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公开(公告)号:US07005071B2
公开(公告)日:2006-02-28
申请号:US10699058
申请日:2003-10-31
IPC分类号: B01D15/08
CPC分类号: B01J45/00 , B01D15/3828 , B01J20/286 , B01J20/3251 , B01J20/3265 , C07C323/58 , C07D333/36
摘要: The present invention relates to a method of generating at least one polydentate metal chelating affinity ligand, which method comprises the steps of a) providing at least one cyclic scaffold comprising a carbonyl, an adjacent sulphur and a nucleophile; b) providing at least one polydentate metal chelating affinity ligand arm, optionally in a form wherein the metal chelating functionalities are protected, on each scaffold by derivatisation of the nucleophile of said scaffolds, while retaining the cyclic structure of the scaffold; (c) ring-opening at the bond between the carbonyl and the sulphur of the derivatized scaffold by adding a reagent that adds one or more metal chelating affinity ligand arms to the scaffold; and, if required, (d) deprotecting the functionalities of the ligand arm(s) provided in step (b). In the most preferred embodiment of the method, steps (c) and (d) are performed simultaneously as one single step.
摘要翻译: 本发明涉及产生至少一种多齿金属螯合亲和配体的方法,该方法包括该步骤
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公开(公告)号:US20060027501A1
公开(公告)日:2006-02-09
申请号:US11244603
申请日:2005-10-06
申请人: Lars Andersson , Ulf Tedebark , Tesfai Gebru , Andreas Axen , Jean-Luc Maloisel
发明人: Lars Andersson , Ulf Tedebark , Tesfai Gebru , Andreas Axen , Jean-Luc Maloisel
IPC分类号: B01D15/08
CPC分类号: B01J45/00 , B01D15/3828 , B01J20/286 , B01J20/3251 , B01J20/3265 , C07C323/58 , C07D333/36
摘要: The present invention relates to a method of generating at least one polydentate metal chelating affinity ligand, which method comprises the steps of (a) providing at least one cyclic scaffold comprising a carbonyl, an adjacent sulphur and a nucleophile; (b) providing at least one polydentate metal chelating affinity ligand arm, optionally in a form wherein the metal chelating functionalities are protected, on each scaffold by derivatisation of the nucleophile of said scaffolds, while retaining the cyclic structure of the scaffold; (c) ring-opening at the bond between the carbonyl and the sulphur of the derivatised scaffold by adding a reagent that adds one or more metal chelating affinity ligand arms to the scaffold; and, if required, (d) deprotecting the functionalities of the ligand arm(s) provided in step (b). In the most preferred embodiment of the method, steps (c) and (d) are performed simultaneously as one single step.
摘要翻译: 本发明涉及产生至少一种多齿金属螯合亲和配体的方法,该方法包括以下步骤:(a)提供至少一种包含羰基,相邻硫和亲核试剂的环状支架; (b)在保留支架的环状结构的同时,通过衍生所述支架的亲核试剂,在每个支架上提供至少一种多金属金属螯合亲和配体臂,任选地以金属螯合官能团的形式被保护; (c)通过加入一种将一种或多种金属螯合亲和配体臂添加到支架中的试剂,在衍生化支架的羰基和硫之间的键上开环; 如果需要,(d)使步骤(b)中提供的配体臂的功能脱保护。 在该方法的最优选实施方案中,步骤(c)和(d)同时作为一个步骤进行。
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公开(公告)号:US09944722B2
公开(公告)日:2018-04-17
申请号:US13701074
申请日:2011-05-30
申请人: Mattias Algotsson , Lars C. Andersson , Eggert Brekkan , Lee Hedemyr , Jean-Luc Maloisel , Ronnie Palmgren
发明人: Mattias Algotsson , Lars C. Andersson , Eggert Brekkan , Lee Hedemyr , Jean-Luc Maloisel , Ronnie Palmgren
IPC分类号: C07C237/10 , C08B37/00 , B01J20/289 , B01J20/32 , C07C323/60 , B01J20/281
CPC分类号: C08B37/0039 , B01J20/281 , B01J20/289 , B01J20/3219 , B01J20/3251 , B01J20/3265 , C07C237/10 , C07C323/60
摘要: The present invention relates to dimeric pentadentate chelators with exceptionally strong binding of metal ions, for detection, immobilization and purification of biomolecules. Dimeric chelators offer a cooperativity of binding of two adjacent immobilized metal ions simultaneously to a histidine-tagged biomolecule, which gives advantageous properties regarding strength of binding compared to a corresponding monomer chelator. In addition, a dimer increases the selectivity (ease of separation) against non-tagged biomolecules with low metal-ion affinity.The dimeric pentadentate chelator according to the invention has the following general formula: wherein Sc is a scaffold or a connecting structure that contains at least two functional groups enabling coupling of two pentadentate chelators (PD), and PD is a pentadentate chelator having the formula:
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公开(公告)号:US20130072638A1
公开(公告)日:2013-03-21
申请号:US13701074
申请日:2011-05-30
申请人: Mattias Algotsson , Lars C. Andersson , Eggert Brekkan , Lee Hedemyr , Jean-Luc Maloisel , Ronnie Palmgren
发明人: Mattias Algotsson , Lars C. Andersson , Eggert Brekkan , Lee Hedemyr , Jean-Luc Maloisel , Ronnie Palmgren
IPC分类号: C08B37/00 , B01J20/281
CPC分类号: C08B37/0039 , B01J20/281 , B01J20/289 , B01J20/3219 , B01J20/3251 , B01J20/3265 , C07C237/10 , C07C323/60
摘要: The present invention relates to dimeric pentadentate chelators with exceptionally strong binding of metal ions, for detection, immobilization and purification of biomolecules. Dimeric chelators offer a cooperativity of binding of two adjacent immobilized metal ions simultaneously to a histidine-tagged biomolecule, which gives advantageous properties regarding strength of binding compared to a corresponding monomer chelator. In addition, a dimer increases the selectivity (ease of separation) against non-tagged biomolecules with low metal-ion affinity.The dimeric pentadentate chelator according to the invention has the following general formula: whereinSc is a scaffold or a connecting structure that contains at least two functional groups enabling coupling of two pentadentate chelators (PD), andPD is a pentadentate chelator having the formula:
摘要翻译: 本发明涉及具有非常强的金属离子结合的二聚五齿螯合物,用于生物分子的检测,固定和纯化。 二聚螯合剂提供了两个相邻的固定化金属离子与组氨酸标记的生物分子的结合的协同作用,与对应的单体螯合剂相比,其对结合强度具有有利的性质。 此外,二聚体增加了具有低金属离子亲和力的非标记生物分子的选择性(易于分离)。 根据本发明的二聚五齿螯合剂具有以下通式:其中Sc是含有至少两个能够偶合两种五齿螯合剂(PD)的官能团的支架或连接结构,PD是具有下式的五齿螯合剂:
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公开(公告)号:US08217118B2
公开(公告)日:2012-07-10
申请号:US12094286
申请日:2006-11-22
申请人: Gunnar Glad , Jean-Luc Maloisel , Nicolas Thevenin
发明人: Gunnar Glad , Jean-Luc Maloisel , Nicolas Thevenin
IPC分类号: C07D303/02 , C07H1/00 , C08F8/00
CPC分类号: B01J20/262 , B01J20/261 , B01J20/265 , B01J20/267 , B01J20/28016 , B01J20/286 , B01J20/287 , B01J20/3204 , B01J20/321 , B01J20/3212 , B01J20/3217 , B01J20/3219 , B01J20/3246 , B01J20/3248 , B01J20/3251 , B01J20/3253 , B01J20/3255 , B01J2220/54 , B01J2220/58
摘要: Disclosed is a method for activating a solid support material with epoxy groups and for immobilizing ligands thereon, utilizing phase transfer catalytic conditions. The method permits the introduction of epoxy groups and specific nucleophilic ligands on the support material with a high level of substitution. Furthermore, the invention provides a general method for immobilizing a ligand for use in a wide variety of chromatographic separation procedures such as ion exchange chromatography, hydrophobic interaction chromatography (HIC), reverse phase chromatography (RPC), or affinity chromatography.
摘要翻译: 公开了一种利用相转移催化条件活化具有环氧基团的固体支持材料和固定配体的方法。 该方法允许以高水平的取代在载体材料上引入环氧基团和特定的亲核配体。 此外,本发明提供了用于固定配体以用于各种色谱分离方法如离子交换层析,疏水相互作用层析(HIC),反相色谱(RPC)或亲和层析中的一般方法。
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公开(公告)号:US08092683B2
公开(公告)日:2012-01-10
申请号:US12517570
申请日:2008-01-10
IPC分类号: B01D15/08
CPC分类号: C40B30/04 , B01D15/1885 , B01D15/361 , B01D15/362 , B01D15/363 , B01D15/3847 , B01J20/3285 , B01J39/26 , B01J41/20 , B01J2220/54 , C40B40/14 , C40B50/00 , G01N30/466 , G01N30/96
摘要: The present invention relates to a method of preparing a library of resins which are useful in chromatography, which method comprises creating a diversity of multi-modal ion exchange resins; and providing the diversity in a parallel system in which each resin is presented separated from the other resin(s).
摘要翻译: 本发明涉及一种制备可用于色谱法的树脂文件库的方法,该方法包括产生多种多模式离子交换树脂; 并且在与其它树脂分离出每种树脂的并行系统中提供多样性。
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公开(公告)号:US20110045574A1
公开(公告)日:2011-02-24
申请号:US12988707
申请日:2009-04-21
申请人: Jan Bergstrom , Gunnar Glad , Bo-Lennart Johansson , Jean-Luc Maloisel , Nils Norrman , Tobias E. Soderman
发明人: Jan Bergstrom , Gunnar Glad , Bo-Lennart Johansson , Jean-Luc Maloisel , Nils Norrman , Tobias E. Soderman
IPC分类号: C12N7/02 , H01F1/00 , C12N1/20 , C12N15/63 , B01J20/00 , B01J20/26 , C07K16/00 , C07K1/14 , C07H21/00 , C11B3/00
CPC分类号: B01D15/327 , B01J20/28009 , B01J20/285 , B01J20/287 , B01J20/3212 , B01J20/3293 , B01J39/26 , C07K1/20 , C07K16/00 , C12N7/00 , C12N2760/16151 , G01N1/405
摘要: The present invention is within the field of chromatography. More precisely, it relates to a novel chromatography medium, namely a hydrophobic medium provided with different lids excluding molecules over a certain size due to the porosity of the hydrophobic medium and/or the porosity of the lid. The invention also relates to use of the separation medium for purification of large molecules, which do not enter the separation medium, as well as small molecules, which enter the separation medium and are eluted from there.
摘要翻译: 本发明在色谱领域内。 更准确地说,它涉及一种新颖的色谱介质,即由于疏水介质的孔隙率和/或盖的孔隙度,提供了不同盖子的疏水介质,其中排除了一定尺寸的分子。 本发明还涉及用于纯化不分离介质的大分子的分离介质以及进入分离介质并从其中洗脱的小分子的用途。
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公开(公告)号:US20100121035A1
公开(公告)日:2010-05-13
申请号:US12594002
申请日:2008-03-20
CPC分类号: B01J20/289 , B01D15/32 , B01D15/327 , B01D15/361 , B01D15/3804 , B01D15/3847 , B01J20/262 , B01J20/267 , B01J20/286 , B01J20/3212 , B01J20/3219 , B01J20/3251 , B01J20/3272 , B01J20/328 , B01J20/3285 , B01J2220/54 , B01J2220/58 , C07K1/20 , C07K16/00
摘要: The present invention relates to a separation matrix comprised of a porous or non-porous support to which ligands have been immobilised, wherein said ligands comprise at least one aliphatic sulfamide. The invention also relates to a chromatography column that contains the described separation matrix, as well as to a method of isolating immunoglobulins, such as IgG, Fab fragments, fusion proteins containing immunoglobulins etc, by adsorption to a separation matrix that comprises the aliphatic sulfamide ligands of the invention.
摘要翻译: 本发明涉及由已经固定有配体的多孔或无孔载体组成的分离基质,其中所述配体包含至少一个脂族磺酰胺。 本发明还涉及含有所述分离基质的色谱柱,以及通过吸附到包含脂族磺酰胺配体的分离基质上分离免疫球蛋白如IgG,Fab片段,含有免疫球蛋白的融合蛋白等的方法 的本发明。
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公开(公告)号:US20060175258A1
公开(公告)日:2006-08-10
申请号:US10547570
申请日:2004-03-05
CPC分类号: B01J20/3285 , B01D15/325 , B01D15/327 , B01J20/286
摘要: The invention is a method of preparing multimodal ligands for hydrophobic interaction chromatography (HIC), which comprises providing a cyclic scaffold comprising a thiol, an amine and a carbonyl group; derivatisation of the nitrogen with a reagent to introduce a primary interaction; and aminolysis of the resulting derivative, whereby a secondary interaction is introduced next to the carbonyl; wherein at least one of the primary interaction and the secondary interaction comprises a hydrophobic group and wherein non of said interactions comprises charged groups, i.e. ion exchange ligands. The invention also encompasses a separation medium comprising such multimodal ligands immobilised to a base matrix.
摘要翻译: 本发明是制备用于疏水相互作用色谱(HIC)的多峰配体的方法,其包括提供包含硫醇,胺和羰基的环状支架; 用试剂衍生氮以引入主要相互作用; 和所得衍生物的氨解,由此在羰基旁边引入二次相互作用; 其中所述主要相互作用和所述第二相互作用中的至少一种包含疏水基团,并且其中所述相互作用中的非相互作用包括带电基团,即离子交换配体。 本发明还包括一种分离介质,其包含固定在基础基质上的这种多峰配体。
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10.
公开(公告)号:US20050100878A1
公开(公告)日:2005-05-12
申请号:US10398439
申请日:2001-10-02
IPC分类号: G01N27/62 , G01N27/447 , G01N27/64 , G01N30/06 , G01N30/72 , G01N30/88 , G01N33/68 , C12Q1/00
CPC分类号: G01N33/6803
摘要: The present invention relates to a method for the quantitative determination of the amount of one or more biomolecules, such as proteins or polypeptides, in one or more samples by utilising sample unique tagging reagents. More specifically, the method comprises steps of providing at least two samples; reacting biomolecules present in each sample with a sample unique mass tagging reagent to provide sample unique mass tagged forms thereof; combining tagged forms present in each sample to provide a single sample; coseparating, from the resulting sample, a mix of mass tagged forms of each of said biomolecules into different fractions; subjecting, for each fraction, the mix to mass spectrometry to obtain a mass spectrum; and determining from signals in each mass spectrum, the amount of the biomolecule corresponding to the spectrum in at least one of said samples relative to the amount of the same biomolecule in at least one of the remaining samples. In an advantageous embodiment, the separation step is a gel electrophoresis step. In some cases, it may be advantageous to also include a step of digesting biomolecules, such as protein(s).
摘要翻译: 本发明涉及通过利用样品独特标记试剂在一个或多个样品中定量测定一种或多种生物分子(例如蛋白质或多肽)的量的方法。 更具体地,该方法包括提供至少两个样本的步骤; 使每个样品中存在的生物分子与样品独特的质量标签试剂反应,以提供样品独特的质量标签形式; 组合每个样品中存在的标记形式以提供单个样品; 从所得样品中分离出每种所述生物分子的质量标签形式的混合物到不同的级分; 对每个级分进行混合物进行质谱分析以获得质谱; 并且从每个质谱图中的信号确定与至少一个剩余样品中相同生物分子的量相对应的至少一个所述样品中的光谱的生物分子的量。 在有利的实施方案中,分离步骤是凝胶电泳步骤。 在一些情况下,还可以包括消化生物分子如蛋白质的步骤是有利的。
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