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    • 2. 发明授权
    • Method for extracting quantitative information relating to an influence on a cellular response
    • 提取与细胞反应有关的定量信息的方法
    • US08058008B2
    • 2011-11-15
    • US10072036
    • 2002-02-05
    • Ole ThastrupSara Petersen BjørnSoren TullinKasper AlmholtKurt Scudder
    • Ole ThastrupSara Petersen BjørnSoren TullinKasper AlmholtKurt Scudder
    • G01N33/53G01N21/76C12P21/02
    • G01N33/5041G01N33/5005G01N33/5008G01N33/5014G01N33/5035G01N33/533G01N33/582G01N2333/43595G01N2333/9121
    • Cells are genetically modified to express a luminophore, e.g., a modified (F64L, S65T, Y66H) Green Fluorescent Protein (GFP, EGFP) coupled to a component of an intracellular signalling pathway such as a transcription factor, a cGMP- or cAMP-dependent protein kinase, a cyclin-, calmodulin- or phospholipid-dependent or mitogen-activated serine/threonin protein kinase, a tyrosine protein kinase, or a protein phosphatase (e.g. PKA, PKC, Erk, Smad, VASP, actin, p38, Jnk1, PKG, IkappaB, CDK2, Grk5, Zap70, p85, protein-tyrosine phosphatase 1C, Stat5, NFAT, NFkappaB, RhoA, PKB). An influence modulates the intracellular signalling pathway in such a way that the luminophore is being redistributed or translocated with the component in living cells in a manner experimentally determined to be correlated to the degree of the influence. Measurement of redistribution is performed by recording of light intensity, fluorescence lifetime, polarization, wavelength shift, resonance energy transfer, or other properties by an apparatus consisting of e.g. a fluorescence microscope and a CCD camera. Data stored as digital images are processed to numbers representing the degree of redistribution. The method can be used as a screening program for identifying a compound that modulates a component and is capable of treating a disease related to the function of the component.
    • 细胞被遗传修饰以表达发光体,例如,与细胞内信号传导途径的组分偶联的经修饰的(F64L,S65T,Y66H)绿色荧光蛋白(GFP,EGFP),例如转录因子,cGMP-或cAMP依赖性 蛋白激酶,细胞周期蛋白,钙调蛋白或磷脂依赖性或丝裂原活化的丝氨酸/苏氨酸蛋白激酶,酪氨酸蛋白激酶或蛋白磷酸酶(例如PKA,PKC,Erk,Smad,VASP,肌动蛋白,p38,Jnk1, PKG,IkappaB,CDK2,Grk5,Zap70,p85,蛋白质 - 酪氨酸磷酸酶1C,Stat5,NFAT,NFkappaB,RhoA,PKB)。 影响调节细胞内信号传导途径,使得发光体在活体细胞中以组分重新分配或移位,其方式通过实验确定与影响程度相关。 重新分布的测量是通过记录光强度,荧光寿命,极化,波长偏移,共振能量转移或其它性质通过由例如, 荧光显微镜和CCD相机。 作为数字图像存储的数据被处理成表示再分配程度的数字。 该方法可以用作鉴定调节成分并能够治疗与该成分的功能有关的疾病的化合物的筛选程序。
    • 3. 发明授权
    • Method for extracting quantitative information relating to an influence on a cellular response
    • 提取与细胞反应有关的定量信息的方法
    • US06518021B1
    • 2003-02-11
    • US09417197
    • 1999-10-07
    • Ole ThastrupSara Petersen BjørnSoren TullinKasper AlmholtKurt Scudder
    • Ole ThastrupSara Petersen BjørnSoren TullinKasper AlmholtKurt Scudder
    • C12Q168
    • G01N33/5041G01N33/5005G01N33/5008G01N33/5014G01N33/5035G01N33/533G01N33/582G01N2333/43595G01N2333/9121
    • Cells are genetically modified to express a luminophore, e.g., a modified (F64L, S65T, Y66H) Green Flourescent Protein (GFP, EGFP) coupled to a component of an intracellular signalling pathway such as a transcription factor, a cGMP- or cAMP-dependent protein kinase, a cyclin-, calmodulin- or phospholipid-dependent or mitogen-activated serine/threonin protein kinase, a tryosine protein kinase, or a protein phosphatase (e.g. PKA, PKC, Erk, Smad, VASP, actin, p38, Jnkl, PKG, IkappaB, CDK2, Grk5, Zap70, p85, protein-tyrosine phosphatase 1C, Stat5, NFAT, NFkappaB, RhoA, PKB). An influence modulates the intracellular signaling pathway in such a way that the luminophore is being redistributed or translocated with the component in living cells in a manner experimentally determined to be correlated to the degree of influence. Measurement of redistribution is performed by recording of light intensity, flourescence lifetime, polarization, wavelength shift, resonance energy transfer, or other properties by an apparatus consisting of e.g. a flourescence microscope and a CCD camera. Data stored as digital images are processed to numbers representing the degree of redistribution. The method can be used as a screening program for identifying a compound that modulates a component and is capable of treating a disease related to the function of the component.
    • 细胞被遗传修饰以表达发光体,例如,与细胞内信号传导途径的组分偶联的经修饰的(F64L,S65T,Y66H)绿色荧光蛋白(GFP,EGFP),例如转录因子,cGMP-或cAMP依赖性 蛋白激酶,细胞周期蛋白,钙调蛋白或磷脂依赖性或丝裂原活化丝氨酸/苏氨酸蛋白激酶,软骨蛋白激酶或蛋白磷酸酶(例如PKA,PKC,Erk,Smad,VASP,肌动蛋白,p38,Jnk1, PKG,IkappaB,CDK2,Grk5,Zap70,p85,蛋白质 - 酪氨酸磷酸酶1C,Stat5,NFAT,NFkappaB,RhoA,PKB)。 影响调节细胞内信号传导途径,使发光体以活体细胞中的成分重新分配或易位,其方式通过实验确定与影响程度相关。 重新分布的测量是通过记录光强度,荧光寿命,极化,波长偏移,共振能量转移或其它性质通过由例如包含的装置组成的装置进行的。 荧光显微镜和CCD相机。 作为数字图像存储的数据被处理成表示再分配程度的数字。 该方法可以用作鉴定调节成分并能够治疗与该成分的功能有关的疾病的化合物的筛选程序。
    • 5. 发明授权
    • Method for extracting quantitative information relating to interactions between cellular components
    • 提取与细胞成分之间相互作用有关的定量信息的方法
    • US07282347B2
    • 2007-10-16
    • US10332065
    • 2001-07-03
    • Sara Petersen BjornOle ThastrupBernard Robert TerryGrith HagelSoren Jensby Nielsen
    • Sara Petersen BjornOle ThastrupBernard Robert TerryGrith HagelSoren Jensby Nielsen
    • C07H21/04C12Q1/68C12N9/12C12N5/06
    • G01N33/6845G01N33/5008G01N33/502G01N33/5032G01N33/68
    • A method is described to assay for protein interactions in living cells, e.g. by the introduction of two heterologous conjugates into the cell. The method uses the measurement of cellular distribution of a detectable component (e.g. a GFP-labeled˜fluorescent probe) to indicate the presence or absence of an interaction between that component and a second component of interest. The method uses the knowledge that certain components can be stimulated to redistribute within the cell to defined locations. Inducible redistribution systems make it possible to determine if specific interactions occur between components. Inducible systems are described where it is demonstrated that the redistribution stimuli are essentially “null”, in that they affect no other system in the cell during the assay period, other than the component whose redistribution can be induced. Also described is an extraction buffer which is useful in high throughput screening for drugs which affect the intracellular distribution of intracellular components. The extraction buffer comprises a cellular fixation agent and cellular permeabilisation agent. Optimizing the composition of the extraction buffer and its application to various cell types is described.
    • 描述了一种测定活细胞中蛋白质相互作用的方法,例如 通过将两种异源偶联物引入细胞。 该方法使用可检测组分(例如GFP-标记的〜荧光探针)的细胞分布的测量来指示该组分与感兴趣的第二组分之间存在或不存在相互作用。 该方法使用某些组件可以被激励以在单元格内重新分配到定义的位置的知识。 诱导再分配系统可以确定组件之间是否发生特定的相互作用。 描述了可诱导的系统,其中证明再分布刺激基本上是“无效”的,因为除了可以诱导其再分配的组分之外,它们在测定期间不影响细胞中的其它系统。 还描述了一种提取缓冲液,其可用于影响细胞内组分细胞内分布的药物的高通量筛选。 提取缓冲液包含细胞固定剂和细胞透化剂。 描述了优化提取缓冲液的组成及其在各种细胞类型中的应用。