Helical Capsids

Helical capsids are protein shells that package and protect viral genetic material by arranging capsid subunits in a spiral or helical pattern. In this architecture, repeated interactions between coat proteins and nucleic acid generate a flexible, elongated structure whose length can depend on the genome and the number of associated subunits. Helical capsids occur in viruses infecting plants, animals, and bacteria, and their organization helps researchers understand viral assembly, stability, and host-cell entry. Studying these structures also informs antiviral research, virus-like particle design, nanotechnology, and the development of microscopy and structural biology methods.

Helical Capsids - Related Videos

Research

JoVE Journal - Immunology and Infection
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Structure of HIV-1 Capsid Assemblies by Cryo-electron Microscopy and Iterative Helical Real-space Reconstruction

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Cited by 8 •

2011

This article describes a method to obtain a three-dimensional (3D) structure of helically assembled molecules using cryo-electron microscopy. In this protocol, we use HIV-1 capsid assemblies to illustrate the detailed 3D reconstruction procedure for achieving a density map by the iterative helical real-space reconstruction method.

Research

JoVE EoE - Viral Growth and Techniques

Visualizing Heat-Treated Viral Capsids Using Transmission Electron Microscopy

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2026

Source: Moore, M. D., et al. Alternative In Vitro Methods for the Determination of Viral Capsid Structural Integrity. J. Vis. Exp.(2017).This video demonstrates how purified viral capsids are heat-treated, prepared, and imaged using transmission electron microscopy (TEM) to reveal structural changes and heat-induced damage.

Alternative In Vitro Methods for the Determination of Viral Capsid Structural Integrity

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Cited by 6 •

2017

Routine detection methods utilizing viral genome amplification are limited by their inability to discriminate infectious from non-infectious particles. The purpose of this article is to provide detailed protocols for alternative methods to aid in discrimination of infectious norovirus particles using aptamer binding, dynamic light scattering, and transmission electron microscopy.

In Vitro Disassembly of Influenza A Virus Capsids by Gradient Centrifugation

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Cited by 4 •

2016

Disassembly of influenza A virus cores during virus entry into host cells is a multistep process. We describe an in vitro method to analyze the early stages of viral uncoating. In this approach, velocity gradient centrifugation is used to biochemically dissect the steps that initiate uncoating under defined conditions.

Helical Organization of Blood Coagulation Factor VIII on Lipid Nanotubes

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Cited by 9 •

2014

We present a combination of Cryo-electron microscopy, lipid nanotechnology, and structure analysis applied to resolve the membrane-bound structure of two highly homologous FVIII forms: human and porcine. The methodology developed in our laboratory to helically organize the two functional recombinant FVIII forms on negatively charged lipid nanotubes (LNT) is described.

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