Anti-infective drug discovery is a multifaceted endeavor aimed at identifying and developing compounds capable of combating microbial infections. This process involves a myriad of scientific disciplines, from molecular biology and pharmacology to chemistry and computational modeling. At its core, the goal of anti-infective drug discovery is to devise novel therapeutics that effectively target pathogens while minimizing adverse effects on the host.
Researchers begin by identifying potential drug targets within pathogens, such as bacteria, viruses, fungi, and parasites. These targets may be essential proteins, enzymes, or other molecules critical for the pathogen's survival or replication. Utilizing advanced techniques like genomics, proteomics, and bioinformatics, scientists analyze the molecular pathways and mechanisms involved in infection, pinpointing vulnerabilities that can be exploited for therapeutic intervention.
Once potential targets are identified, the next step is to screen large libraries of chemical compounds for molecules that interact with these targets. High-throughput screening assays enable researchers to rapidly test thousands or even millions of compounds for their ability to inhibit pathogen growth or disrupt essential processes. This initial screening phase identifies lead compounds with promising anti-infective activity.
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Thomas J Webster, Brown University, United States
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