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    • 3. 发明授权
    • Fluorescent haloalkyl derivatives of reporter molecules well retained in
cells
    • 报道分子的荧光卤代烷基衍生物保留在细胞中
    • US5362628A
    • 1994-11-08
    • US26633
    • 1993-03-05
    • Richard P. HauglandYu-Zhong ZhangRam SabnisNels A. OlsonJohn J. NalewayRosaria P. Haugland
    • Richard P. HauglandYu-Zhong ZhangRam SabnisNels A. OlsonJohn J. NalewayRosaria P. Haugland
    • C12Q1/04C12Q1/34G01N33/535C12Q1/00A61K37/02C07H15/24G01N33/40
    • C12Q1/04C12Q1/34G01N33/535C12Q2334/00C12Q2334/20C12Q2334/40C12Q2337/20G01N2333/924Y10S530/802
    • The subject invention provides a method for analyzing the metabolic activity in cells by improving the retention of a detectable reporter molecule only in intact cells where a particular enzyme is present. In particular, improved retention results from a two part process involving conjugation of haloalkyl-substituted derivatives of a reporter molecule with intracellular cysteine-containing peptides while unblocking the reporter molecule. The method for analyzing metabolic activity of cells involves the use of a substrate having the formXR-REPORTER-BLOCKwherein -BLOCK is a group selected to be removable by action of a specific analyte, to give REPORTER spectral properties different from those of the substrate,-REPORTER- is a molecule that, when no longer bound to BLOCK by a BLOCK-REPORTER bond, has spectral properities different from those of the substrate, andXR-- is a haloalkyl moiety that can covalently react with an intracellular thiol (Z--S--H) to form a thioether conjugate (Z--S--R--).After the substrate enters the cells, the analyte removes BLOCK to make REPORTER detectable by the change in spectral properties, and the haloalkyl XR reacts with the intracellular thiol to form the thioether conjugate inside the cells, which is well-retained in the cells.
    • 本发明提供了通过仅在存在特定酶的完整细胞中改善可检测报道分子的保留来分析细胞中的代谢活性的方法。 特别地,涉及将报道分子的卤代烷基取代的衍生物与含细胞内半胱氨酸的肽结合的两部分方法的改进的保留结果,同时解除报道分子的阻断。 用于分析细胞代谢活性的方法涉及使用具有XR-REPORTER-BLOCK形式的底物,其中-BLOCK是通过特定分析物的作用被选择为可去除的基团,以产生与底物的不同的REPORTER光谱性质 -REPORTER-是一个分子,当不再通过BLOCK-REPORTER键与BLOCK结合时,具有与底物不同的光谱性质,XR-是可以与胞内硫醇(ZSH)共价反应的卤代烷基部分, 以形成硫醚缀合物(ZSR-)。 在底物进入细胞后,分析物除去BLOCK以通过光谱性质的变化使REPORTER可检测到,并且卤代烷基XR与细胞内硫醇反应以在细胞内形成硫醚缀合物,其在细胞中良好保留。
    • 6. 发明授权
    • Lipophilic fluorescent glycosidase substrates
    • 亲脂性荧光糖苷酶底物
    • US5208148A
    • 1993-05-04
    • US623600
    • 1990-12-07
    • Richard P. HauglandJohn J. NalewayYu-zhong Zhang
    • Richard P. HauglandJohn J. NalewayYu-zhong Zhang
    • C07H17/04C12Q1/34
    • C07H17/04C12Q1/34C12Q2334/40
    • The claimed invention relates to a substrate for evaluating glycosidic enzymes comprising a fluorescein derivative of the general formula: ##STR1## wherein GlyX is a carbohydrate bonded to fluorescein by a glycosidic linkage;Y, which may be the same as GlyX or different, is an alkyl ether, an ester, or a glycosidically linked carbohydrate;R is a lipophilic residue containing from 1 to 21 carbon atoms; andL links the R residue to fluorescein.A preferred embodiment of the invention is a non-fluorescent substrate specifically hydrolyzable by a glycosidase inside a cell to yield, after greater than about 2 minutes, a fluorescent detection product excitable at between about 460 nm and 550 nm and with fluorescence observable at an emission wavelength longer than the excitation wavelength, which fluorescent detection product is retained inside a viable cell more than about 2 hours at greater than about 15.degree. C. and which is non-toxic to the cell. A further embodiment of the invention is a method for evaluating a glycosidic enzyme in living plant or animal cells whether the enzyme is present endogenously; present as a result of manipulation of the cell's genome, or added to the cell exogenously, such as by covalently binding the enzyme to a protein to form an enzyme-protein complex that enters the cell.
    • 所要求保护的发明涉及用于评估糖苷酶的底物,其包含以下通式的荧光素衍生物:其中GlyX是通过糖苷键与荧光素键合的碳水化合物; 可以与GlyX相同或不同的Y是烷基醚,酯或糖苷连接的碳水化合物; R是含有1至21个碳原子的亲脂性残基; 并且L将R残基连接到荧光素上。 本发明的优选实施方案是由细胞内的糖苷酶特异性水解的非荧光底物,大于约2分钟后,可在约460nm至550nm之间激发荧光检测产物,并在发射时可观察到荧光 波长比激发波长长,该荧光检测产物在大于约15℃下在活细胞内保留超过约2小时,对细胞无毒性。 本发明的另一个实施方案是用于评价活体植物或动物细胞中糖苷酶是否内源性存在的方法; 作为细胞基因组的操作或外源性加入到细胞中的结果,例如通过将酶与蛋白质共价结合以形成进入细胞的酶 - 蛋白质复合物。
    • 8. 发明授权
    • Long wavelength lipophilic fluorogenic glycosidase substrates
    • 长波长磷酸荧光蛋白酶底物
    • US5242805A
    • 1993-09-07
    • US749255
    • 1991-08-23
    • John J. NalewayYu-zhong ZhangRichard P. Haugland
    • John J. NalewayYu-zhong ZhangRichard P. Haugland
    • C07H17/00C12Q1/34
    • C12Q1/34C07H17/00C12Q2334/00G01N2333/924
    • The claimed invention relates to a substrate for evaluating glycosidic enzymes comprising a resorufin derivative of the general formula: ##STR1## wherein Gly is a carbohydrate bonded to resorufin by a glycosidic linkage; where at least one of substituents R.sub.1, R.sub.2, R.sub.4, R.sub.6, R.sub.8, and R.sub.9 is a lipophilic residue of the formula --L(CH.sub.2).sub.n CH.sub.3, where n is greater than 3 and less than 22, and where L is a methylene --CH.sub.2 --, an amide --NHCO--, a sulfonamide --NHSO.sub.2 --, a carboxamide --CONH--, a carboxylate ester --COO--, a urethane --NHCOO--, a urea --NHCONH--, or a thiourea --NHCSNH--; andwhere the remainder of substituents R.sub.1, R.sub.2, R.sub.4, R.sub.6, R.sub.8, and R.sub.9, which may be the same or different, are hydrogen, halogen, or other lipophilic residues, which may be the same or different, containing from about 1 to about 22 carbon atoms of the formula --L'(CH.sub.2).sub.m CH.sub.3, where m is less than 22, and where L' is a methylene --CH.sub.2 --, an amide --NHCO--, a sulfonamide --NHSO.sub.2 --, a carboxamide --CONH--, a carboxylate ester --COO--, a urethane --NHCOO--, a urea --NHCONH--, or a thiourea --NHCSNH--.A preferred embodiment of the invention is a non-fluorescent substrate specifically hydrolyzable by a glycosidase inside a cell to yield, after greater than about 2 minutes, an orange to red fluorescent detection product which is retained inside a viable cell more than about 2 hours at greater than about 15.degree. C. and which is non-toxic to the cell. The substrates are used for evaluating a glycosidic enzyme in living plant or animal cells whether the enzyme is present endogenously; present as a result of manipulation of the cell's genome, or added to the cell exogenously, such as by covalently binding the enzyme to a protein to form an enzyme-protein complex that enters the cell.
    • 所要求保护的发明涉及用于评估糖苷酶的底物,其包含通式如下的再生烯衍生物:其中Gly是通过糖苷键键合至残留的碳水化合物; 其中取代基R 1,R 2,R 4,R 6,R 8和R 9中的至少一个是式-L(CH 2)n CH 3的亲脂性残基,其中n大于3且小于22,并且其中L是亚甲基 - CH 2 - ,酰胺-NHCO-,磺酰胺-NHSO 2 - ,酰胺-CONH-,羧酸酯-COO-,氨基甲酸酯-NHCOO-,脲-NHCONH-或硫脲-NHCSNH-; 并且其中可以相同或不同的取代基R 1,R 2,R 4,R 6,R 8和R 9的其余部分是氢,卤素或可以相同或不同的其它亲脂性残基,其含有约1至 约22个碳原子的式-L'(CH 2)m CH 3,其中m小于22,其中L'是亚甲基-CH 2 - ,酰胺-NHCO-,磺酰胺-NHSO 2 - ,甲酰胺-CONH- ,羧酸酯-COO-,氨基甲酸酯-NHCOO-,脲-NHCONH-或硫脲-NHCSNH-。 本发明的优选实施方案是特异性可由细胞内的糖苷酶水解的非荧光底物,大于约2分钟后,产生橙色至红色荧光检测产物,其在活细胞内保留超过约2小时 大于约15℃,对细胞无毒性。 底物用于评价活体植物或动物细胞中的糖苷酶,无论酶是否内源性存在; 作为细胞基因组的操作或外源性加入到细胞中的结果,例如通过将酶与蛋白质共价结合以形成进入细胞的酶 - 蛋白质复合物。
    • 10. 发明授权
    • Antibody complexes and methods for immunolabeling
    • 抗体复合物和免疫标记方法
    • US08323903B2
    • 2012-12-04
    • US10118204
    • 2002-04-05
    • Robert A. ArcherJoseph M. BeechemDavid C. HagenRichard P. HauglandRosaria P. Haugland
    • Robert A. ArcherJoseph M. BeechemDavid C. HagenRichard P. HauglandRosaria P. Haugland
    • G01N33/53
    • B82Y30/00B82Y5/00B82Y10/00G01N33/53G01N33/58G01N33/6857
    • The present invention provides novel immunolabeling complexes and certain components of such complexes, as well as methods of preparing and using such complexes, and kits for use in preparing labeling proteins and for immunolabeling. The pre-formed immunolabeling complexes of the invention comprise both a target-binding antibody and a labeling protein that contains covalently attached labels, where the labeling protein binds selectively and with high affinity to a selected region of the target-binding antibody. Novel labeling proteins of the invention include non-antibody peptides and proteins, such as a complex of protein G and a labeled albumin, and monovalent antibody fragments, such as labeled Fab fragments of an anti-Fc antibody. In methods of the invention, the preformed immunolabeling complexes are added to the sample alone or in combination, for purposes of labeling and optionally detecting the target of interest.
    • 本发明提供了新的免疫标记复合物和这些复合物的某些成分,以及制备和使用这些复合物的方法,以及用于制备标记蛋白和免疫标记的试剂盒。 本发明的预先形成的免疫粘附复合物包含靶结合抗体和含有共价连接的标记的标记蛋白,其中所述标记蛋白选择性地结合并且与靶结合抗体的选定区域具有高亲和力。 本发明的新型标记蛋白包括非抗体肽和蛋白质,例如蛋白G和标记的白蛋白的复合物,以及单价抗体片段,例如抗Fc抗体的标记的Fab片段。 在本发明的方法中,为了标记和任选地检测目的靶标,将预先形成的免疫标记复合物单独或组合加入到样品中。