JP6157046B2 - 静電的ステアリング(electrostaticsteering)効果を用いた抗体Fcヘテロ二量体分子を作製するための方法 - Google Patents
静電的ステアリング(electrostaticsteering)効果を用いた抗体Fcヘテロ二量体分子を作製するための方法 Download PDFInfo
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/46—Hybrid immunoglobulins
- C07K16/468—Immunoglobulins having two or more different antigen binding sites, e.g. multifunctional antibodies
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/52—Constant or Fc region; Isotype
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/52—Constant or Fc region; Isotype
- C07K2317/526—CH3 domain
Description
表2b:静電的ステアリング効果を増進するためのさらなる単一電荷残基突然変異a
各正電荷残基(LysおよびArg)を2つの負電荷残基(AspまたはGlu)に突然変異させてもよいし、そして逆も可能であり、そしてその結果、本明細書に記載する方法は、多くの組み合わせを提供する。本明細書において、突然変異部位を取り巻く残基および水分子の役割に応じて、異なる組み合わせが四次(ホモ二量体/ヘテロ二量体)構造形成に多様な影響を及ぼすであろうことを述べなければならない。アミノ酸ヒスチジン(His)は、中性pHでは正電荷であり、そしてしたがってHisに対する突然変異もまた意図される。しかし、負電荷残基(AspまたはGlu)をHisに突然変異させると、側鎖体積が増加し、これが立体問題を引き起こす可能性もある。さらに、ヒスチジン・プロトンドナーおよびアクセプター型は、局所環境に応じる。設計戦略中、これらの問題を考慮に入れなければならない。
接合部分内のカッパ軽鎖−重鎖接触を表5に示す。
本実施例は、静電的ステアリング効果を用いて、ホモ二量体化を不利にしつつ、ヘテロ二量体化を有利にするように、CH3ドメインを操作可能であることを立証する。CH3ドメイン接合部分に電荷残基突然変異を有する、図8(a)に示すようなマキシボディ−ダミーFc構築物を作製した。SDSポリアクリルアミドゲル電気泳動を通じて、ホモ二量体およびヘテロ二量体収量の形成を評価した。マキシボディは、ダミーFcに比較して、より高い分子量を有するため、ヘテロ二量体(マキシボディ−ダミーFc)およびホモ二量体(マキシボディ−マキシボディおよびダミーFc−ダミーFc)は、SDS−PAGE上で異なる移動度を有し、これによって、多様な対形成の同定が容易になる(図8(b))。
K409近くに位置する電荷残基、例えばK360およびK392で、さらなる突然変異を導入した際、ヘテロ二量体形成のさらなる増加が観察された(図10)。例えば、ダミーFc上のK409D;K392DとM315マキシボディ上のD399’Kを組み合わせると、ホモ二量体に対するヘテロ二量体の比の増加が示され、これはおそらくFcホモ二量体の破壊のためである。Fc単量体のサイズに対応する25KDのバンドが、K409D;K392DダミーFcを用いたすべてのトランスフェクション上で検出された(データ未提示)。M315マキシボディのD399’K変異体に加えてD356’KまたはD357’Kなどの別の突然変異を付加すると、さらなる改善が示された。ダミーFc上のK409D;K392DとM315マキシボディ上のD399’K;D356’Kを組み合わせると、ヘテロ二量体がほぼ排他的に形成された。K409D;K392D/D399’K;D357’KおよびK409D;K370D/D399’K;D357’Kなどの他の組み合わせもまた、K409D/D399’K変異体より有意な改善を提供した。
実施例2
本実施例は、特定の三重電荷対突然変異が、単独で発現された場合にホモ二量体を形成不能であるが、同時発現された場合にヘテロ二量体を形成可能であったことを立証する。実施例1に記載するように、突然変異体を作製し、そして細胞をトランスフェクションした。構築物を同時トランスフェクションする際には、1:1のプラスミド比を用いた。結果を図11に示す。ヤギ抗ヒトFc HRPコンジュゲート化抗体を用いたウェスタンブロットによって、ヘテロ二量体およびホモ二量体を検出した。興味深いことに、正電荷残基を負電荷残基に変化させた(K409D、K392D、K370DまたはK409D、K392D、K439D)三重突然変異を有するFc含有分子は、単独で発現させた際、検出不能であった。同様に、負電荷残基を正電荷残基に変化させた(D399K、E356K、E357K)三重突然変異を有するFc含有分子は、単独で発現させた際、検出不能であった。しかし、反対の電荷極性の突然変異を有するFc含有分子と同時発現させると、ヘテロ二量体のみが検出された。
Claims (11)
- 集合して、ヘテロ二量体形成を促進するように操作された接合部分を形成する、第一のCH3ドメインおよび第二のCH3ドメインを含むヘテロ二量体タンパク質であって、
前記の第一のCH3ドメインおよび前記の第二のCH3ドメインのそれぞれはIgGのCH3ドメインであり、
前記の第一のCH3ドメインが、Lys392およびLys409の負電荷アミノ酸での置換を含み、そして前記の第二のCH3ドメインが、Asp399およびGlu356の正電荷アミノ酸での置換を含む、前記ヘテロ二量体タンパク質。 - ヒトIgG Fc領域を含む、請求項1に記載のヘテロ二量体タンパク質。
- ヒトIgG Fc領域がIgG1 Fc領域を含む、請求項2に記載のヘテロ二量体タンパク質。
- 負電荷アミノ酸がアスパラギン酸である、請求項1〜3のいずれか1項に記載のヘテロ二量体タンパク質。
- 正電荷アミノ酸がリジンである、請求項1〜4のいずれか1項に記載のヘテロ二量体タンパク質。
- 第一のCH3ドメインが、Lys370またはLys439の負電荷アミノ酸での置換をさらに含み、及び/又は第二のCH3ドメインが、Glu357の正電荷アミノ酸での置換をさらに含む、請求項1〜5のいずれか1項に記載のヘテロ二量体タンパク質。
- 負電荷アミノ酸がアスパラギン酸である、請求項6に記載のヘテロ二量体タンパク質。
- 正電荷アミノ酸がリジンである、請求項6又は7に記載のヘテロ二量体タンパク質。
- 請求項1〜8のいずれか1項に記載のヘテロ二量体タンパク質を調製する方法であって、当該方法は以下の工程:
(a)第一のCH3ドメインをコードする核酸および第二のCH3ドメインをコードする核酸を含む宿主細胞を培養し、ここで培養された宿主細胞が第一および第二のCH3ドメインを発現し;そして
(b)宿主細胞培養からヘテロ二量体タンパク質を回収する;
を含む、前記方法。 - 請求項1〜8のいずれか1項に記載のヘテロ二量体タンパク質を製造するための宿主細胞であって、第一のCH3ドメインをコードする核酸および第二のCH3ドメインをコードする核酸を含む、前記宿主細胞。
- 請求項1〜8のいずれか1項に記載のヘテロ二量体タンパク質を含む医薬組成物。
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US1956908P | 2008-01-07 | 2008-01-07 | |
US61/019,569 | 2008-01-07 | ||
US12030508P | 2008-12-05 | 2008-12-05 | |
US61/120,305 | 2008-12-05 | ||
PCT/US2009/000071 WO2009089004A1 (en) | 2008-01-07 | 2009-01-06 | Method for making antibody fc-heterodimeric molecules using electrostatic steering effects |
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JP2015215539A Division JP6328087B2 (ja) | 2008-01-07 | 2015-11-02 | 静電的ステアリング(electrostaticsteering)効果を用いた抗体Fcヘテロ二量体分子を作製するための方法 |
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JP2015215539A Active JP6328087B2 (ja) | 2008-01-07 | 2015-11-02 | 静電的ステアリング(electrostaticsteering)効果を用いた抗体Fcヘテロ二量体分子を作製するための方法 |
JP2018078924A Active JP6703560B2 (ja) | 2008-01-07 | 2018-04-17 | 静電的ステアリング(electrostatic steering)効果を用いた抗体Fcヘテロ二量体分子を作製するための方法 |
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JP2018078924A Active JP6703560B2 (ja) | 2008-01-07 | 2018-04-17 | 静電的ステアリング(electrostatic steering)効果を用いた抗体Fcヘテロ二量体分子を作製するための方法 |
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JP (3) | JP6157046B2 (ja) |
AU (1) | AU2009204501B2 (ja) |
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CY (1) | CY1117162T1 (ja) |
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JP6328087B2 (ja) | 2018-05-23 |
EP2235064B1 (en) | 2015-11-25 |
US20100286374A1 (en) | 2010-11-11 |
US8592562B2 (en) | 2013-11-26 |
CY1117162T1 (el) | 2017-04-05 |
US20140024111A1 (en) | 2014-01-23 |
EP3663318A1 (en) | 2020-06-10 |
ES2774337T3 (es) | 2020-07-20 |
JP6703560B2 (ja) | 2020-06-03 |
JP2016093175A (ja) | 2016-05-26 |
PL2235064T3 (pl) | 2016-06-30 |
DK2235064T3 (en) | 2016-01-11 |
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