Champney Scott
Department of Biomedical Sciences, JH Quillen Collage of Medicine, East Tennessee State University, Johnson City, TN 37614, USA.
Antibiotics (Basel). 2022 Jul 13;11(7):937. doi: 10.3390/antibiotics11070937.
This review discusses the inhibition of macromolecular structure formation as a novel and under-investigated drug target. The disruption of cell wall structures by penicillin-binding protein interactions is one potential target. Inhibition of DNA polymerase III assembly by novel drugs is a second target that should be investigated. RNA polymerase protein structural interactions are a third potential target. Finally, disruption of ribosomal subunit biogenesis represents a fourth important target that can be further investigated. Methods to examine these possibilities are discussed.
本综述讨论了抑制大分子结构形成作为一个新的且研究不足的药物靶点。通过青霉素结合蛋白相互作用破坏细胞壁结构是一个潜在靶点。新型药物抑制DNA聚合酶III组装是第二个应研究的靶点。RNA聚合酶蛋白结构相互作用是第三个潜在靶点。最后,破坏核糖体亚基生物合成是第四个可进一步研究的重要靶点。文中讨论了检验这些可能性的方法。