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Expression Studies Of Other Unconventional Myosins

Expression Studies Of Other Unconventional Myosins
其他非常规肌球蛋白的表达研究
批准号:
6690568
负责人:
JAMES R. SELLERS
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至

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中文摘要
翻译
我们正在使用杆状病毒/Sf 9系统表达其他几种非传统的肌球蛋白,包括来自鲎(鲎)的肌球蛋白III和来自人类的肌球蛋白XV。肌球蛋白III是不寻常的,因为有一个激酶域的氨基末端。肌球蛋白只存在于视觉系统的感光细胞中。全长克隆在Sf 9细胞中表达良好,并已纯化至均一。有趣的是,在初步实验中,我们无法检测到任何MgATPase活性或肌动蛋白结合。蛋白质以昼夜节律的方式原位磷酸化。我们正在研究这种磷酸化是否对其活性有任何影响。肌球蛋白XV是一种相对较新发现的肌球蛋白,在小鼠和人类中被鉴定为耳聋基因。它有一个很长的富含脯氨酸的氨基末端延伸,功能未知,可以选择性剪接。我们正在尝试表达三个片段:一个包含通过轻链结合基序的氨基末端延伸的片段(长S1),一个删除选择性剪接氨基末端的片段(短S1)和一个全长构建体。到目前为止,只有短的S1似乎以可溶形式表达。我们目前正在评估其酶活性。肌球蛋白IX是一种不寻常的肌球蛋白,其在其尾部含有GT3激活结构域。肌球蛋白是单头的,没有很好的表征。我们已经开始表达这种肌球蛋白的头部片段,但发现这种蛋白质似乎表达得不好。
英文摘要
We are using the baculoviral/Sf9 systems to express several other unconventional myosins, including myosin III from Limulus, the horseshoe crab, and myosin XV from human. Myosin III is unusual in that there is a kinase domain at the amino-terminus. The myosin is found exclusively in the photoreceptor cells of the visual system. A full-length clone expresses well in Sf9 cells and has been purified to homogeneity. Interestingly, we are unable to detect any MgATPase activity or actin binding in preliminary experiments. The protein is phosphorylated in situ in a circadian manner. We are investigating whether this phosphorylation plays any effect on its activity. Myosin XV is a relatively newly discovered myosin that was identified in mice and humans as a deafness gene. It has a very long proline-rich amino-terminal extension of unknown function which can be alternatively spliced. We are attemping to express three fragments: a fragment that contains the amino-terminus extension through the light chain binding motifs (long S1), a fragment that deletes the alternatively-spliced amino-terminus (short S1) and a full-length construct. So far, only the short S1 appears to be expressed in a soluble form. We are currently assessing its enzymatic activity. Myosin IX is an unusual myosin which contains a GTPase activating domain in its tail. The myosin is single-headed and is not well characterized. We have begun the expression of head fragments of this myosin but find that the protein does not appear to express well.
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