Structural and Mechanical Characterization of Viruses with AFM

Methods Mol Biol. 2019:1886:259-278. doi: 10.1007/978-1-4939-8894-5_15.

Abstract

Microscopes are used to characterize small objects with the help of probes that interact with the specimen, such as photons and electrons in optical and electron microscopies, respectively. In atomic force microscopy (AFM) the probe is a nanometric tip located at the end of a micro cantilever which palpates the specimen under study as a blind person manages a walking stick. In this way AFM allows obtaining nanometric resolution images of individual protein shells, such as viruses, in liquid milieu. Beyond imaging, AFM also enables not only the manipulation of single protein cages, but also the characterization of every physicochemical property able of inducing any measurable mechanical perturbation to the microcantilever that holds the tip. In this chapter we start revising some recipes for adsorbing protein shells on surfaces. Then we describe several AFM approaches to study individual protein cages, ranging from imaging to spectroscopic methodologies devoted for extracting physical information, such as mechanical and electrostatic properties. We also explain how a convenient combination of AFM and fluorescence methodologies entails monitoring genome release from individual viral shells during mechanical unpacking.

Keywords: Aqueous solution; Atomic force microscopy; Beam deflection; Breaking; Cantilever; Disruption; Electrostatics; Fatigue; Force curve; Nanoindentation; Stylus; Tip; Topography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Capsid
  • Data Analysis
  • Humans
  • Image Processing, Computer-Assisted / methods
  • Mechanical Phenomena
  • Microscopy, Atomic Force* / methods
  • Static Electricity
  • Viral Proteins / chemistry
  • Viruses / ultrastructure*

Substances

  • Viral Proteins