JP4342934B2 - Pept−2輸送体を介した薬剤の投与 - Google Patents
Pept−2輸送体を介した薬剤の投与 Download PDFInfo
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- JP4342934B2 JP4342934B2 JP2003503004A JP2003503004A JP4342934B2 JP 4342934 B2 JP4342934 B2 JP 4342934B2 JP 2003503004 A JP2003503004 A JP 2003503004A JP 2003503004 A JP2003503004 A JP 2003503004A JP 4342934 B2 JP4342934 B2 JP 4342934B2
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- pept2
- conjugate
- transporter
- pept1
- drug
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Description
本出願は、2002年3月1日に出願された米国特許出願第60/361,002号および2001年6月11日に出願された米国特許出願第60/297,732号からの優先権に由来しており、これらは両方とも、全目的についてその全体が参照として本明細書に組み入れられる。
製薬産業における近年の発展により、多数の可能性ある治療薬が形成されるようになった。しかし、効果的な、経口的な生物学的利用能の化合物を製剤化することは、取り込みおよび代謝酵素に対する高感受性に関連した問題のために困難であることが判明している。
本発明は、PEPT2輸送体の基質である接合体部分に連結した薬学的薬剤を含む接合体を提供する。接合体のVmaxは、PEPT2輸送体に対するGly-Sarの少なくとも1%である。PEPT2に対する接合体のVmaxは、薬学的薬剤のみ、すなわち接合体部分を含まないものよりも大きい。
タンパク質に言及する場合の「特異的に結合する」または、抗体に言及する場合の「特異的に免疫反応する」という用語は、タンパク質および他の生物製剤の異種個体群の存在下におけるタンパク質の存在の決定因子である、結合反応を意味する。従って、指定した条件下で、特異的リガンドは特定のタンパク質に優先的に結合し、試料中に存在する他のタンパク質には有意な量では結合しない。タンパク質に特異的に結合する抗体などの分子の会合定数は、少なくとも106M-1または107M-1、好ましくは108M-1から109M-1、より好ましくは約1010M-1から1011M-1またはそれ以上であることが多い。しかし、輸送体の基質のいくつか、特にPEPT1は、10〜103M-1オーダーというはるかに低い親和性しか有さないが、結合は依然として特異的であると示すことができる。様々な免疫アッセイ形式を使用して、特定のタンパク質と特異的に免疫反応する抗体を選択できる。例えば、固相ELISA免疫アッセイを慣用的に使用して、タンパク質と特異的に免疫反応するモノクローナル抗体を選択する。特異的免疫反応性の決定に使用できる免疫アッセイ形式および条件の説明については、例えば、HarlowおよびLane(1988)「抗体、実験マニュアル(Antibodies, A Laboratory Manual)」、Cold Spring Harbor Publications、New Yorkを参照されたい。
1.序論
本発明は、PEPT2輸送体を介して基質として輸送されるべき容量について、薬剤、接合体、または、薬剤に連結したもしくは連結可能な接合体部分をスクリーニングする方法を提供する。本発明はまた、単独でもしくは接合体部分への連結の結果としてPEPT2輸送体の基質となる薬剤の経口送達を伴う治療法を提供する。本発明の方法は一部、ヒト腸、特に胃、空腸、回腸、回盲弁、盲腸、および上行結腸でPEPT2が発現されていることが示された、発明者らの結果を前提とする。以前の研究者の報告では、PEPT2は、脳および腎臓には存在するが、腸には存在しない。本発明の結果と以前の研究の間の矛盾は、PEPT2が発現されている組織を決定するための以前の研究の大半が、ヒトではなくラットで実施されていたこと、および、本発明の実施例に使用した定量的PCRの検出感度がずっと高いことに起因しうる。
ヒトPEPT1は、Liang、Journal of Biological Chemistry 270:6456-6463(1995)により、2263bpのcDNAとしてクローニングされ、これは、708アミノ酸のタンパク質をコードする2127bpのオープンリーディングフレームを有する。PEPT1への言及には、Liangのアミノ酸配列、その対立遺伝子、同族体、および誘導変種が含まれる。通常、このような変種は、Liangの例示的配列に対して少なくとも90%の配列同一性を示す。ヒトPEPT1配列の同族型は、ウサギおよびラット組織からクローニングされている。それぞれ、Fei、Nature 368:563-566(1994)、およびMiyamoto、Biochimica et Biophysica Acta 1305:34-38(1996)。
薬理活性を有することが知られているか、または疑われる薬剤を、PEPT2輸送体の基質として作用する容量について直接スクリーニングできる。または、接合体部分を基質としてスクリーニングでき、接合体部分は、薬理活性を有することが知られているか、または疑われる薬剤に連結している。このような方法において、接合体部分は、スクリーニング過程中に、接合体として薬剤または他の分子に連結できる。別の分子を使用する場合には、分子は、薬学的使用のために接合体部分に連結することが最終的に意図される薬剤の構造に似るように選択されることがある。スクリーニングは、典型的には、PEPT2輸送体を発現している細胞上で実施する。いくつかの方法では、細胞を、PEPT2輸送体をコードするDNAでトランスフェクトする。別の方法では、PEPT2輸送体を発現している天然細胞を使用する。いくつかの方法では、PEPT2は、発現されている唯一の輸送体であるかまたは唯一のペプチド輸送体である。別の方法では、細胞は、他の輸送体と組み合せてPEPT2を発現している。例えば、いくつかの方法では、PEPT1およびPEPT2の両方を発現している細胞を使用する。さらに別の方法では、薬剤、接合体、または接合体部分を、異なる輸送体を発現している異なる細胞上でスクリーニングする。例えば、薬剤または接合体は、PEPT2を発現している細胞上で、および、PEPT1を発現している細胞上でスクリーニングできる。輸送体を有する細胞を介した透過について薬剤、接合体、または接合体部分をスクリーニングする方法は、国際公開公報第01/20331号に記載されている。
スクリーニング対象となる薬剤、接合体、または接合体部分を構成する化合物は、天然分子でも合成分子でもよい。天然供給源には、例えば海洋微生物、藻、植物、および真菌などの供給源が含まれる。または、スクリーニング対象となる化合物は、ペプチドまたは小分子を含む薬剤のコンビナトリアルライブラリから、または、例えば化学産業、製薬産業、環境産業、農業産業、海洋産業、化粧品産業、薬品産業、およびバイオテクノロジー産業などの産業において合成される既存の化学的化合物のレパートリーに由来しうる。化合物には、例えば、医薬品、治療薬、環境物質、農薬、または産業品、汚染物質、化粧品、薬物、有機化合物、脂質、グルココルチコイド、抗体、ペプチド、糖、炭水化物、およびキメラ分子などが含まれる。
PEPT2または他の輸送体の基質である接合体部分を、様々な手段により、薬理活性を有する薬剤に付着させるまたは薬剤中に組み込むことができる。薬剤を接合体部分に直接接合すること(得られる共有結合はインビボで切断可能である)、または、薬剤と共に二官能基リンカー前駆体を接合体部分に共有結合的にカップリングすることのいずれかにより、本発明の接合体を調製できる。リンカー前駆体は、薬剤上の少なくとも1つの反応性官能基および接合体部分上の少なくとも1つの反応性官能基に相補的である少なくとも1つの反応性官能基を含むように選択される。このような相補的反応基は、下記に示したように、当技術分野において公知である。
相補的結合化学
それ自体がPEPT2の基質であるか、または、PEPT2の基質である接合体部分に連結している薬剤を、薬学的組成物に取り込むことができる。通常、必ずとは限らないが、このような薬学的組成物は経口投与用に設計されている。このような組成物の経口投与により、PEPT2を介して腸を通じて取り込まれ、全身循環系へと進入する。従って、薬学的組成物を、生体中の様々な組織に効率的に送達できる。PEPT2に対する組成物の特異性によって、組成物は、高レベルでPEPT2を発現している脳(脈絡叢を含む)および腎臓に取り込まれ易くなる。しかし、本方法はまた、PEPT2が有意な程度に発現されている脳、腎臓、肺、および脾臓の疾患を有さない患者における様々な疾病の治療にも有用である。このような方法において、腎臓におけるPEPT2の発現により、薬学的組成物の全身循環系への再吸収が増加し、これによりその半減期は増加して、よって必要な投与量が減少する。いくつかの方法において、薬剤または接合体部分は、PEPT2およびPEPT1の両方の基質である。いくつかの方法において、薬剤または接合体部分はPEPT2の基質であって、PEPT1の基質ではない、または不十分な基質である。
1.輸送体発現のPCR解析
ヒトPEPT1(GenBankを使用して2セット)またはPEPT2(GenBankを使用して2セット)中の特定の配列を増幅するために、オリゴヌクレオチドプライマーを設計した。正プライマー配列および逆プライマー配列は、以下であった
(3'UTRの147塩基対を増幅するPEPT1#1
(配列番号:1)および
(配列番号:2);終止コドンを横切り197塩基対を増幅するPEPT1#2
(配列番号:3)および
(配列番号:4);PEPT2オープンリーディングフレーム中の533塩基対を増幅するPEPT2#1
(配列番号:5)および
(配列番号:6);PEPT2オープンリーディングフレーム中の最後の376塩基対を増幅するPEPT2#2
(配列番号:7)および
(配列番号:8))。全てのプライマーのアニーリング温度が55℃を超えており、特異性を確認するために生成物をシークエンシングした。
GB# = GenBankアクセッション番号
Sto = 胃
Eso = 食道
Duo = 十二指腸
Jej = 空腸
Ile = 回腸
Il-Ce = 回腸−盲腸弁
Cec = 盲腸
Acol = 上行結腸
Tcol = 全結腸
Dcol = 下行結腸
Hea = 心臓
Bra = 脳
Lun = 肺
SMus = 平滑筋
Kid = 腎臓
Pan = 膵臓
Liv = 肝臓
thy = 胸腺
spl = 脾臓
Leu = 白血球
Pla = 血小板
Pros = 前立腺
test = 精巣
Ova = 卵巣
完全なオープンリーディングフレームを、アフリカツメガエル卵母細胞発現プラスミドにクローニングして直線化し、cRNAを、T7ポリメラーゼを使用した流出転写により作製した。アフリカツメガエル卵母細胞を調製し、前記(Collinsら、1997)されているように維持し、10ng〜30ngのRNAを注入した。輸送電流を、2電極電圧固定(Axon Instruments社)を使用して注入の2日〜4日後に測定した。全実験は、修飾した卵母細胞リンガー液(90mM NaCl、2mM KCl、1.8mM CaCl2、1mM MgCl2、および10mM NaHEPES、pH6.8)を使用して実施した。卵母細胞の膜電位を-60mVに保持し、PowerLabソフトウェアを使用して電流の軌跡を得た。化合物に対する応答を、PEPT1およびPEPT2に対する特定の非輸送阻害剤(XP10973)の存在下および非存在下で測定した。データは、XP10973により遮断される電流として表現する。
Caco-2細胞を、ミリポアトランスウェルフィルターに播種し、18日〜22日間分化させた。単層の完全性は、単層を横切る放射標識イヌリン輸送の消失により確認した。化合物を頂端チャンバーに加え、側底チャンバーにおける化合物の様子を、シンチレーション計測またはLC/MS/MSにより種々の時点において測定した。
21個の50mlアルテック(Alltech)チューブに、ポリスチレン-クロロトリチルクロリド樹脂(各5g)、ジクロロメタン(25mL)、ならびに3当量のFmoc-アミノ酸(構造については図3を参照されたい)、および6当量のジエチルイソプロピルアミンを加える。反応液を室温で30分間振とうする。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、およびN,N-ジメチルホルムアミド(3回)で洗浄する。その後、樹脂を20%ピペリジンを含むN,N-ジメチルホルムアミド溶液で1時間処理する。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、およびN,N-ジメチルホルムアミド(3回)で洗浄する。各樹脂を4つの25mlアルテックチューブに分割し、N,N-ジメチルホルムアミド(10mL)を加えた。各4つの異なるチューブに、5当量のBoc-Allocアミノ酸(図4)、5当量のHATU、および10当量のジエチルイソプロピルアミンの混合物を含む10mLのN,N-ジメチルホルムアミド溶液を加えた。反応液を周囲温度で20時間振とうする。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、およびN,N-ジメチルホルムアミド(3回)で洗浄する。各樹脂を、0.1当量のテトラキス(トリフェニルホスフィン)パラジウム(0)を含むN,N-ジメチルホルムアミド(10mL)溶液で20時間処理し、allocを脱保護する。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、およびN,N-ジメチルホルムアミド(3回)で洗浄する。各樹脂を、12個の4mLアルテックチューブに分割し、ジクロロメタン(1mL)を加えた。各12個の別々のチューブに、5当量のカルボン酸(図5)、5当量のHATU、および10当量のジエチルイソプロピルアミンの混合物を含む1mLのN,N-ジメチルホルムアミド溶液を加える。反応液を周囲温度で20時間振とうする。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、N,N-ジメチルホルムアミド(3回)、およびジクロロメタン(3回)で洗浄する。得られた1008個のチューブを、90%トリフルオロ酢酸を含むジクロロメタン(0.5mL)溶液で3時間処理し、チューブを12個の2mL深型96ウェルプレートに流す。溶媒を減圧下でGeneVacを使用して除去する。得られた残渣をDMSOに溶解させてほぼ100mMの濃度とし、生物学的アッセイに供して、PEPT2を介した輸送容量について試験した(例えば、前述のようなPEPT2でトランスフェクトした卵母細胞を使用して)。
4個の250mLのペプチド容器に、ポリスチレン-クロロトリチルクロリド樹脂(各20g)、ジクロロメタン125mL、ならびに3当量のFmoc-alloc-アミノ酸(構造については図6を参照されたい)、および6当量のジエチルイソプロピルアミンを加える。反応液を周囲温度で30分間振とうする。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、およびN,N-ジメチルホルムアミド(3回)で洗浄する。その後、樹脂を20%ピペリジンを含むN,N-ジメチルホルムアミド溶液で1時間処理する。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、およびN,N-ジメチルホルムアミド(3回)で洗浄する。各樹脂を21個の25mLアルテックチューブに分割し、N,N-ジメチルホルムアミド(10mL)を加える。4つの別々のチューブそれぞれに、5当量のBoc-アミノ酸(図7)、5当量のHATU、および10当量のジエチルイソプロピルアミンの混合物を含む10mLのN,N-ジメチルホルムアミド溶液を加える。反応液を周囲温度で20時間振とうする。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、およびN,N-ジメチルホルムアミド(3回)で洗浄する。各樹脂を、0.1当量のテトラキス(トリフェニルホスフィン)パラジウム(0)を含むN,N-ジメチルホルムアミド(10mL)溶液で20時間処理し、alloc脱保護を行なう。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、およびN,N-ジメチルホルムアミド(3回)で洗浄する。各樹脂を12個の4mLアルテックチューブに分割し、ジクロロメタン(1mL)を加えた。12個の別々のチューブそれぞれに、5当量のカルボン酸(図5)、5当量のHATU、および10当量のジエチルイソプロピルアミンの混合物を含む1mLのN,N-ジメチルホルムアミド溶液を加える。反応液を周囲温度で20時間振とうする。樹脂を流し、メタノール(2回)、ジクロロメタン(3回)、N,N-ジメチルホルムアミド(3回)、およびジクロロメタン(3回)で洗浄する。得られた1008個のチューブを90%トリフルオロ酢酸を含むジクロロメタン(0.5ml)溶液で3時間処理し、チューブを11個の2mL深型96ウェルプレートに流した。溶媒を減圧下でGeneVacを使用して除去する。得られた残渣をDMSOに溶解させてほぼ100mMの濃度とし、生物学的アッセイに供して、PEPT2を介した輸送容量について試験した(例えば、前述のようなPEPT2でトランスフェクトした卵母細胞を使用して)。
Claims (5)
- ヒト腸組織におけるヒトPEPT2輸送体を介した輸送について薬剤、接合体、または接合体部分をスクリーニングする方法であって、以下の段階を含む方法:
ヒトPEPT2輸送体を発現する細胞を提供する段階;
細胞を薬剤、接合体、または接合体部分と接触させる段階;ならびに
薬剤、接合体、または接合体部分が、輸送体によって細胞中に入るかどうか、および/または細胞を透過するかどうかを判定する段階。 - 細胞を、ヒトPEPT2輸送体をコードするDNAでトランスフェクトする、請求項1記載の方法。
- 細胞が、検出可能なヒトPEPT1輸送体を全く有さない、請求項1記載の方法。
- ヒトPEPT1輸送体を発現しかつヒトPEPT2輸送体を欠失している第二細胞を提供する段階;
細胞を、薬剤、接合体、または接合体部分と接触させる段階;および
薬剤、接合体、または接合体部分がPEPT1輸送体によって細胞中に入るかどうか、および/または細胞を透過するかどうかを判定する段階
をさらに含む、請求項1記載の方法。 - 薬剤、接合体、または接合体部分が、ヒトPEPT1輸送体ではなくヒトPEPT2輸送体によって輸送される、請求項1記載の方法。
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-
2002
- 2002-06-11 EP EP02746512A patent/EP1406493A4/en not_active Withdrawn
- 2002-06-11 JP JP2003503004A patent/JP4342934B2/ja not_active Expired - Fee Related
- 2002-06-11 US US10/170,217 patent/US6955888B2/en not_active Expired - Fee Related
- 2002-06-11 WO PCT/US2002/018686 patent/WO2002100172A1/en active Application Filing
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2005
- 2005-05-20 US US11/134,728 patent/US7507546B2/en not_active Expired - Fee Related
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US20090306036A1 (en) | 2009-12-10 |
US20030017964A1 (en) | 2003-01-23 |
JP2005501010A (ja) | 2005-01-13 |
US20050214853A1 (en) | 2005-09-29 |
US6955888B2 (en) | 2005-10-18 |
WO2002100172A1 (en) | 2002-12-19 |
EP1406493A1 (en) | 2004-04-14 |
EP1406493A4 (en) | 2006-06-14 |
US7507546B2 (en) | 2009-03-24 |
US7919454B2 (en) | 2011-04-05 |
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