The Role of Force-Sensitive Interactions in Amyloid Assembly by Fungal Adhesins
type: CreativeWork
description: Candida albicans is a common human fungal pathogen that forms stubborn biofilms on host tissues and implanted cosmetic and medical devices such as contact lenses, dentures, catheters, and joint prostheses. These biofilms assemble through cooperative cell-to-cell attachments using surface-localized adhesin proteins. Some adhesins also help maintain biofilm integrity by forming fibrous protein aggregates that are linked together by non-covalent bonds between a hydrophobic segment of their sequence, termed the amyloid-forming region (AFR). At the core of these adhesin aggregates are parallel or anti-parallel β-sheet arrays, which can layer onto other adhesin β-sheets by sidechain–sidechain interactions to form highly stable amyloid fibrils. The Als (agglutinin-like sequence) proteins are one type of the amyloid fibril-forming adhesin that decorates the cell wall of C. albicans and have been implicated in pathogenesis and biofilm formation. Though some efforts have succeeded in modeling the structures of Als adhesins before and after amyloid formation, little is known about the mechanism of this structural transition. It appears that their AFR is concealed by the bordering N-terminal and T domains prior to amyloid assembly, and shear force-induced partial unfolding of the Als protein is required to expose its AFR, allowing amyloid formation to proceed. We investigated this putative mechanism by examining the relationship between the stability of AFR-concealing intramolecular interactions in the Als5 adhesin and the amount of shear force needed to trigger amyloid formation. Our approach involved developing a surrogate cell system to host and test this relationship for individual Als proteins that had been site-specifically altered to either restrict or facilitate exposure of their AFR under varying levels of shear force. These studies helped identify a shear force-responsive bond near the AFR that appears to aid in AFR concealment.
abstract: Candida albicans is a common human fungal pathogen that forms stubborn biofilms on host tissues and implanted cosmetic and medical devices such as contact lenses, dentures, catheters, and joint prostheses. These biofilms assemble through cooperative cell-to-cell attachments using surface-localized adhesin proteins. Some adhesins also help maintain biofilm integrity by forming fibrous protein aggregates that are linked together by non-covalent bonds between a hydrophobic segment of their sequence, termed the amyloid-forming region (AFR). At the core of these adhesin aggregates are parallel or anti-parallel β-sheet arrays, which can layer onto other adhesin β-sheets by sidechain–sidechain interactions to form highly stable amyloid fibrils. The Als (agglutinin-like sequence) proteins are one type of the amyloid fibril-forming adhesin that decorates the cell wall of C. albicans and have been implicated in pathogenesis and biofilm formation. Though some efforts have succeeded in modeling the structures of Als adhesins before and after amyloid formation, little is known about the mechanism of this structural transition. It appears that their AFR is concealed by the bordering N-terminal and T domains prior to amyloid assembly, and shear force-induced partial unfolding of the Als protein is required to expose its AFR, allowing amyloid formation to proceed. We investigated this putative mechanism by examining the relationship between the stability of AFR-concealing intramolecular interactions in the Als5 adhesin and the amount of shear force needed to trigger amyloid formation. Our approach involved developing a surrogate cell system to host and test this relationship for individual Als proteins that had been site-specifically altered to either restrict or facilitate exposure of their AFR under varying levels of shear force. These studies helped identify a shear force-responsive bond near the AFR that appears to aid in AFR concealment.
author: Petkovic, Andrea
language: eng
keywords: Adhesin, Fungal Adhesin, Candida albicans, Als adhesin, Force-sensitive, Amyloid, Biofilm
license: http://creativecommons.org/licenses/by-nc-nd/4.0/
date published: 2025-01-30
date modified: 2026-07-27T20:35:45Z
provider: Queens University
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: Queens University

PropertyValue
property ID: Handle
value: https://hdl.handle.net/1974/34308