case studies-markedly different in their charge distributions. Through mutually corroborating lines of evidence, we demonstrate that conventional approaches relying on electrostatic screening and implicit charge representations fail to capture the structural and thermodynamic properties of antibody solutions when strong charge heterogeneity is present, even at a moderate (amino acid) level of coarse-graining. These findings highlight the importance of a correct treatment of electrostatic interactions and ion screening for heterogeneously- and oppositely-charged colloidal and protein systems. Such considerations are essential to move beyond descriptive models towards a truly predictive framework, with direct implications for the formulation of therapeutics and the treatment of other complex soft-matter systems. |
| title | Beyond uniform screening: electrostatic heterogeneity dictates solution structure of complex macromolecules |
| topic | Soft Condensed Matter Biological Physics |
| url | https://arxiv.org/abs/2601.08544 |