Department of Pharmacology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Buchmann Institute for Molecular Life Sciences and Institute of Biophysical Chemistry, Goethe University, Max-von-Laue-Strasse 15, 60438 Frankfurt, Germany.
Neuron. 2019 Mar 6;101(5):863-875.e6. doi: 10.1016/j.neuron.2019.01.002. Epub 2019 Jan 28.
Regulated secretion is critical for diverse biological processes ranging from immune and endocrine signaling to synaptic transmission. Botulinum and tetanus neurotoxins, which specifically proteolyze vesicle fusion proteins involved in regulated secretion, have been widely used as experimental tools to block these processes. Genetic expression of these toxins in the nervous system has been a powerful approach for disrupting neurotransmitter release within defined circuitry, but their current utility in the brain and elsewhere remains limited by lack of spatial and temporal control. Here we engineered botulinum neurotoxin B so that it can be activated with blue light. We demonstrate the utility of this approach for inducibly disrupting excitatory neurotransmission, providing a first-in-class optogenetic tool for persistent, light-triggered synaptic inhibition. In addition to blocking neurotransmitter release, this approach will have broad utility for conditionally disrupting regulated secretion of diverse bioactive molecules, including neuropeptides, neuromodulators, hormones, and immune molecules. VIDEO ABSTRACT.
受调控的分泌作用对于从免疫和内分泌信号到突触传递等各种生物过程至关重要。肉毒杆菌和破伤风神经毒素特异性地蛋白水解参与受调控的分泌的囊泡融合蛋白,已被广泛用作阻断这些过程的实验工具。这些毒素在神经系统中的遗传表达一直是破坏特定回路中神经递质释放的有力方法,但由于缺乏空间和时间控制,它们在大脑和其他部位的应用仍然受到限制。在这里,我们设计了可以用蓝光激活的肉毒杆菌神经毒素 B。我们证明了这种方法在诱导性破坏兴奋性神经传递中的效用,为持续的、光触发的突触抑制提供了第一个光遗传学工具。除了阻断神经递质释放外,这种方法还将广泛用于条件性破坏各种生物活性分子的受调控分泌,包括神经肽、神经调节剂、激素和免疫分子。视频摘要。