Chronic mucoid P. aeruginosa cystic fibrosis (CF) lung infections are associated with the development of a biofilm composed of anionic acetylated exopolysaccharide (EPS) alginate, electrostatically stabilised by extracellular Ca2+ ions. OligoG CF-5/20, a low molecular weight guluronate rich oligomer, is emerging as a novel therapeutic capable of disrupting mature P. aeruginosa biofilms. However, its method of therapeutic action on the mucoid biofilm EPS is not definitively known at a molecular level. This work, utilising molecular dynamics (MD) and Density-Functional Theory (DFT), has revealed that OligoG CF-5/20 interaction with the EPS is facilitated solely through bridging Ca2+ ions, which are not liberated from their native EPS binding ...
Afflicting more than 700,000 people worldwide, Cystic Fibrosis (CF) is a disorder characterized by t...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
Cystic fibrosis (CF) is an autosomal recessive, life-limiting condition characterized by progressive...
Mucoid Pseudomonas aeruginosa is a prevalent cystic fibrosis (CF) lung coloniser whose chronicity is...
Acquisition of a mucoid phenotype by Pseudomonas sp. in the lungs of cystic fibrosis (CF) patients, ...
Acquisition of a mucoid phenotype by Pseudomonas sp. in the lungs of cystic fibrosis (CF) patients, ...
Mucoid Pseudomonas aeruginosa is a prevalent cystic fibrosis (CF) lung colonizer, producing an extra...
Bacterial and fungal biofilms are an increasing clinical challenge, from non-healing wounds to chron...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
Concerns about acquisition of antibiotic resistance have led to increasing demand for new antimicrob...
Pseudomonas aeruginosa (PA) infections in Cystic Fibrosis (CF) patients are not easily cleared due t...
Biofilms are communities of microbes embedded in a matrix of extracellular polymeric substances, lar...
Afflicting more than 700,000 people worldwide, Cystic Fibrosis (CF) is a disorder characterized by t...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
Cystic fibrosis (CF) is an autosomal recessive, life-limiting condition characterized by progressive...
Mucoid Pseudomonas aeruginosa is a prevalent cystic fibrosis (CF) lung coloniser whose chronicity is...
Acquisition of a mucoid phenotype by Pseudomonas sp. in the lungs of cystic fibrosis (CF) patients, ...
Acquisition of a mucoid phenotype by Pseudomonas sp. in the lungs of cystic fibrosis (CF) patients, ...
Mucoid Pseudomonas aeruginosa is a prevalent cystic fibrosis (CF) lung colonizer, producing an extra...
Bacterial and fungal biofilms are an increasing clinical challenge, from non-healing wounds to chron...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
Concerns about acquisition of antibiotic resistance have led to increasing demand for new antimicrob...
Pseudomonas aeruginosa (PA) infections in Cystic Fibrosis (CF) patients are not easily cleared due t...
Biofilms are communities of microbes embedded in a matrix of extracellular polymeric substances, lar...
Afflicting more than 700,000 people worldwide, Cystic Fibrosis (CF) is a disorder characterized by t...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
Cystic fibrosis (CF) is an autosomal recessive, life-limiting condition characterized by progressive...