JPH08511525A - Hiv伝播の合成ペプチド抑制物質 - Google Patents
Hiv伝播の合成ペプチド抑制物質Info
- Publication number
- JPH08511525A JPH08511525A JP7501831A JP50183195A JPH08511525A JP H08511525 A JPH08511525 A JP H08511525A JP 7501831 A JP7501831 A JP 7501831A JP 50183195 A JP50183195 A JP 50183195A JP H08511525 A JPH08511525 A JP H08511525A
- Authority
- JP
- Japan
- Prior art keywords
- virus
- peptide
- group
- hiv
- amino acid
- 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
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Classifications
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.ウイルスエンベロープタンパク質の細胞外ドメインのαヘリックス領域に対 応するアミノ酸配列を有するペプチドであって、高次コイル構造を有するロイシ ンジッパードメインを含む該ウイルスエンベロープタンパク質の第2のαヘリッ クス領域と相互作用してそれに結合する上記ペプチド。 2.前記ペプチドがALLMOTI5モチーフ、107x178x4モチーフまたはPLZIPモチーフ を用いるコンピュータによるペプチド配列検索により認識されるものである、請 求項1に記載のペプチド。 3.エンベロープを有するウイルスがレトロウイルスである、請求項1に記載の ペプチド。 4.レトロウイルスがヒトレトロウイルスである、請求項3に記載のペプチド。 5.ヒトレトロウイルスがHIV−1またはHIV−2である、請求項4に記載 のペプチド。 6.ヒトレトロウイルスがHTLV−IまたはHTLV−IIである、請求項4に 記載のペプチド。 7.エンベロープを有するウイルスが非ヒトレトロウイルスである、請求項1に 記載のペプチド。 8.非ヒトレトロウイルスがウシ白血症ウイルス、ネコ肉腫ウイルス、ネコ白血 病ウイルス、サル免疫不全ウイルス、サル肉腫ウイルスまたはヒツジ進行性肺炎 ウイルスである、請求項6に記載のペプチド。 9.エンベロープを有するウイルスがレトロウイルス以外のウイル スである、請求項1に記載のペプチド。 10.前記ウイルスがRS(respiratory syncytial)ウイルス、インフルエンザ ウイルス、パラインフルエンザウイルス、イヌジステンパーウイルスまたはニュ ーカッスル病ウイルスである、請求項9に記載のペプチド。 11.次式: (式中、 アミノ酸残基は一文字表記で表してあり、 Xはアミノ基、アセチル基、9−フルオレニルメトキシ−カルボニル基、 疎水基または巨大分子担体グループを含み、 Zはカルボキシル基、アミド基、疎水基または巨大分子担体グループを含 む) よりなる群から選ばれる式を有するペプチド。 12.次式: (式中、 アミノ酸残基は一文字表記で表してあり、 Xはアミノ基、アセチル基、9−フルオレニルメトキシ−カルボニル基、 疎水基または巨大分子担体グループを含み、 Zはカルボキシル基、アミド基、疎水基または巨大分子担体グループを含 む) よりなる群から選ばれる式を有するペプチド。 13.次式: (式中、 アミノ酸残基は一文字表記で表してあり、 Xはアミノ基、アセチル基、9−フルオレニルメトキシ−カルボニル基、 疎水基または巨大分子担体グループを含み、 Zはカルボキシル基、アミド基、疎水基または巨大分子担体グループを含 む) よりなる群から選ばれる式を有するペプチド。 14.次式: (式中、 アミノ酸残基は一文字表記で表してあり、 Xはアミノ基、アセチル基、9−フルオレニルメトキシ−カルボニル基、 疎水基または巨大分子担体グループを含み、 Zはカルボキシル基、アミド基、疎水基または巨大分子担体グループを含 む) よりなる群から選ばれる式を有するペプチド。 15.次式: (式中、 アミノ酸残基は一文字表記で表してあり、 Xはアミノ基、アセチル基、9−フルオレニルメトキシ−カルボニル基、 疎水基または巨大分子担体グループを含み、 Zはカルボキシル基、アミド基、疎水基または巨大分子担体グループを含 む) よりなる群から選ばれる式を有するペプチド。 16.次式: (式中、 アミノ酸残基は一文字表記で表してあり、 Xはアミノ基、アセチル基、9−フルオレニルメトキシ−カルボニル基、 疎水基または巨大分子担体グループを含み、 Zはカルボキシル基、アミド基、疎水基または巨大分子担体グループを含 む) よりなる群から選ばれる式を有するペプチド。 17.Xが疎水基である、請求項11、12、13、14、15または16に記載のペプチド。 18.疎水基Xがカルボベンゾキシル、ダンシルまたはt−ブチルオキシカルボニ ルである、請求項17に記載のペプチド。 19.Zが疎水基である、請求項11、12、13、14、15または16に記載のペプチド。 20.疎水基Zがt−ブチルオキシカルボニルである、請求項19に記載のペプチド 。 21.Xが巨大分子担体グループである、請求項11、12、13、14、15または16に記 載のペプチド。 22.巨大分子担体グループが脂質−脂肪酸結合体、ポリエチレングリコールまた は炭水化物成分である、請求項21に記載のペプチド。 23.Zが巨大分子担体グループである、請求項11、12、13、14、15または16に記 載のペプチド。 24.巨大分子担体グループZが脂質−脂肪酸結合体、ポリエチレングリコールま たは炭水化物成分である、請求項23に記載のペプチド。 25.隣接アミノ酸残基を連結している少なくとも1つの結合が非ペプチド結合で ある、請求項11、12、13、14、15または16に記載のペプチド。 26.非ペプチド結合がイミノ、エステル、ヒドラジン、セミカルバジドまたはア ゾ結合である、請求項25に記載のペプチド。 27.少なくとも1個のアミノ酸残基がD異性体の配置にある、請求項11、12、13 、14、15または16に記載のペプチド。 28.少なくとも1個のアミノ酸の挿入をさらに含む、請求項11、12、13、14、15 または16に記載のペプチド。 29.アミノ酸の挿入が1〜15個のアミノ酸残基である、請求項11、12、13、14 、15または16に記載のペプチド。 30.アミノ酸残基がアミノ酸の欠失を表し、前記ペプチドが少なくとも3個のア ミノ酸残基を含んでなる、少なくとも1個少ないアミノ酸残基を有する請求項11 、12、13、14、15または16に記載のペプチド。 31.第1のアミノ酸残基が第2の異なるアミノ酸残基で置換される少なくとも1 個のアミノ酸の置換をさらに含む、請求項11、12、13、14、15または16に記載の ペプチド。 32.アミノ酸の置換が保存的置換である、請求項31に記載のペプチド。 33.アミノ酸の置換が非保存的置換である、請求項31に記載のペプチド。 34.エンベロープを有するウイルスの細胞への伝播を抑制する方法であって、細 胞と有効濃度の請求項1のペプチドとを効果的な期間にわたり接触させて、該ウ イルスによる細胞の感染が起こらないようにすることを含んでなる上記方法。 35.宿主内のエンベロープを有するウイルスを中和する方法であって、宿主に有 効濃度の請求項1のペプチドを投与して、宿主において該ウイルスを中和するの に十分な免疫応答を引き出し、かつ宿主の未感染細胞のウイルス感染を抑制する ようにすることを含んでなる上記方法。 36.宿主内のエンベロープを有するウイルスを中和する方法であって、宿主に、 有効濃度の請求項1のペプチドに対する抗体を投与して、宿主内の未感染細胞の ウイルス感染を抑制するようにすることを含んでなる上記方法。 37.エンベロープを有するウイルスの検出方法であって、 ウイルス単離物と有効濃度の請求項1のペプチドとを効果的な期間にわたり 接触させてウイルスの感染性を抑制し、そして ウイルスの酵素活性について該ウイルス単離物をアッセイする、ことを含ん でなる上記方法。 38.HIVレトロウイルスの細胞への伝播を抑制する方法であって、細胞と有効 濃度の請求項11または12のペプチドとを効果的な期間にわたり接触させることに より、該レトロウイルスによる細胞の 感染が起こらないようにすることを含んでなる上記方法。 39.宿主内のHIVレトロウイルスを中和する方法であって、宿主に、有効濃度 の請求項11または12のペプチドを投与して、宿主においてHIVレトロウイルス を中和するのに十分な免疫応答を引き出し、かつ宿主内の未感染細胞のHIV感 染を抑制するようにすることを含んでなる上記方法。 40.宿主内のHIVレトロウイルスを中和する方法であって、宿主に、有効濃度 の請求項11または12のペプチドに対する抗体を投与して、宿主内の未感染細胞の HIV感染を抑制するようにすることを含んでなる上記方法。 41.HIVを検出する方法であって、 ウイルス単離物と有効濃度の請求項11または12のペプチドとを効果的な期間 にわたり接触させてHIVウイルスの感染性を抑制し、そして レトロウイルスの酵素活性について該ウイルス単離物をアッセイする、 ことを含んでなる上記方法。 42.RS(respiratory syncytial)ウイルスの細胞への伝播を抑制する方法で あって、細胞と有効濃度の請求項13または14のペプチドとを効果的な期間にわた り接触させることにより、該ウイルスによる細胞の感染が起こらないようにする ことを含んでなる上記方法。 43.宿主内のRSウイルスを中和する方法であって、宿主に、有効濃度の請求項 13または14のペプチドを投与して、宿主において該ウイルスを中和するのに十分 な免疫応答を引き出し、かつ宿主内 の未感染細胞のRSウイルス感染を抑制するようにすることを含んでなる上記方 法。 44.宿主内のRSウイルスを中和する方法であって、宿主に、有効濃度の請求項 13または14のペプチドに対する抗体を投与して、宿主内の未感染細胞のRSウイ ルス感染を抑制するようにすることを含んでなる上記方法。 45.RSウイルスを検出する方法であって、 ウイルス単離物と有効濃度の請求項13または14のペプチドとを効果的な期間 にわたり接触させてRSウイルスの感染性を抑制し、そして RSウイルスの酵素活性について該ウイルス単離物をアッセイする、 ことを含んでなる上記方法。 46.パラインフルエンザウイルスの細胞への伝播を抑制する方法であって、細胞 と有効濃度の請求項15または16のペプチドとを効果的な期間にわたり接触させる ことにより、該ウイルスによる細胞の感染が起こらないようにすることを含んで なる上記方法。 47.宿主内のパラインフルエンザウイルスを中和する方法であって、宿主に、有 効濃度の請求項15または16のペプチドを投与して、宿主において該ウイルスを中 和するのに十分な免疫応答を引き出し、かつ宿主内の未感染細胞のパラインフル エンザ感染を抑制するようにすることを含んでなる上記方法。 48.宿主内のパラインフルエンザウイルスを中和する方法であって、宿主に、有 効濃度の請求項15または16のペプチドに対する抗体を投与して、宿主内の未感染 細胞のパラインフルエンザ感染を抑制 するようにすることを含んでなる上記方法。 49.パラインフルエンザウイルスを検出する方法であって、 ウイルス単離物と有効濃度の請求項15または16のペプチドとを効果的な期間 にわたり接触させてパラインフルエンザウイルスの感染性を抑制し、そして パラインフルエンザウイルスの酵素活性について該ウイルス単離物をアッセ イする、 ことを含んでなる上記方法。
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JP2003504344A (ja) * | 1999-07-09 | 2003-02-04 | トリメリス,インコーポレーテッド | 増強された薬物動態学的性質をもつハイブリッドポリペプチド |
JP2003522948A (ja) * | 2000-02-10 | 2003-07-29 | パナコス ファーマシューティカルズ, インコーポレイテッド | ウイルス融合インヒビターの検出のための分析 |
WO2008050830A1 (fr) * | 2006-10-25 | 2008-05-02 | Kyoto University | Agent anti-vih |
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US6440656B1 (en) | 2002-08-27 |
NZ329775A (en) | 2000-05-26 |
NZ501727A (en) | 2002-07-26 |
US7514397B1 (en) | 2009-04-07 |
EP1595890A3 (en) | 2007-03-21 |
AU692777B2 (en) | 1998-06-18 |
ATE293127T1 (de) | 2005-04-15 |
CL2009002139A1 (es) | 2010-05-07 |
EP0774971A4 (en) | 1998-06-10 |
EP0774971A1 (en) | 1997-05-28 |
JP4205159B2 (ja) | 2009-01-07 |
CA2164698A1 (en) | 1994-12-22 |
ES2238674T3 (es) | 2005-09-01 |
KR100355407B1 (ko) | 2003-02-07 |
NL300192I2 (nl) | 2005-08-01 |
NL300192I1 (nl) | 2005-07-01 |
DE122005000025I2 (de) | 2006-02-09 |
NZ267803A (en) | 1999-03-29 |
KR960702753A (ko) | 1996-05-23 |
DE69434335T2 (de) | 2006-02-16 |
PT774971E (pt) | 2005-07-29 |
DE122005000025I1 (de) | 2005-08-04 |
CA2164698C (en) | 2012-10-09 |
AU7042694A (en) | 1995-01-03 |
EP0774971B1 (en) | 2005-04-13 |
EP1595890A2 (en) | 2005-11-16 |
WO1994028920A1 (en) | 1994-12-22 |
US5464933A (en) | 1995-11-07 |
US6133418A (en) | 2000-10-17 |
DK0774971T3 (da) | 2005-08-22 |
DE69434335D1 (de) | 2005-05-19 |
LU91166I2 (fr) | 2005-06-20 |
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