INTRINSIC PROBES OF SMOOTH MUSCLE MYOSIN DYNAMICS

这一建议的最终目标是研究Smooth中特定位置的构象变化 肌肉肌球蛋白使用内源性色氨酸荧光。平滑肌肌球蛋白的构建将从基因上 被设计成在所需的感兴趣的部位含有单个色氨酸或一对色氨酸，这 将提供独特的内在荧光信号，报告局部构象和结构的变化 对核苷酸结合、三磷酸腺苷水解、肌动蛋白结合和杠杆臂运动的反应。这些实验 是对该领域正在进行的结构研究的补充，使我们能够明确地测试预测 关于收缩周期中关键步骤中的结构域移动和结构重排 肌肉肌球蛋白。因此，我们将能够将肌球蛋白的结构变化与功能后果联系起来， 与某些心血管疾病直接相关。例如，FHC(家族性肥厚性 心肌病)是一种遗传性疾病，通常是致命的，由 肌球蛋白对其作为分子马达的正常功能至关重要。我们将研究结构变化在 直接受FHC基因突变影响的分子区域的肌球蛋白。这将导致一个更好的 了解这种疾病，从而更好地选择治疗方法。因此，这项建议提供了一个 批判性地测试有关肌肉分子机制的基本问题的独特机会 以前通过其他光谱探针研究无法获得的收缩，以及结果 将对FHC等严重疾病州产生重要影响。

The ultimate goal of this proposal is to examine conformational changes at specific locations within smooth muscle myosin using intrinsic tryptophan fluorescence. Smooth muscle myosin constructs will be genetically engineered to contain either a single tryptophan or a pair of tryptophans at the desired site of interest, which will provide a unique intrinsic fluorescence signal reporting local conformational and structural changes in response to nucleotide binding, ATP hydrolysis, actin-binding, and lever arm movement. These experiments are complementary to the ongoing structural studies in the field, allowing us to explicitly test predictions about domain movements and structural rearrangements during critical steps in the contractile cycle smooth muscle myosin. Thus we will be able to correlate structural changes in myosin with functional consequences, which relates directly to certain cardiovascular disease. For example, FHC (familial hypertrophic cardiomyopathy) is an inherited, often lethal disease caused by point mutations at key structures within myosin critical to its proper functioning as a molecular motor. We will be examining structural changes in myosin in regions of the molecule directly impacted by mutations that underlie FHC. This will lead to a better understanding of the disease, and thus to better treatment options as well. Therefore, this proposal offers a unique opportunity to critically test fundamental questions about the molecular mechanism of muscle contraction that have not been previously accessible by other spectroscopic probe studies, and the results will have important implications for serious disease states such as FHC.