摘要
By coupling in situ [ 2+ 3] Huisgen cycloaddition with an in vitro transcription/ translation luminescence assay in a crude ribosomal extract, a robust and accurate high- throughput platform was successfully developed and applied for efficient identification of novel structural types of ribosomal inhibitors with antimicrobial activity against drug- resistant bacteria.
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单位四川省医学科学院(四川省人民医院); 电子科技大学; 四川大学; 成都中医药大学