打开APP

Protein synthesis: a high fidelity molecuLAr event

Rachel Green (Johns Hopkins U., HHMI) 1: Protein synthesis: a high fidelity molecuLAr event

Talk Overview:
In her first talk, Green provides a detailed look at protein synthesis, or transLAtion. TransLAtion is the process by which nucleotides, the “LAnguage” of DNA and RNA, are transLAted into amino acids, the “LAnguage” of proteins. Green begins by describing the components needed for transLAtion; mRNA, tRNA, ribosomes, and the initiation, elongation, and termination factors. She then expLAins the roles of these pLAyers in ensuring accuracy during the initiation, elongation, termination and recycling steps of the transLAtion process. By comparing transLAtion in bacteria and eukaryotes, Green expLAins that it is possible to determine which components and steps are highly conserved and predate the divergence of different kingdoms on the tree of life, and which are more recent adaptations.
Green’s second talk focuses on work from her LAb investigating how ribosomes detect defective mRNAs and trigger events leading to the degradation of the bad RNA and the incompletely transLAted protein product and to the recycling of the ribosome components. Working in yeast and using a number of biochemical and genetic techniques, Green’s LAb showed that the protein Dom34 is critical for facilitating ribosome release from the short mRNAs that result from mRNA cleavage. Experiments showed that Dom34-mediated rescue of ribosomes from short mRNAs is an essential process for cell survival in higher eukaryotes.

Speaker Biography:
Rachel Green received her BS in chemistry from the University of Michigan. She then moved to Harvard to pursue her PhD in the LAb of Jack Szostak where she worked on designing catalytic RNA molecules and investigating their implications for the evolution of life. As a post-doctoral fellow at the University of California, Santa Cruz, Green began to study how the ribosome transLAtes mRNA to protein with such accuracy.

Currently, Green is a Professor of MolecuLAr Biology and Genetics at the Johns Hopkins School of Medicine and an Investigator of the Howard Hughes Medical Institute. Research in her LAb continues to focus on the ribosome and factors involved in the fidelity of eukaryotic and prokaryotic transLAtion.

Green is the recipient of a Johns Hopkins University School of Medicine Graduate Teaching Award as well as the recipient for numerous awards for her research. She was elected to the National Academy of Sciences in 2012.

2016-04-28 课时:44分钟

Protein synthesis: mRNA surveilLAnce by the ribosome

Rachel Green (Johns Hopkins U., HHMI) 2: Protein synthesis: mRNA surveilLAnce by the ribosome

Talk Overview:
In her first talk, Green provides a detailed look at protein synthesis, or transLAtion. TransLAtion is the process by which nucleotides, the “LAnguage” of DNA and RNA, are transLAted into amino acids, the “LAnguage” of proteins. Green begins by describing the components needed for transLAtion; mRNA, tRNA, ribosomes, and the initiation, elongation, and termination factors. She then expLAins the roles of these pLAyers in ensuring accuracy during the initiation, elongation, termination and recycling steps of the transLAtion process. By comparing transLAtion in bacteria and eukaryotes, Green expLAins that it is possible to determine which components and steps are highly conserved and predate the divergence of different kingdoms on the tree of life, and which are more recent adaptations.
Green’s second talk focuses on work from her LAb investigating how ribosomes detect defective mRNAs and trigger events leading to the degradation of the bad RNA and the incompletely transLAted protein product and to the recycling of the ribosome components. Working in yeast and using a number of biochemical and genetic techniques, Green’s LAb showed that the protein Dom34 is critical for facilitating ribosome release from the short mRNAs that result from mRNA cleavage. Experiments showed that Dom34-mediated rescue of ribosomes from short mRNAs is an essential process for cell survival in higher eukaryotes.

Speaker Biography:
Rachel Green received her BS in chemistry from the University of Michigan. She then moved to Harvard to pursue her PhD in the LAb of Jack Szostak where she worked on designing catalytic RNA molecules and investigating their implications for the evolution of life. As a post-doctoral fellow at the University of California, Santa Cruz, Green began to study how the ribosome transLAtes mRNA to protein with such accuracy.

Currently, Green is a Professor of MolecuLAr Biology and Genetics at the Johns Hopkins School of Medicine and an Investigator of the Howard Hughes Medical Institute. Research in her LAb continues to focus on the ribosome and factors involved in the fidelity of eukaryotic and prokaryotic transLAtion.

Green is the recipient of a Johns Hopkins University School of Medicine Graduate Teaching Award as well as the recipient for numerous awards for her research. She was elected to the National Academy of Sciences in 2012.

2016-04-28 课时:38分钟

Introducing the EnSight™ Multimode PLAte Reader from PerkinElmer

PerkinElmer's EnSight Multimode PLAte Reader is the first benchtop system to offer well-imaging alongside LAbel-free and LAbeled detection technologies - for a whole new perspective on your research. For more information, please visit the EnSight website - http://bit.ly/T4IDPh

2016-06-02 课时:4分钟

Inermediate FiLAments中间丝

中间丝的基本构建块是二聚体,它在细胞质和细胞核中形成复杂的网络,它是灵活的,可扩展的,很难打破的,在活细胞中有动态的性质,它的拆卸和组装是受激酶和磷酸酶参与信号转导。西北大学费因伯格医学和海洋生物学院的鲍勃戈德曼从中间丝的命名到中间丝蛋白家族,为我们讲解细胞骨架中间丝的作用及细胞骨架的相互对话与稳定性、细胞的机械完整性、细胞形状的测定与维护; 波形蛋白迅速诱导上皮细胞改变形状,增加上皮细胞的活力......

2016-07-25 课时:37分钟

MolecuLAr Chaperones in the Eukayotic Cell

为什么组织特异性?为什么这些有毒蛋白质?为什么不协在神经元的反应?为什么伴侣不是百分之.......霍华德休斯医学研究所Art Horwich在真核细胞中的伴侣蛋白分子的讲座中将一一为您解答。

2016-07-26 课时:21分钟

NeuromuscuLAr Connectomics

Part 2:使用不同颜色的转基因小鼠, 荧光标记的蛋白质在每个神经元(“彩虹”老鼠), Lichtman和他的同事们能够遵循的形成, 在小鼠发育过程中的神经肌肉接头的破坏。这项工作是2部分的重点。

2016-07-29 课时:39分钟

MolecuLAr Architecture of the Circadian Clock in Mannals

在这个讲座中,Takahashi介绍了如何穿越不同遗传B许多老鼠背景允许他的实验室识别几个基因通过不同的机制影响时钟基因系统的输出。与晶体结构Takahashi开始他的演讲的最后一部分的Bmal和时钟,时钟基因的转录激活因子的两个中心。他继续描述他的实验室展示的是怎样的Bmal /时钟控件的转录调控的DNA结合活性调节不仅循环基因,而且基本的细胞功能如RNA聚合酶2占用和组蛋白修饰。

2016-08-04 课时:35分钟

Rescuing US bIomedical Research From Its Systemic FLAws

这些在生物医学研究领域的领导者已经把他们的注意力转向问题这是面临的实践和可持续发展的基础研究美国的企业。他们的关切和想法应对这些挑战已发表在诉讼程序中的美国国家科学院(2014年4月22日)。在谈话中,Alberts,Kirschner,蒂尔曼和斯讨论本文的成因,需要关注的核心问题,以及需要涉及更大的科学社区在保障活力的过程中生物医学研究企业。

2016-09-26 课时:13分钟

CytopLAsm是什么?

Margaret Gardel探讨细胞质的物理性质,一个复杂的流体内的细胞,是挤满了蛋白质,细胞器和丝状网络。她沉思,例如,运动蛋白如何克服身体携带的货物的阻力,以及如何细胞进行形状的变化,以应对不同的刺激。为了帮助解决这些问题,她提出了一个“新物理学”。

2016-11-16 课时:12分钟

看得见的蛋白互作-Duolink PLA实验操作视频

Duolink® 实验基于邻位连接技术(Proximity Ligation Assay, PLA),可将蛋白信号放大1000倍,实现单分子级别检测灵敏度。即使是微量样本、微弱互作、极罕见低丰度表达,也能在细胞生理水平下,获得基于图像的可视化蛋白检测结果,真实反映内源表达水平蛋白的互作、定位和定量,结果可靠有说服力。该视频详细介绍了Duolink实验的每步操作,请跟随Tracy Adair-Kirk博士,一起开启Duolink® PLA®实验之旅。

2018-01-31 课时:5分钟