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DESCRIPTION (provided by applicant): We request funds for the purchase of an FEI Tecnai G2 Spirit BioTwin transmission electron microscope (TEM) with embedded CCD camera. This will serve the biomedical research needs of eleven NIH-funded investigators at the University of Massachusetts Medical School (UMMS) and Boston University School of Medicine. The microscope will be housed in the Core EM Facility of UMMS, and maintained and monitored by the Facility Manager, ensuring efficient use by investigators. It will replace a 23-year old, second-hand Philips CM12, which is based on outdated technology, lacks key capabilities required by users, and for which maintenance is likely to be discontinued or become difficult in the near future. The new instrument would immediately solve these problems. The projects that will use the Tecnai include fundamental studies of autophagic and apoptotic cell death, mechanisms of synapse formation, the regulation of contraction in smooth and striated muscle, the role of MAP kinase signaling pathways in neurodegeneration, the function of centrosomes in normal and diseased cells, the regulation of G-protein-coupled receptors, the structure and function of spliceosomes, and the structure and function of cilia and flagella in normal and diseased states. These projects require TEM as an essential tool for investigating cellular and molecular architecture at high resolution and as a means of detecting and localizing specific cell molecules by immuno-gold labeling. The images obtained will provide essential insights into mechanisms of cell development, function, infection and disease. In addition to the users in this application, there are numerous other investigators at UMMS who use TEM on a more occasional basis and who would also benefit from modernization of our TEM technology. The instrument proposed represents the state-of-the-art for a conventional TEM, and has many features that would greatly enhance TEM productivity at UMMS. These include a modern, user-friendly computer interface, motorized stage controls with 180o tilt capability, the ability to store and recall grid locations and alignment and imaging parameters (especially useful in several studies requiring serial sectioning), and full integration of an embedded CCD camera, making it possible to record images rapidly and with full documentation. All of the projects that will use the microscope aim to provide fundamental insights into cellular structure and function. Most have a direct bearing on the understanding of human disease. Access to this state-of-the-art instrument will play a key role in advancing our knowledge in these biomedically important areas.
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DOI: 10.1101/gad.305888.117
发表时间: 2017-10-15
期刊: Genes & development
影响因子: 10.5
作者: [Coutinho-Budd JC, Sheehan AE, Freeman MR]
通讯作者: Freeman MR
DOI: 10.1016/j.neuron.2014.06.026
发表时间: 2014-07-16
期刊: NEURON
影响因子: 16.2
作者: [Stork, Tobias, Sheehan, Amy, Tasdemir-Yilmaz, Ozge E., Freeman, Marc R.]
通讯作者: Freeman, Marc R.
Astrocytes engage unique molecular programs to engulf pruned neuronal debris from distinct subsets of neurons.
星形胶质细胞涉及独特的分子程序,以吞噬不同神经元子集的修剪修剪的神经元碎片。
DOI: 10.1101/gad.229518.113
发表时间: 2014-01-01
期刊: Genes & development
影响因子: 10.5
作者: [Tasdemir-Yilmaz OE, Freeman MR]
通讯作者: Freeman MR
Robust Distal Tip Cell Pathfinding in the Face of Temperature Stress Is Ensured by Two Conserved microRNAS in Caenorhabditis elegans.
秀丽隐杆线虫中的两个保守的microRNA确保了在温度应力下的良好远端尖端细胞途径。
DOI: 10.1534/genetics.115.179184
发表时间: 2015-08
期刊: Genetics
影响因子: 3.3
作者: [Burke SL, Hammell M, Ambros V]
通讯作者: Ambros V
8
    Mechanism of regulation of cardiac contraction by phosphorylation of myosin binding protein C
    • 批准号:
      10223413
    • 项目类别:
    • 资助金额:
      $68.04万
    • 财政年份:
      2018
    • 负责人:
      ROGER W CRAIG
    • 依托单位:
    Structure of The Interacting-Heads Motif in Myosin Filaments and Molecules
    Structure of The Interacting-Heads Motif in Myosin Filaments and Molecules
    Skeletal myosin-binding protein C (MyBP-C): molecular structure and function
    海外基金