JP5724937B2 - 腎臓集積性を示すペプチド、製剤 - Google Patents
腎臓集積性を示すペプチド、製剤 Download PDFInfo
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- JP5724937B2 JP5724937B2 JP2012097763A JP2012097763A JP5724937B2 JP 5724937 B2 JP5724937 B2 JP 5724937B2 JP 2012097763 A JP2012097763 A JP 2012097763A JP 2012097763 A JP2012097763 A JP 2012097763A JP 5724937 B2 JP5724937 B2 JP 5724937B2
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- kidney
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Landscapes
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Description
本発明で使用される薬物担体の具体例は、ウイルスベクター(レトロウイルスベクター、AAVベクター及びそれらの改変体又は化学修飾体)、アルブミン、天然高分子、合成高分子、リポソーム、エマルション、ミセル、マイクロスフェア、又はナノスフェアであるが、薬物の化学的及び物理的性質に影響を与えないものであって、薬物の輸送手段として適用できるものであれば特に限定されない。
表面にCys-Xaa-Cysのランダムなペプチド配列を提示するファージは、当該ランダム配列をfUSE5ベクターに挿入することによって作製された。Xaaは、19種類の通常のアミノ酸を意味する。
Wistar雄性ラット(6週齢、体重170g〜200g)にペントバルビタール麻酔下、Cys-Xaa-Cysファージ1010TUを尾静注した。15分後、心臓からPBSを還流させることで全身を脱血し、その後腎臓を摘出した。摘出された腎臓は、Lysis buffer中で腎皮膜を剥離された後、重量を測定された。その後、腎皮膜を剥離された腎臓をホモジナイズし、得られた腎ホモジネート液を遠心した(2000rpm、4℃、10分間)。さらに、その上清を超遠心分離機にかけた(55000rpm,4℃,13分間)。得られたペレットを、腎臓集積性ファージとした。
回収されたファージのペプチド配列は、ABI310 genetic analyzerを用いて解析された。
(1)コロニー数による評価試験
Wistar雄性ラット(6週齢、170g〜200g)にペントバルビタール麻酔下、ファージディスプレイ法によるスクリーニングで絞られた5種類のペプチド(アミノ酸1文字表記でC-ILASGVT-C、C-HGVQARL-C、C-RIGGMSN-C、C-SSYSSVT-C及びC-VMATGGV-C/すなわち、配列番号:1〜5に示されるペプチド)を提示した各々のファージを、PBSに溶解させ、1010TUを尾静注した。15分後、ペリスタポンプを用いて42℃のPBS-tween0.05%を還流させることにより全身脱血し、各臓器を摘出した。摘出された臓器を、Lysis buffer中で洗浄した後、重量を測定した。その後、ホモジナイズにより各臓器のホモジネート液を得ることにより、各臓器に集積したファージを回収した。
上記(1)の評価試験により、最も腎臓に対する集積性が認められたC-HGVQARL-C(配列番号:2に示されるペプチド)と、腎臓への集積性が認められなかったC-SSYSSVT-C(配列番号:4に示されるペプチド)の両ペプチドのN末端にFITCを結合させたペプチド(FITC標識ペプチド、純度90%)をべックス社に委託して合成した。配列番号:2及び4のペプチドは、ペプチド合成機(島津製作所、PSSM-8)を用いて合成された。
Claims (2)
- 配列番号:2,3又は5のいずれかに示されるアミノ酸配列を有するペプチド。
- 請求項1に記載のペプチドと薬物とが化学的に結合した製剤。
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