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What unique features are observed in T = 7 capsid structures of dsDNA viruses?
What unique features are observed in T = 7 capsid structures of dsDNA viruses?
Answered
T = 7 capsid structures of dsDNA viruses exhibit several unique features that distinguish them from other viral capsid structures. Here are the key characteristics:
- Pentamer and Hexamer Arrangement: T = 7 capsids typically consist of 72 pentamers and a varying number of hexamers. In the case of dsDNA viruses, the arrangement of these pentamers and hexamers allows for a complex and stable structure that can accommodate the viral genome.
- Non-Identical Subunits: Unlike some other viral capsids that rely on a uniform set of identical subunits, T = 7 capsids can incorporate non-identical subunits. For example, in the SV40 capsid, 60 of the pentamers are situated in positions typically occupied by hexamers, demonstrating a unique adaptation of the capsid structure.
- C-Terminal Arm Flexibility: The C-terminal arms of the capsid proteins in T = 7 dsDNA viruses often exhibit significant flexibility. This flexibility allows the arms to interact with neighboring subunits in a dynamic manner, facilitating the assembly process and contributing to the overall stability of the capsid.
- Quasi-Symmetry: T = 7 capsids are characterized by quasi-symmetry, which allows for variations in the arrangement of subunits while maintaining a stable and functional structure. This quasi-symmetry is essential for accommodating the structural requirements of the viral genome and ensuring proper assembly.
- Diverse Protein Interactions: The interactions between the capsid proteins in T = 7 structures can be quite complex, involving both covalent and non-covalent interactions. These interactions help to stabilize the capsid and ensure that it can withstand the pressures of encapsidating the viral genome.
- Unique Structural Domains: The capsid proteins in T = 7 dsDNA viruses often contain unique structural domains that contribute to their assembly and stability. For example, the presence of β-barrel structures or helix bundles can play a critical role in the overall architecture of the capsid.
- High Fidelity Assembly: The assembly of T = 7 capsids often involves high-fidelity interactions between subunits, which are crucial for maintaining the integrity of the capsid. This is particularly important for dsDNA viruses, as the capsid must effectively protect the viral genome.
- Calcium and RNA Binding Sites: In some T = 7 capsids, specific binding sites for calcium ions and RNA are preserved at the interfaces between subunits. These binding sites can play a role in stabilizing the capsid structure and facilitating interactions with the viral genome.
- Pleomorphic Properties: Some T = 7 capsids exhibit pleomorphic properties, meaning they can adopt multiple shapes or forms. This can be influenced by the local chemical environment and the specific interactions between subunits.
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