JPH07503617A - Tat由来の輸送ポリペプチド - Google Patents
Tat由来の輸送ポリペプチドInfo
- Publication number
- JPH07503617A JPH07503617A JP6506542A JP50654294A JPH07503617A JP H07503617 A JPH07503617 A JP H07503617A JP 6506542 A JP6506542 A JP 6506542A JP 50654294 A JP50654294 A JP 50654294A JP H07503617 A JPH07503617 A JP H07503617A
- Authority
- JP
- Japan
- Prior art keywords
- protein
- seq
- fusion protein
- amino acids
- tat
- 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.)
- Granted
Links
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Abstract
Description
Claims (34)
- 1.カルボキシ末端カーゴ部分とアミノ末端輸送部分とからなる融合タンパク質 であって、 (a)輸送分が: (i)HIV tatタンパク質のアミノ酸49−57の存在;(ii)HIV tatタンパク質のアミノ酸22−36の不在;および、(iii)HIV tatタンパク質のアミノ酸73−86の不在;で特徴付けられ、そして、 (b)カーゴ部分が輸送部分依存性の細胞内送達後に有意な生物学的活性を維持 する、融合タンパク質。
- 2.請求項1に記載の融合タンパク質であって、前記カーゴ部分が、治療用分子 、予防用分子、および診断用分子からなる群より選択される、融合タンパク質。
- 3.カルボキシ末端カーゴ部分とアミノ末端輸送部分とからなる融合タンパク質 であって、該カーゴ部分が、標的細胞に送達後に生物学的活性を維持するヒトパ ピローマウイルスE2リプレッサーからなり、そして該輸送部分が:(a)HI V tatタンパク質のアミノ酸47−58(配列番号:47);(b)HIV tatタンパク質のアミノ酸47−72(配列番号:48);(c)HIV tatタンパク質のアミノ酸38−72(配列番号:49);および、 (d)HIV tatタンパク質のアミノ酸38−58(配列番号:50);か らなる群より選択される、融合タンパク質。
- 4.請求項3に記載の融合タンパク質であって、前記輸送部分の前にアミノ末端 メチオニンがある、融合タンパク質。
- 5.請求項1から4のいずれかに記載の融合タンパク質であって、前記カーゴ部 分がヒトパピローマウイルスE2タンパク質のアミノ酸245−365(配列番 号:51)からなる、融合タンパク質。
- 6.融合タンパク質JB106(配列番号:38)。
- 7.融合タンパク質JB117(配列番号:59)。
- 8.融合タンパク質JB118(配列番号:60)。
- 9.融合タンパク質JB122(配列番号:63)。
- 10.カルボキシ末端カーゴ部分とアミノ末端輸送部分とからなる融合タンパク 質であって、該カーゴ部分が、標的細胞に送達後に生物学的活性を維持するウシ パピローマウイルスE2リプレッサーからなり、そして該輸送部分が:(a)H IV tatタンパク質のアミノ酸47−62(配列番号:52);および、 (b)HIV tatタンパク質のアミノ酸38−62(配列番号:53);か らなる群より選択される、融合タンパク質。
- 11.請求項10に記載の融合タンパク質であらて、前記輸送タンパク質の前に アミノ末端メチオニンがある、融合タンパク質。
- 12.請求項1、2、10、または11のいずれかに記載の融合タンパク質であ って、前記カーゴ部分が、ウシパピローマウイルスE2タンパク質のアミノ酸2 50−410(配列番号:56)からなるE2リプレッサーである、融合タンパ ク質。
- 13.融合タンパク質JB119(配列番号:61)。
- 14.融合タンパク質JB120(配列番号:62)。
- 15.輸送ポリペプチド部分とカーゴ部分とからなる共有結合した化学的複合体 であって: (a)複合体の輸送ポリペプチド部分が:(i)HIV tatタンパク質のア ミノ酸49−57の存在;(ii)HIV tatタンパク質のアミノ酸22− 36の不在;および、(iii)HIV tatタンパク質のアミノ酸73−8 6の不在;で特徴付けられ、そして、 (b)複合体のカーゴ部分が、輸送部分依存性の細胞内送達後に有意な生物学的 活性を維持する、融合タンパク質。
- 16.請求項15に記載の共有結合した化学的複合体であって、前記輸送ポリペ プチド部分が、HIV tatタンパク質のアミノ酸37−72(配列番号:2 )からなる、化学的複合体。
- 17.請求項16に記載の共有結合した化学的複合体であって、前記カーゴ部分 が: (a)ヒトパピローマウイルスE2タンパク質のアミノ酸245−365(配列 番号:51);および、 (b)ヒトパピローマウイルスE2タンパク質のアミノ酸245−365(ここ でアミノ酸300および309はシステインに置換している)(配列番号:55 )、 からなる群より選択される、化学的複合体。
- 18.輸送部分とカーゴ部分とからなる共有結合した化学的複合体であって、前 記輸送ポリペプチドが、HIV tatタンパク質のアミノ酸37−72(配列 番号:2)からなり、そして該カーゴ部分が: (a)ヒトパピローマウイルスE2タンパク質のアミノ酸245−365(配列 番号:51);および、 (b)ヒトパピローマウイルスE2タンパク質のアミノ酸245−365(ここ でアミノ酸300および309がシステインに置換している)(配列番号:55 )、からなる群より選択される、化学的複合体。
- 19.カルボキシ末端カーゴ部分とアミノ末端輸送部分とからなる融合タンパク 質であって、該カーゴ部分がHSV VP16タンパク質のアミノ酸43−41 2からなり、そして該輸送部分がHIV tatタンパク質のアミノ酸47−5 8からなる、融合タンパク質。
- 20.請求項19に記載の融合タンパク質であって、前記輸送部分の前にアミノ 末端メチオニンがある、融合タンパク質。
- 21.輸送ポリペプチド部分とカーゴ部分とからなる共有結合した化学的複合体 であって、該輸送ポリペプチド部分が、HIV tatタンパク質のアミノ酸3 7−72(配列番号:2)からなり、そして該カーゴ部分が: (a)オリゴヌクレオチドNF2(配列番号:44)にアニールするオリゴヌク レオチドNFI(配列番号:43)、および、(b)オリゴヌクレオチドNF4 (配列番号:46)にアニールするオリゴヌクレオチドNF3(配列番号:45 )、からなる群より選択される、化学的複合体。
- 22.請求項1から14、19、または20のいずれかに記載の融合タンパク質 の前記カーゴの細胞内送達のための使用。
- 23.請求項15から17、または21のいずれかに記載の共有結合した化学的 複合体の前記カーゴの細胞内送達のための使用。
- 24.薬学的に有効な量の請求項1から14のいずれかに記載の融合タンパク質 を含む薬学的組成物。
- 25.薬学的に有効な量の請求項19または20のいずれかに記載の融合タンパ ク質を含む薬学的組成物。
- 26.薬学的に有効な量の請求項15から18、または21のいずれかに記載の 共有結合した化学的複合体を含む薬学的組成物。
- 27.次の: (a)JB106(配列番号:38)、(b)JB117(配列番号:59)、 (c)JB118(配列番号:60)、(d)JB119(配列番号:61)、 (e)JB120(配列番号:62)、および、(f)JB122(配列番号: 63)、からなる群より選択される融合タンパク質をコードするヌクレオチド配 列を含む、DNA分子。
- 28.融合タンパク質tat−VP16R.GF(配列番号:58)をコードす るヌクレオチド配列を含むDNA分子。
- 29.請求項27に記載のDNA分子であって、前記融合タンパク質をコードす るヌクレオチド配列が、発現制御配列に作動可能に連結している、DNA分子。
- 30.請求項28に記載のDNA分子であって、前記融合タンパク質をコードす るヌクレオチド配列が、発現制御配列に作動可能に連結している、DNA分子。
- 31.請求項29に記載のDNA分子で形質転換した単細胞性宿主。
- 32.請求項30に記載のDNA分子で形質転換した単細胞性宿主。
- 33.次の、 (a)JB106(配列番号:38)、(b)JB117(配列番号:59)、 (c)JB118(配列番号:60)、(d)JB119(配列番号:61)、 (e)JB120(配列番号:62)、および、(f)JB122(配列番号: 63)、からなる群より選択される融合タンパク質を生成する方法であって、 該方法が以下の工程: (a)請求項31に記載の形質転換した単細胞性宿主を培養する工程;および、 (b)該培養から融合タンパク質を回収する工程、を包含する、方法。
- 34.HIV tatタンパク質のアミノ酸47−58に続くHSV VP16 タンパク質のアミノ酸43−412からなる融合タンパク質を生成する方法であ って、 該方法が以下の工程: (a)請求項32に記載の形質転換した単細胞性宿主を培養する工程;および、 (b)該培養から融合タンパク質を回収する工程、を包含する、方法。
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JPH05505102A (ja) * | 1989-12-21 | 1993-08-05 | ホワイトヘツド・インスチチユート・フオー・バイオメデイカル・リサーチ | 真核細胞の中に分子を配達する方法 |
US5219990A (en) | 1991-01-28 | 1993-06-15 | Biogen, Inc. | Papillomavirus e2 trans-activation repressors |
-
1993
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- 1993-08-19 WO PCT/US1993/007833 patent/WO1994004686A1/en active IP Right Grant
- 1993-08-19 DE DE0656950T patent/DE656950T1/de active Pending
- 1993-08-19 DE DE69321962T patent/DE69321962T2/de not_active Expired - Lifetime
- 1993-08-19 CA CA002135642A patent/CA2135642C/en not_active Expired - Lifetime
- 1993-08-19 NZ NZ255831A patent/NZ255831A/en not_active IP Right Cessation
- 1993-08-19 DK DK93920231T patent/DK0656950T3/da active
- 1993-08-19 EP EP08004968A patent/EP2000536A3/en not_active Withdrawn
- 1993-08-19 EP EP98105625A patent/EP0903408A3/en not_active Ceased
- 1993-08-19 AT AT93920231T patent/ATE173016T1/de active
- 1993-08-19 AU AU50832/93A patent/AU667244B2/en not_active Expired
- 1993-08-19 EP EP93920231A patent/EP0656950B1/en not_active Expired - Lifetime
- 1993-08-19 JP JP6506542A patent/JP2702285B2/ja not_active Expired - Lifetime
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- 1994-11-09 NO NO19944273A patent/NO316761B1/no not_active IP Right Cessation
- 1994-12-28 KR KR1019940704779A patent/KR0153027B1/ko not_active IP Right Cessation
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1997
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2004513059A (ja) * | 1998-12-24 | 2004-04-30 | ユセベ,ソシエテ アノニム | ペプチド産物、方法及び組成物 |
JP2011155990A (ja) * | 1999-10-12 | 2011-08-18 | Xigen Sa | Jnkシグナル導入経路の細胞透過性ペプチドインヒビター |
US8183339B1 (en) | 1999-10-12 | 2012-05-22 | Xigen S.A. | Cell-permeable peptide inhibitors of the JNK signal transduction pathway |
US8236924B2 (en) | 1999-10-12 | 2012-08-07 | Xigen Sa | Cell-permeable peptide inhibitors of the JNK signal transduction pathway |
US8278413B2 (en) | 1999-10-12 | 2012-10-02 | Xigen Sa | Cell-permeable peptide inhibitors of the JNK signal transduction pathway |
JP2012097094A (ja) * | 2000-07-21 | 2012-05-24 | Revance Therapeutics Inc | 多成分生物学的輸送システム |
JP2007521332A (ja) * | 2003-12-12 | 2007-08-02 | クアンタム ドット コーポレーション | 生体膜を貫通する半導体ナノ結晶の輸送を向上させる方法 |
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EP2000536A3 (en) | 2010-06-30 |
CA2135642A1 (en) | 1994-03-03 |
AU5083293A (en) | 1994-03-15 |
DE656950T1 (de) | 1996-03-14 |
DE69321962D1 (de) | 1998-12-10 |
CA2135642C (en) | 1999-12-14 |
NZ255831A (en) | 1997-04-24 |
JP2702285B2 (ja) | 1998-01-21 |
EP0903408A2 (en) | 1999-03-24 |
AU667244B2 (en) | 1996-03-14 |
NO316761B1 (no) | 2004-05-03 |
DK0656950T3 (da) | 1999-07-19 |
EP2000536A2 (en) | 2008-12-10 |
FI120495B (fi) | 2009-11-13 |
ATE173016T1 (de) | 1998-11-15 |
ES2123062T3 (es) | 1999-01-01 |
KR0153027B1 (en) | 1998-10-15 |
JP2869396B2 (ja) | 1999-03-10 |
DE69321962T2 (de) | 1999-07-01 |
NO944273L (no) | 1995-02-17 |
NO944273D0 (no) | 1994-11-09 |
EP0656950A1 (en) | 1995-06-14 |
FI945248A0 (fi) | 1994-11-08 |
WO1994004686A1 (en) | 1994-03-03 |
EP0903408A3 (en) | 2005-11-02 |
FI945248A (fi) | 1995-01-05 |
JPH1033186A (ja) | 1998-02-10 |
HK1012678A1 (en) | 1999-08-06 |
EP0656950B1 (en) | 1998-11-04 |
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