Halda Therapeutics

None Gina Vitale
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Abstract

Craig Crews is no stranger to the challenge of devising a punchy name for a new class of drug. The chemical biologist was involved in both the discovery and the naming of proteolysis-targeting chimeras, or PROTACs, which are double-ended molecules that degrade proteins. When Crews founded Halda Therapeutics to develop another new class of drug, he and the leadership team—including Executive Chair Tim Shannon and Chief Scientific Officer Kat Kayser-Bricker—wanted to give these molecules a moniker that’s a little graver. “We wanted to kill cells,” Crews says. “We had to figure out a way to make sure that RIP found its way into the name.” And so regulated induced proximity targeting chimeras, or RIPTACs, were christened. As the moniker suggests, a double-ended RIPTAC brings two proteins together. With one end, it binds a protein that is overexpressed in a tumor, which helps the RIPTAC get to, and stay inside, the
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Halda疗法
克雷格·克鲁斯(Craig Crews)对为一类新毒品想出一个有力的名字并不陌生。这位化学生物学家参与了蛋白水解靶向嵌合体(PROTACs)的发现和命名,这是一种降解蛋白质的双端分子。当克鲁斯成立哈尔达治疗公司开发另一类新药时,他和领导团队——包括执行主席蒂姆·香农和首席科学官凯特·凯瑟-布里克——想给这些分子起一个更严肃的名字。“我们想杀死细胞,”克鲁斯说。“我们必须找到一种方法,确保RIP在名字中找到了一席之地。”因此,调控诱导近距离靶向嵌合体(简称riptac)被命名。顾名思义,双端RIPTAC将两种蛋白质结合在一起。它的一端与肿瘤中过度表达的蛋白质结合,帮助RIPTAC进入并留在肿瘤内部
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