Related Experiment Video
Updated: Feb 9, 2026

Detection of Abnormal Prion Protein by Immunohistochemistry
Published on: May 5, 2023
Addressing Intracellular Amyloidosis in Bacteria with RepA-WH1, a Prion-Like Protein
Laura Molina-García1,2, Fátima Gasset-Rosa1,3, María Moreno-Del Álamo1,4
1Department of Cellular and Molecular Biology, Centro de Investigaciones Biológicas (CSIC), Madrid, Spain.
Abstract:
Bacteria are the simplest cellular model in which amyloidosis has been addressed. It is well documented that bacterial consortia (biofilms) assemble their extracellular matrix on an amyloid scaffold, yet very few intracellular amyloids are known in bacteria. Here, we describe the methods we have resorted to characterize in Escherichia coli cells the amyloidogenesis, propagation, and dynamics of the RepA-WH1 prionoid. This prion-like protein, a manifold domain from the plasmid replication protein RepA, itself capable of assembling a functional amyloid, causes when expressed in E. coli a synthetic amyloid proteinopathy, the first model for an amyloid disease with a purely bacterial origin. These protocols are useful to study other intracellular amyloids in bacteria.
Related Concept Videos
Intracellular Movement of Viruses and Bacteria
Cytoskeletal Proteins in Bacteria
Strategies for Assessing and Addressing Confounding
Confounding can be addressed at both the design phase of a study and through analytical methods after data...
Intracellular Signaling Cascades
Intracellular Hormone Receptors
The Roles of Bacteria and Fungi in Plant Nutrition

