Authors
Aakhya Rastogi, Pragati Vishwakarma, Chia-Yu Chang, Chia-Ching Chang, Tapan Kumar Chaudhuri
Published in
Progress in biophysics and molecular biology. Pages 101946. Aug 20, 2026. Epub Aug 20, 2026.
Abstract
Viral capsid organization represents a controlled physical self-assembly process in biology. Bacteriophage MS2 has a well-characterized coat protein and a simple RNA-protein interaction network, making it a prime system for studying how physical factors such as geometry, energy, and RNA arrangement influence capsid assembly, flexibility, and function. This review integrates literature on structure, energy, and RNA organization to examine MS2 capsid architecture. It suggests that the capsid's structure arises from a physical landscape rather than a fixed assembly process. We explore conformational diversity, quasi-equivalence (in which identical subunits adopt different but energetically comparable structures), and structural polymorphism inherent in this model. We also emphasize upon RNA's active role in organization, rather than its passive cargo role. Furthermore, we argue that the physical principles underlying capsid assembly are key to the use of MS2 virus-like particles in drug delivery, vaccines, imaging, and nanotechnology. These applications leverage the same constraints that otherwise shape native structures, converting them into useful biomedical tools. The review highlights ongoing questions at the crossroads of virology, structural biology, and VLP engineering, to develop predictive models that accurately forecast assembly outcomes across diverse capsid architectures.
PMID:
42624377
Bibliographic data and abstract were imported from PubMed on 21 Aug 2026.
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