JP2000506392A - 新規なヒト代謝指向型グルタミン酸レセプター - Google Patents
新規なヒト代謝指向型グルタミン酸レセプターInfo
- Publication number
- JP2000506392A JP2000506392A JP9540300A JP54030097A JP2000506392A JP 2000506392 A JP2000506392 A JP 2000506392A JP 9540300 A JP9540300 A JP 9540300A JP 54030097 A JP54030097 A JP 54030097A JP 2000506392 A JP2000506392 A JP 2000506392A
- Authority
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- Japan
- Prior art keywords
- nucleic acid
- seq
- receptor
- sequence
- metabotropic glutamate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1. 配列番号1のアミノ酸配列を有する代謝指向型グルタミン酸レセプター蛋 白質のユニーク部分の少なくとも5個の連続アミノ酸残基をコードし、前記ユニ ーク部分をコードしない他の核酸分子から分離された、少なくとも15ヌクレオ チドの長さの精製されたまたは単離された核酸分子。 2. 代謝指向型グルタミン酸レセプター蛋白質がヒト蛋白質である、請求項1 記載の核酸分子。 3. ゲノムDNA配列、cDNA配列またはRNA配列を含む、請求項1記載 の核酸分子。 4. 前記代謝指向型グルタミン酸レセプター蛋白質が配列番号1の残基1−8 93のアミノ酸配列を含む、請求項1記載の核酸分子。 5. 前記部分が配列番号1の残基1−893のアミノ酸配列を含む、請求項1 または4に記載の核酸分子。 6. 前記核酸分子が配列番号1の残基1−893のアミノ酸配列を含む代謝指 向型グルタミン酸レセプター蛋白質をコードする、請求項1記載の核酸分子。 7. 前記核酸分子が、配列番号1のアミノ酸配列を含む代謝指向型グルタミン 酸レセプター蛋白質をコードする、請求項1記載の核酸分子。 8. 配列番号5の配列を含む、請求項7記載の核酸分子。 9. 配列番号5の核酸配列またはこれに実質的に相補的な配列の少なくとも1 5個の連続ヌクレオチドを含む、請求項1記載の核酸分子。 10. 配列番号5の核酸配列またはこれに実質的に相補的な配列の少なくとも 50個の連続ヌクレオチドを含む、請求項9記載の精製された核酸分子。 11. 前記核酸がさらに、配列番号5のヌクレオチド2678−2724に与 えられる核酸配列の少なくとも15個の連続ヌクレオチドを含む、請求項9記載 の核酸分子。 12. 配列番号5に与えられる核酸配列の少なくとも15個の連続ヌクレオチ ドを含み、ここで、前記ヌクレオチド配列がさらに配列番号5のヌクレオチド2 678−2724に与えられる配列の少なくとも3個の連続ヌクレオチドを含む 、 請求項9記載の核酸分子。 13. 前記5個の連続アミノ酸残基の少なくとも1つが、配列番号1の残基8 94−908の1つである、請求項1記載の核酸分子。 14. 前記核酸分子が、配列番号1のアミノ酸残基894−908を含むアミ ノ酸配列をコードする、請求項13記載の核酸分子。 15. 配列番号1のアミノ酸配列に含まれる細胞外ドメインを含むアミノ酸配 列をコードし、ここでコードされるアミノ酸配列は膜貫通ドメインおよび細胞内 ドメイン部分を実質的に含まない請求項1記載の核酸分子、またはこれに実質的 に相補的な配列を有する核酸分子。 16. 前記核酸分子が非代謝指向型グルタミン酸レセプターの膜貫通ドメイン および細胞内ドメインをコードする第2の核酸分子と転写的に結合している請求 項15記載の核酸分子、またはこれに実質的に相補的な配列を有する核酸分子。 17. 配列番号1のアミノ酸配列に含まれる細胞外ドメインおよび膜貫通ドメ インを含むアミノ酸配列をコードしており、ここで、コードされるアミノ酸配列 は細胞内ドメイン部分を実質的に含まない請求項1記載の核酸分子、またはこれ に実質的に相補的な配列を有する核酸分子。 18. 請求項1、6または7のいずれかに記載の核酸分子に実質的に相補的な 核酸配列を有する、単離されたまたは精製された核酸分子。 19. 配列番号1に与えられるアミノ酸配列の少なくとも6個の連続アミノ酸 を含む、精製されたポリペプチド。 20. 前記アミノ酸配列の少なくとも18個の連続アミノ酸を含む、請求項1 9記載の精製されたポリペプチド。 21. さらに、配列番号1の残基894−908に与えられる配列の少なくと も1個の連続アミノ酸を含む、請求項19記載の精製されたポリペプチド。 22. 配列番号1の残基894−908に与えられるアミノ酸配列を含む、請 求項21記載の精製されたポリペプチド。 23. 請求項1、6または7のいずれかに記載の核酸分子を含む、生物学的に 機能性の発現ベクター。 24. 請求項23記載の発現ベクターによりトランスフォームまたはトランス フェクトされた、原核生物または真核生物宿主細胞。 25. 前記宿主細胞が脊椎動物細胞である、請求項24記載の宿主細胞。 26. ポリペプチド生成物を製造する方法であって、請求項7記載の発現ベク ターでトランスフォームまたはトランスフェクトされた原核生物または真核生物 宿主細胞を、適した栄養条件下で、前記発現ベクターに挿入された前記核酸分子 によりコードされるポリペプチド生成物の発現を可能とする様式で増殖させるこ とを含む方法。 27. さらに、前記ポリペプチド生成物の単離を含む、請求項26記載の方法 。 28. トランスジェニック哺乳動物を作成する方法であって、配列番号1のア ミノ酸配列を有する蛋白質またはその生物学的に活性な部分をコードする核酸配 列から本質的になる核酸分子を非ヒト哺乳動物に挿入する工程を含む方法。 29. 配列番号1またはその生物学的に活性な部分から本質的になる代謝指向 型グルタミン酸レセプターに結合するかまたはその活性を調節する化合物をスク リーニングする方法であって、 前記代謝指向型グルタミン酸レセプターおよび可能性のある化合物を許容しうる 媒質に導入し、そして 物理学的に検出可能な手段により結合または調節を監視し、このことにより、前 記代謝指向型グルタミン酸レセプターと相互作用するかまたはその活性を調節す る化合物を同定する、 ことを含む方法。 30. 前記代謝指向型グルタミン酸レセプターが、 配列番号1に含まれるアミノ酸配列を有する細胞外ドメイン、および 配列番号1のアミノ酸配列を有するレセプターとは異なるレセプターの細胞内ド メイン を有するキメラレセプターである、請求項29記載の方法。 31. 標識した既知の結合剤による競合結合アッセイを含む、請求項29記載 の方法。 32. 代謝指向型グルタミン酸レセプターが細胞により発現され、前記化合物 の前記細胞に及ぼす影響を監視することをさらに含む、請求項29記載の方法。 33. 細胞が真核生物細胞である、請求項32記載の方法。 34. 真核生物細胞において発現される、配列番号1の配列を有する代謝指向 型グルタミン酸レセプターの活性を調節する方法であって、 前記レセプターを、前記レセプターのアゴニスト、アンタゴニスト、またはアロ ステリック調節剤として作用する化合物と接触させる工程を含む方法。 35. 代謝指向型グルタミン酸レセプターの活性を調節する方法であって、配 列番号1の配列から本質的になる代謝指向型グルタミン酸レセプターを含む細胞 に、前記代謝指向型グルタミン酸レセプターにおけるグルタミン酸の1つまたは それ以上の効果を模倣するか、または前記代謝指向型グルタミン酸レセプターに おけるグルタミン酸の1つまたはそれ以上の効果を遮断するのに十分な量の代謝 指向型グルタミン酸レセプター調節分子を与える工程を含み、 ここで前記分子は代謝指向型グルタミン酸レセプター活性を調節し、および前記 方法はインビトロまたはインビボで実施されることを特徴とする方法。 36. 前記化合物が、ホスホイノシチド加水分解の増加、ホスホリパーゼCの 活性化、サイトゾルカルシウム(Ca2+)濃度の増加、アデニリルシクラーゼの 活性化、アデニリルシクラーゼの阻害、cAMP形成の増加、cAMP形成の減 少、およびアラキドン酸形成の増加、グアニリルシクラーゼの活性化、環状GM P形成の増加、内向き整流カリウムチャネルの活性化、電圧依存性カルシウムチ ャネルの阻害からなる群より選択される1つまたはそれ以上の活性を生成する、 請求項35記載の方法。 37. 患者を治療する方法であって、療法上有効な量の、配列番号1の配列か ら本質的になる機能性代謝指向型グルタミン酸レセプターをコードする核酸を前 記患者に投与する工程を含む方法。 38. 患者を治療する方法であって、療法上有効な量の、配列番号1の配列か ら本質的になる代謝指向型グルタミン酸レセプターの発現を特異的に阻害する核 酸を前記患者に投与することを含む方法。 39. 患者を治療する方法であって、療法上有効な量の、配列番号1の配列を 有する代謝指向型グルタミン酸レセプターの活性を調節する化合物を前記患者に 投与することを含む方法。 40. 前記患者が、グルタミン酸興奮毒性、全体性および病巣性虚血性および 出血性発作、頭部外傷、脊髄損傷、低酸素症誘導性神経細胞損傷、てんかん、ま たはアルツハイマー病、パーキンソン病、またはハンチントン病などの神経変性 性疾病からなる群より選択される神経学的疾病または疾患を有する、請求項39 記載の方法。 41. 前記化合物が、痙攣、神経防御、ニューロン死、ニューロン発達、心臓 活動の中枢制御、覚醒、運動制御および前庭眼反射の制御からなる群より選択さ れる生理学的活性に影響を有する、請求項39記載の方法。 42. a) 配列番号1の配列から本質的になる代謝指向型グルタミン酸レセ プターまたはその機能的均等物に結合するかまたはその活性を調節する化合物、 および b) 生理学的に許容しうる担体 を含む医薬組成物。 43. 配列番号1または配列番号1の残基1−893に与えられるアミノ酸配 列を含むポリペプチドに結合しうる分子、および薬学的に許容しうる緩衝液を含 む、代謝指向型グルタミン酸レセプター結合剤。 44. 前記結合剤が精製された抗体である、請求項43記載の結合剤。 45. 前記抗体が毒素と結合されている、請求項44記載の結合剤。 46. 前記結合剤が前記ポリペプチドに優先的に結合する、請求項43記載の 結合剤。 47. 患者における疾病の診断の方法であって、 a) 前記患者における、配列番号1の配列から本質的になる1つまたはそれ以 上の代謝指向型グルタミン酸レセプターの数または位置を同定し;そして b) 前記数または位置を、正常患者または前記疾病もしくは状態を有すること が知られている患者において見いだされる数または位置と比較する、 の各工程を含む方法。
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US08/604,298 US6084084A (en) | 1996-02-21 | 1996-02-21 | Human metabotropic glutamate receptor |
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PCT/US1997/009025 WO1997048724A2 (en) | 1996-02-21 | 1997-02-20 | Human metabotropic glutamate receptor |
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- 1996-02-21 US US08/604,298 patent/US6084084A/en not_active Expired - Fee Related
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1997
- 1997-02-20 WO PCT/US1997/009025 patent/WO1997048724A2/en active IP Right Grant
- 1997-02-20 JP JP9540300A patent/JP2000506392A/ja active Pending
- 1997-02-20 AT AT97933988T patent/ATE369385T1/de not_active IP Right Cessation
- 1997-02-20 CA CA002246751A patent/CA2246751A1/en not_active Abandoned
- 1997-02-20 AU AU37156/97A patent/AU719841B2/en not_active Ceased
- 1997-02-20 DE DE69737990T patent/DE69737990T2/de not_active Expired - Fee Related
- 1997-02-20 EP EP97933988A patent/EP0882065B1/en not_active Expired - Lifetime
- 1997-02-20 ES ES97933988T patent/ES2292193T3/es not_active Expired - Lifetime
- 1997-02-20 IL IL12571197A patent/IL125711A0/xx active IP Right Grant
- 1997-03-24 US US08/823,110 patent/US6077675A/en not_active Expired - Fee Related
- 1997-03-24 US US08/823,437 patent/US6051688A/en not_active Expired - Fee Related
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1998
- 1998-08-09 IL IL125711A patent/IL125711A/en not_active IP Right Cessation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008516606A (ja) * | 2004-10-14 | 2008-05-22 | カーネギー インスチチューション オブ ワシントン | 神経伝達物質センサーおよびそれを用いる方法 |
JP2013059335A (ja) * | 2004-10-14 | 2013-04-04 | Carnegie Institution Of Washington | 神経伝達物質センサーおよびそれを用いる方法 |
Also Published As
Publication number | Publication date |
---|---|
WO1997048724A2 (en) | 1997-12-24 |
ATE369385T1 (de) | 2007-08-15 |
AU719841B2 (en) | 2000-05-18 |
ES2292193T3 (es) | 2008-03-01 |
AU3715697A (en) | 1998-01-07 |
EP0882065A2 (en) | 1998-12-09 |
CA2246751A1 (en) | 1997-12-24 |
US6051688A (en) | 2000-04-18 |
WO1997048724A3 (en) | 1998-03-26 |
IL125711A0 (en) | 1999-04-11 |
EP0882065B1 (en) | 2007-08-08 |
DE69737990D1 (de) | 2007-09-20 |
US6084084A (en) | 2000-07-04 |
US6077675A (en) | 2000-06-20 |
DE69737990T2 (de) | 2008-09-11 |
IL125711A (en) | 2006-09-05 |
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