A new combinatorial approach for the biosynthesis and screening of small drug-like toxin inhibitors inside living cells is presented. This approach has been initially used as proof of principle for finding inhibitors against the LF factor from Bacillus anthracis. Key to our ''living combinatorial'' approach is the use of a living cell as a micro-chemical factory for both synthesis and screening of potential inhibitors for a given molecular recognition event (see Scheme 1). This powerful technique posses the advantage that both processes synthesis and screening happen inside the cell thus accelerating the whole screening/selection process
The number of newly approved antimicrobial compounds has been steadily decreasing over the past 50 y...
Although combinatorial libraries owe their inception to applications in peptide and bacteriophage li...
Mixture based synthetic combinatorial libraries offer a tremendous enhancement for the rate of drug ...
Available methods for developing and screening small drug-like molecules able to knockout toxins or ...
Combinatorial chemistry has become an important aspect of medicinal research due to its flexibility ...
Several combinatorial methods have been developed to create focused or diverse chemical libraries wi...
AbstractBackground: The rapidly expanding list of pharmacologically important targets has highlighte...
Ligands based on bicyclic peptides can combine favourable properties of antibodies (good binding aff...
Combinatorial screening methodology has been employed to select new affinity specific ligands to bil...
AbstractBackground: The increasing interest in combinatorial chemistry as a tool for the development...
Antibiotic resistance has been a developing problem for mankind in recent decades and multi-drug res...
A previously developed method for cyclic peptide synthesis was demonstrated to be able to provide co...
Combinatorial methods of chemical synthesis allow the creation of molecular libraries having immense...
Chemical probes that label proteins of interest in the context of complex biological samples are use...
The number of newly approved antimicrobial compounds has been steadily decreasing over the past 50 y...
The number of newly approved antimicrobial compounds has been steadily decreasing over the past 50 y...
Although combinatorial libraries owe their inception to applications in peptide and bacteriophage li...
Mixture based synthetic combinatorial libraries offer a tremendous enhancement for the rate of drug ...
Available methods for developing and screening small drug-like molecules able to knockout toxins or ...
Combinatorial chemistry has become an important aspect of medicinal research due to its flexibility ...
Several combinatorial methods have been developed to create focused or diverse chemical libraries wi...
AbstractBackground: The rapidly expanding list of pharmacologically important targets has highlighte...
Ligands based on bicyclic peptides can combine favourable properties of antibodies (good binding aff...
Combinatorial screening methodology has been employed to select new affinity specific ligands to bil...
AbstractBackground: The increasing interest in combinatorial chemistry as a tool for the development...
Antibiotic resistance has been a developing problem for mankind in recent decades and multi-drug res...
A previously developed method for cyclic peptide synthesis was demonstrated to be able to provide co...
Combinatorial methods of chemical synthesis allow the creation of molecular libraries having immense...
Chemical probes that label proteins of interest in the context of complex biological samples are use...
The number of newly approved antimicrobial compounds has been steadily decreasing over the past 50 y...
The number of newly approved antimicrobial compounds has been steadily decreasing over the past 50 y...
Although combinatorial libraries owe their inception to applications in peptide and bacteriophage li...
Mixture based synthetic combinatorial libraries offer a tremendous enhancement for the rate of drug ...