Studying the ssDNA loaded adeno-associated virus aggregation using coarse-grained molecular dynamics simulations
Copyright © 2024 Elsevier B.V. All rights reserved..
The aggregation of adeno-associated viral (AAV) capsids in an aqueous environment was investigated via coarse-grained molecular dynamics (CG-MD) simulations. The primary driving force and mechanism of the aggregation were investigated with or without single-strand DNA (ssDNA) loaded at various process temperatures. Capsid aggregation appeared to involve multiple residue interactions (i.e., hydrophobic, polar and charged residues) leading to complex protein aggregation. In addition, two aggregation mechanisms (i.e., the fivefold face-to-face contact and the edge-to-edge contact) were identified from this study. The ssDNA with its asymmetric structure could be the reason for destabilizing protein subunits and enhancing the interaction between the charged residues, and further result in the non-reversible face-to-face contact. At higher temperature, the capsid structure was found to be unstable with the significant size expansion of the loaded ssDNA which could be attributed to reduced number of intramolecular hydrogen bonds, the increased conformational deviations of protein subunits and the higher residue fluctuations. The CG-MD model was further validated with previous experimental and simulation data, including the full capsid size measurement and the capsid internal pressure. Thus, a good understanding of AAV capsid aggregation, instability and the role of ssDNA were revealed by applying the developed computational model.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:655 |
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| Enthalten in: |
International journal of pharmaceutics - 655(2024) vom: 25. Apr., Seite 123985 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Duran, Tibo [VerfasserIn] |
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| Links: |
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| Themen: |
Adeno-associated virus |
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| Anmerkungen: |
Date Completed 15.04.2024 Date Revised 15.04.2024 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1016/j.ijpharm.2024.123985 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM369745469 |
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| 520 | |a Copyright © 2024 Elsevier B.V. All rights reserved. | ||
| 520 | |a The aggregation of adeno-associated viral (AAV) capsids in an aqueous environment was investigated via coarse-grained molecular dynamics (CG-MD) simulations. The primary driving force and mechanism of the aggregation were investigated with or without single-strand DNA (ssDNA) loaded at various process temperatures. Capsid aggregation appeared to involve multiple residue interactions (i.e., hydrophobic, polar and charged residues) leading to complex protein aggregation. In addition, two aggregation mechanisms (i.e., the fivefold face-to-face contact and the edge-to-edge contact) were identified from this study. The ssDNA with its asymmetric structure could be the reason for destabilizing protein subunits and enhancing the interaction between the charged residues, and further result in the non-reversible face-to-face contact. At higher temperature, the capsid structure was found to be unstable with the significant size expansion of the loaded ssDNA which could be attributed to reduced number of intramolecular hydrogen bonds, the increased conformational deviations of protein subunits and the higher residue fluctuations. The CG-MD model was further validated with previous experimental and simulation data, including the full capsid size measurement and the capsid internal pressure. Thus, a good understanding of AAV capsid aggregation, instability and the role of ssDNA were revealed by applying the developed computational model | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Adeno-associated virus | |
| 650 | 4 | |a Aggregation | |
| 650 | 4 | |a Coarse-grained | |
| 650 | 4 | |a Molecular dynamics simulations | |
| 650 | 4 | |a Sing-strand DNA | |
| 650 | 7 | |a Protein Subunits |2 NLM | |
| 650 | 7 | |a DNA, Single-Stranded |2 NLM | |
| 700 | 1 | |a Naik, Shivangi |e verfasserin |4 aut | |
| 700 | 1 | |a Sharifi, Leila |e verfasserin |4 aut | |
| 700 | 1 | |a DiLuzio, Willow R |e verfasserin |4 aut | |
| 700 | 1 | |a Chanda, Arani |e verfasserin |4 aut | |
| 700 | 1 | |a Chaudhuri, Bodhisattwa |e verfasserin |4 aut | |
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