JP2016511405A5 - - Google Patents

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Publication number
JP2016511405A5
JP2016511405A5 JP2015560136A JP2015560136A JP2016511405A5 JP 2016511405 A5 JP2016511405 A5 JP 2016511405A5 JP 2015560136 A JP2015560136 A JP 2015560136A JP 2015560136 A JP2015560136 A JP 2015560136A JP 2016511405 A5 JP2016511405 A5 JP 2016511405A5
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JP
Japan
Prior art keywords
receptor protein
ligand
cell
organelle
binding molecule
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Pending
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JP2015560136A
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English (en)
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JP2016511405A (ja
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Priority claimed from PCT/PT2014/000016 external-priority patent/WO2014133405A2/en
Publication of JP2016511405A publication Critical patent/JP2016511405A/ja
Publication of JP2016511405A5 publication Critical patent/JP2016511405A5/ja
Pending legal-status Critical Current

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Claims (1)

  1. 細胞内で細胞表面に発現した受容体タンパク質とその同族リガンドの間の相互作用をブロック又は妨害する結合性分子を選択する方法であって、
    前記細胞において、前記細胞の表面で発現可能な受容体タンパク質を発現させるステップ、
    前記細胞において、前記受容体タンパク質の同族リガンドを発現させるステップであって、細胞内オルガネラにおける前記リガンドの保持、及び前記オルガネラにおける前記受容体タンパク質と前記同族リガンドの相互作用を可能にする条件下で、前記同族リガンドが、前記リガンドを細胞内オルガネラにおいて保持するための配列で分子的にタグ付けされているステップ、
    前記細胞内オルガネラにおいて保持されている前記受容体タンパク質又は前記リガンドタンパク質のいずれかを特異的に結合する結合性分子又はその結合性断片若しくは部分を前記細胞に導入するステップ、及び
    前記細胞表面で発現した前記受容体タンパク質のレベルを検出するステップを含み、
    前記結合性分子又はその結合性断片若しくは部分が、前記オルガネラにおいて前記受容体と前記同族リガンドの結合をブロック又は妨害する場合、前記受容体タンパク質が、前記細胞表面で発現及び検出可能であり、前記受容体タンパク質とリガンドの相互作用をブロック又は妨害する前記結合性分子又はその結合性断片若しくは部分が選択可能である、前記方法。

JP2015560136A 2013-03-01 2014-03-03 結合性タンパク質相互作用及び結合性分子の選択及び多様化のための細胞に基づく方法 Pending JP2016511405A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361771562P 2013-03-01 2013-03-01
US61/771,562 2013-03-01
PCT/PT2014/000016 WO2014133405A2 (en) 2013-03-01 2014-03-03 Cell-based methods for coupling protein interactions and binding molecule selection and diversification

Publications (2)

Publication Number Publication Date
JP2016511405A JP2016511405A (ja) 2016-04-14
JP2016511405A5 true JP2016511405A5 (ja) 2017-04-06

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JP2015560136A Pending JP2016511405A (ja) 2013-03-01 2014-03-03 結合性タンパク質相互作用及び結合性分子の選択及び多様化のための細胞に基づく方法

Country Status (6)

Country Link
US (1) US9487773B2 (ja)
EP (2) EP2962103A2 (ja)
JP (1) JP2016511405A (ja)
ES (1) ES2872048T3 (ja)
PT (1) PT3588089T (ja)
WO (1) WO2014133405A2 (ja)

Families Citing this family (10)

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Publication number Priority date Publication date Assignee Title
KR20230155600A (ko) 2014-04-03 2023-11-10 아이쥐엠 바이오사이언스 인코포레이티드 변형된 j-사슬
KR102435324B1 (ko) 2015-01-20 2022-08-23 아이쥐엠 바이오사이언스 인코포레이티드 종양 괴사 인자(tnf) 수퍼패밀리 수용체 결합 분자 및 그의 용도
ES2874558T3 (es) 2015-03-04 2021-11-05 Igm Biosciences Inc Moléculas de unión a CD20 y usos de las mismas
AU2016329197B2 (en) 2015-09-30 2021-01-21 Igm Biosciences, Inc. Binding molecules with modified J-chain
WO2017059387A1 (en) 2015-09-30 2017-04-06 Igm Biosciences, Inc. Binding molecules with modified j-chain
GB201704115D0 (en) * 2017-03-15 2017-04-26 Oxford Genetics Ltd Method of selecting for antibodies
CN113388638A (zh) * 2021-04-13 2021-09-14 中国人民解放军西部战区总医院 一种同时结合TGFβ和VEGF的双靶点融合蛋白质粒的构建方法
WO2023250481A2 (en) * 2022-06-23 2023-12-28 Fuller Laboratories Rickettsia igm assay
WO2024081807A2 (en) * 2022-10-12 2024-04-18 Massachusetts Institute Of Technology Library-scale methods for polypeptide functional analysis
CN116236584B (zh) * 2023-02-20 2024-03-22 四川大学 一种用于高效递送siRNA的多糖-多肽偶联物

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3832847B2 (ja) * 1992-07-17 2006-10-11 ダナ−ファーバー キャンサー インスティテュート 標的分子の細胞内結合方法
US5605793A (en) * 1994-02-17 1997-02-25 Affymax Technologies N.V. Methods for in vitro recombination
US7179462B2 (en) * 2000-06-02 2007-02-20 University Of Connecticut Health Center α (2) macroglobulin receptor as a heat shock protein receptor and uses thereof
US20070248607A1 (en) * 2005-11-03 2007-10-25 Thomas Spies Negative immunomodulation of immune responses by nkg2d-positive cd4+ cells
US9518254B2 (en) * 2009-05-04 2016-12-13 San Diego State University Research Foundation Compositions and methods for identifying enzyme and transport protein inhibitors
AU2010249470B2 (en) * 2009-05-20 2015-06-25 Novimmune S.A. Synthetic Polypeptide Libraries And Methods For Generating Naturally Diversified Polypeptide Variants

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