JP4067516B2 - ランダムフラグメント化および再組立によるdna変異誘発 - Google Patents
ランダムフラグメント化および再組立によるdna変異誘発 Download PDFInfo
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Description
本明細書で使用される以下の用語は、以下の意味を有する:
用語「DNA再組立」は、同一の配列の間で組換えが生じる場合に使用される。
Health, Bethesda, MD) (1987);およびTramontanoら (1990) J.Mol.Biol.215:175)としてもまた知られる。可変領域のドメインは、代表的に、天然に存在する免疫グロブリン鎖のアミノ末端の約105〜115アミノ酸(例えば、アミノ酸1〜110)を含むが、いくらか短いまたは長い可変ドメインはもまた、単鎖抗体の形成に適している。
核酸再編成は、インビトロまたはインビボにおいて核酸フラグメントまたはポリヌクレオチドのプールを相同組換えする方法である。関連核酸配列またはポリヌクレオチドの混合物をランダムにフラグメント化し、そして再組立して、組換え核酸分子またはポリヌクレオチドのライブラリーまたは混合集団を生じる。
本発明のDNA再編成方法は、未知の配列のプール上で盲目的に実施され得る。再組立の混合オリゴヌクレオチド(再組立される配列に相同である末端を有する)を添加することにより、任意の配列混合物が任意の特定位置で別の配列混合物中に取り込まれ得る。従って、合成オリゴヌクレオチド、PCRフラグメント、または全遺伝子の混合物が、規定の位置で別の配列ライブラリーへ混合され得る。1つの配列(混合物)の挿入は、鋳型の別の部分における配列の挿入から独立する。従って、組換えの程度、要求される相同性の程度、およびライブラリーの多様性の程度は、再組立されるDNAの長さに従って独立してまたは同時に変化され得る。
同等のいくつかの標準的な遺伝子交配もまた、インビトロにおける再編成により実施され得る。例えば、「分子戻し交雑」は、目的の変異について選択しながら、変異体の核酸と野生型核酸との混合を反復することにより実施され得る。従来の育種におけるように、このアプローチは異なる供給源に由来する表現型を選択されたバックグランドに組み合わせるために使用され得る。これは、例えば、選択されない特徴(すなわち、免疫原性)に影響する中立変異を除去するために有用である。従って、このアプローチは、タンパク質におけるどの変異が増強される生物学的活性に関連するか関連しないかを決定するために有用であり得、誤りがちな変異誘発方法またはカセット変異誘発方法により達成され得ない利点を決定するために有用であり得る。
インビボにおける再編成の1つの実施態様において、特定核酸配列の混合集団は、各宿主細胞において、少なくとも2つの異なる核酸配列が存在する条件下で、細菌細胞または真核細胞へ導入される。フラグメントは種々の異なる方法により、宿主細胞へ導入され得る。宿主細胞は、当業者に公知の方法(例えば、塩化カルシウムを用いる処理)を使用してフラグメントで形質転換され得る。フラグメントがファージゲノムに挿入される場合、宿主細胞は特定核酸配列を有する組換えファージゲノムを用いてトランスフェクトされ得る。あるいは、核酸配列は、エレクトロポレーション、トランスフェクション、リポフェクション、バイオリスティック(biolistic)、接合などを用いて宿主細胞へ導入され得る。
本発明のインビボにおける組換え方法は、未知の変異体のプールまたは特定核酸フラグメントまたは配列の対立遺伝子上で盲目的に実施され得る。しかし、特定核酸フラグメントの実際のDNAまたはRNA配列を知る必要はない。
本方法は、開示された方法のいずれかによるインビトロおよび/またはインビボにおける組換えにより、および任意の組み合わせで、ペプチドディスプレイ法により選択されるポリヌクレオチド配列を再編成するために使用され得、ここでは会合されたポリヌクレオチドは、表現型(例えば、予め決定されたレセプター(リガンド)に対するアフィニティーについて)についてスクリーニングされるディスプレイされたペプチドをコードする。
本発明の方法は、開示された方法のいずれかによるインビトロおよび/またはインビボ組換えおよび任意の組み合わせにより、抗体ディスプレイ法により選択されたポリヌクレオチド配列を再編成するために用いられ得る。ここで会合されたポリヌクレオチドは、表現型(例えば、予め決定された抗原(リガンド)への結合についてのアフィニティー)についてスクリーニングされたディスプレイされた抗体をコードする。
88: 10134;Hoogenboomら、(1991) Nucleic Acids Res.19: 4133;Changら、(1991) J.Immunol.147: 3610;Breitlingら、(1991)
Gene 104: 147;Marksら、(1991) J.Mol.Biol.222: 581;Barbasら、(1992) Proc.Natl.Acad.Sci.(U.S.A.) 89: 4457;HawkinsおよびWinter (1992) J.Immunol.22: 867; Marksら、(1992) Biotechnology 10: 779;Marksら、(1992) J.Biol.Chem.267: 16007; Lowmanら、(1991) Biochemistry 30: 10832;Lernerら、(1992) Science 258: 1313は、参考として本明細書中に援用される)。代表的には、バクテリオファージ抗体ディスプレイライブラリーは、固定化(例えば、アフィニティークロマトグラフィーにより反応性ファージについて富化するためのクロマトグラフィー樹脂への共有結合による)および/または標識(例えば、プラークまたはコロニーリフトをスクリーニングするために)されているレセプター(例えば、ポリペプチド、炭水化物、糖タンパク質、核酸)でスクリーニングされる。
581;Chaudharyら、(1990) Proc.Natl.Acad.Sci.(USA) 87: 1066;Chiswellら、(1992) TIBTECH 10: 80;McCaffertyら、(1990) 前出;およびHustonら、(1988) Proc.Natl.Acad.Sci.(USA) 85: 5879)。バクテリオファージコートタンパク質においてディスプレイされるscFvライブラリーの種々の実施様態が記載されている。
mutagenesis)により、それ自身多様化させられ得る。代表的には、VHおよびVLカセットは、相補性決定領域(CDR)(しばしば第3のCDR、CDR3)内またはその近くにおいて多様化される。酵素的インバースPCR変異誘発は、誤りがちなPCRおよび化学的変異誘発がそうであるように(Dengら、(1994) J.Biol.Chem.269:9533)、scFv部位特異的変異体の比較的大きなライブラリーを構築することに関して単純かつ信頼し得る方法であることが示されている(Stemmerら、(1993)
Biotechniques 14: 256)。Riechmannら、(1993) Biochemistry 32: 8848は、縮重オリゴヌクレオチドPCRおよび引き続いて結果として生じるscFv変異体のファージディスプレイによる部位特異的ランダム化を用いる抗体scFvフラグメントの半合理的な設計を示した。Barbasら、(1992) 前出は、ヒト破傷風トキソイド結合Fabの合成CDR領域における配列をランダム化することにより、偏った可変領域配列を用いることに起因する制限されたレパートリーサイズの問題を回避することを試みた。
M-1のアフィニティーで、好ましくは少なくとも約5×107 M-1のアフィニティーで、より好ましくは少なくとも1×108 M-1〜1×109 M-1またはそれ以上のアフィニティーで、ときには1×1010 M-1またはそれ以上のアフィニティーで、予め決定された抗原(例えば、免疫原)に結合する。頻繁には、予め決定された抗原は、例えばヒト細胞表面抗原(例えば、CD4、CD8、IL−2レセプター、EGFレセプター、PDGFレセプター)のようなヒトタンパク質、他のヒト生体高分子(例えば、トロンボモジュリン、プロテインC、糖質抗原、シアリルLewis抗原、L−セレクチン)、または非ヒト疾患関連高分子(例えば、細菌LPS、ビリオンカプシドタンパク質、またはエンベロープ糖タンパク質)などである。
Johnson SおよびBird RE (1991) Methods Enzymol.203: 88)。さらに、単鎖抗体は、抗体全体またはその種々のフラグメントを構築する基礎として用いられ得る(Kettleboroughら、(1994) Eur.J.Immunol.24: 952)。可変領域をコードする配列は、単離され得(例えば、PCR増幅またはサブクローン化により)、そして免疫原性が好適に最小化されるヒトの治療的使用により適切なヒト配列抗体をコードするように、所望のヒト定常領域をコードする配列にスプライシングされ得る。結果として生じる完全なヒトコード配列(1つまたは複数)を有するポリヌクレオチド(1つまたは複数)は、宿主細胞において発現され(例えば、哺乳動物細胞において発現ベクターから)、そして製薬製造のために精製され得る。
再編成はまたは、予め決定されたポリペプチド配列に結合するライブラリーメンバーを同定するためのツーハイブリッドスクリーニングシステムをスクリーニングすることにより得られた選択されたライブラリーメンバーのプールを組換え的に多様化するために用いられ得る。選択されたライブラリーメンバーは、プールされ、そしてインビトロおよび/またはインビボ組換えにより再編成される。次いで再編成されたプールは、前記の予め決定されたポリペプチド配列(例えば、SH2ドメイン)に結合するライブラリーメンバー、または別の予め決定されたポリペプチド配列(例えば、他のタンパク質の種由来のSH2ドメイン)を選択するために、酵母ツーハイブリッドシステムにおいてスクリーニングされ得る。
FASEB J.7: 957; Laloら、(1993) Proc.Natl.Acad.Sci.(USA) 90: 5524; Jacksonら、(1993) Mol.Cell.Biol.13; 2899;およびMaduraら、(1993) J.Biol.Chem.268: 12046)。ツーハイブリッドシステムはまた、2つの公知のタンパク質の相互作用する構造ドメインを同定するため(Bardwellら、(1993) Med.Microbiol.8: 1177; Chakrabortyら、(1992) J.Biol.Chem.267: 17498; Staudingerら、(1993) J.Biol.Chem.268: 4608; およびMilne GTおよびWeaver DT (1993) Genes Devel.7; 1755)、または単一のタンパク質のオリゴマー形成に機能するドメインを同定するためにも用いられている(Iwabuchiら、(1993) Oncogene 8; 1693; Bogerdら、(1993) J.Virol.67: 5030)。ツーハイブリッドシステムの変法は、タンパク質分解酵素のインビボでの活性を研究するために用いられている(Dasmahapatraら、(1992) Proc.Natl.Acad.Sci.(USA) 89: 4159)。あるいは、E.coli/BCCP 相互作用的スクリーニングシステム(Germinoら、(1993) Proc.Natl.Acad.Sci.(U.S.A.) 90: 933; Guarente L (1993) Proc.Natl.Acad.Sci.(U.S.A.) 90: 1639)は、相互作用するタンパク質配列(すなわち、ヘテロ二量体化するか、またはより高次のヘテロ多量体を形成するタンパク質配列)を同定するために用いられ得る。ツーハイブリッドシステムにより選択された配列は、プールおよび再編成され、そして予め決定された結合配列を含有するハイブリッドに結合するポリペプチド配列を同定するためのスクリーニングの1つ以上の引き続くラウンドのために、ツーハイブリッドシステムに導入され得る。このようにして同定された配列は、コンセンサス配列およびコンセンサス配列カーネルを同定するために比較され得る。
μl = マイクロリットル
μM = マイクロモル濃度
nM = ナノモル濃度
PBS = リン酸緩衝生理食塩水
ng = ナノグラム
μg = マイクログラム
IPTG = イソプロピルチオ−β−D−ガラクトシド
bp = 塩基対
kb = キロ塩基対
dNTP = デオキシヌクレオシド3リン酸
PCR = ポリメラーゼ連鎖反応
X−gal = 5−ブロモ−4−クロロ−3−インドリル−β−D−ガラクトシド
DNAseI= デオキシリボヌクレアーゼ
PBS = リン酸緩衝生理食塩水
CDR = 相補性決定領域
MIC = 最小阻止濃度
scFv = 抗体の単鎖Fvフラグメント
一般に、組換えDNA工学の標準的な技術は、種々の出版物(例えば、Sambrookら、1989, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory; Ausubelら、1987, Current Protocols in Molecular Biology、1巻および2巻ならびに増補、ならびにBergerおよびKimmel、Methods in Enzymology, Volume 152, Guide to Molecular Cloning Techniques (1987),
Academic Press, Inc., San Diego, CA、それぞれ参考として全体が本明細書中に援用される)に記載されている。制限酵素およびポリヌクレオチド修飾酵素を、製造業者の推奨に従って用いた。オリゴヌクレオチドをApplied Biosystems Inc.Model
394 DNA合成機で、ABIの化学製品を用いて合成した。所望であれば、予め決定されたDNA配列を増幅するためのPCRアンプリマー(amplimer)は、従事者の判断で選択され得る。
(1)基質の調製)
再組立反応のための基質は、pUC18由来の野生型LacZα遺伝子のdsDNAポリメラーゼ連鎖反応(「PCR」)産物であった(図2)(28; Gene Bank第XO2514号)。プライマー配列は、5’AAAGCGTCGATTTTTGTGAT3’(配列番号1)および5’ATGGGGTTCCGCGCACATTT3’(配列番号2)であった。遊離したプライマーを、製造業者の指示に従い、Wizard PCR prep(Promega, Madison WI)によりPCR産物から除去した。遊離したプライマーの除去は、重要であることが見い出された。
約5μgのDNA基質を、10〜20分間室温にて、100μlの[50mM
Tris−HCl pH 7.4, 1mM MgCl2]中で、0.15単位のDNAseI(Sigma, St.Louis MO)で消化した。消化されたDNAを、2%低融点アガロースゲルで泳動した。10〜70塩基対(bp)のフラグメントを、DE81イオン交換紙(Whatman, Hillsborough OR)上への電気泳動により2%低融点アガロースゲルから精製した。DNAフラグメントを、1M NaClを用いてこの紙から溶出してエタノール沈澱した。
精製されたフラグメントを、PCR Mix(0.2mM 各dNTP、2.2mM MgCl2、50mM KCl、10mM Tris−HCl pH 9.0、0.1% Triton X−100、0.3μl Taq DNAポリメラーゼ、50μlの総容量)中に10〜30ng/μlの濃度で再懸濁させた。この時点では、プライマーを添加しなかった。94℃60秒間、[94℃30秒間、50〜55℃30秒間、72℃30秒間]の30〜45サイクル、および72℃5分間の再組立プログラムを、MJ Research(Watertown MA)PTC−150サーマルサイクラーにおいて用いた。より大きな配列への小さなフラグメントのPCR再組立に続いて、再組立の25、30、35、40、および45サイクル後の反応のサンプルを採取した(図2)。
それぞれ0.8μMの上記のプライマー(配列番号1および2)を有するPCR Mixへの再組立産物の希釈、および約15サイクルのPCR(それぞれのサイクルは、[94℃30秒間、50℃30秒間、および72℃30秒間]からなる)の後、正確なサイズの単一の産物が得られた(図2)。
上記の工程4由来のPCR産物を、末端の制限酵素BamHIおよびEco0109で消化し、そして上記の工程2に記載のようにゲル精製した。再組立されたフラグメントを、BamHIおよびEco0109で消化したpUC18に連結した。E.coliを、製造業者(Stratagene, San Diego CA)により推奨されるような標準的な条件下で、この連結混合物を用いて形質転換し、そして100μg/mlアンピシリン、0.004% X−galおよび2mM IPTGを有するアガープレートに播いた。++組換え体と判定されるHinDIII−NheIフラグメントを有する得られたコロニーを、それが青く見えることにより同定した。
(1)LacZ遺伝子再編成)
2つのLacZ遺伝子構築物を用いて、75塩基離れた2つのマーカー間のクロスオーバーを計測した。終止コドンを、LacZα遺伝子の2つの離れた範囲に挿入し、ネガティブマーカーとして用いた。それぞれのマーカーは、4つの終止コドンを有する25bpの非相同配列であり、終止コドンのうち2つは、LacZ遺伝子のリーディングフレーム内にある。25bpの非相同配列を、大きな四角により図3に示す。終止コドンは、四角で囲むか、または下線を付すかした。+−および−+型のLacZα遺伝子(図3)を含有する2つの1.0kbのLacZテンプレートの1:1混合物を、DNAseIで消化し、そして100〜200bpのフラグメントを実施例1に記載のように精製した。再編成プログラムを、0.5μlのポリメラーゼを添加し、そして全容量が100μlであった以外は、実施例1における再組立について記載された条件と同様の条件下で実施した。
2.7kbプラスミド全体(pUC18−+およびpUC18+−)もまた、試験した。+−および−+型のLacZα遺伝子(図3)を含有する2つの2.9kbのプラスミドの1:1混合物を、DNAseIで消化し、そして100〜200bpのフラグメントを実施例1に記載のように精製した。プログラムが[94℃30秒間、55℃30秒間、72℃30秒間]の60サイクルであった以外は、上記の工程(1)における再組立について記載された条件と同様の条件下で再編成プログラムを実施した。ゲル分析は,再編成プログラム後、産物のほとんどが20kbよりも大きいことを示した。このようにして、2.7kbのプラスミド全体(pUC18−+およびpUC18+−)を、プライマーの添加なしにランダムな100〜200bpのフラグメントから効率的に再組立した。
再編成混合物中に混合されるオリゴヌクレオチドは、テンプレートDNAに対するオリゴヌクレオチドのフランキング配列の相同性に基づき最終産物中に取り込まれ得る(図4)。上述のLacZ-終止コドン変異体(pUC18−+)をDNAseI消化テンプレートとして用いた。両末端に野生型LacZ遺伝子に対する18塩基の相同性を含有する66マーのオリゴヌクレオチドを、4倍モル濃度過剰量で反応物中に添加し、本来の遺伝子中に存在する終止コドン変異を補正した。再編成反応を、上記の工程2における条件と同様の条件下で実施した。得られた産物を消化し、連結し、そして上述のようにE.coliに挿入した。
プラスミドpUC18を制限酵素EcoRI、Eco0109、XmnI、およびAlwNIで消化し、約370、460、770、および1080bpのフラグメントを産生した。これらのフラグメントを電気泳動し、そして2%低融点アガロースゲルから別々に精製した(370塩基対のバンドと460塩基対のバンドは、分離され得なかった)。これにより、3つの別個のチューブに、大きなフラグメント、中程度のフラグメント、および2つの小さなフラグメントの混合物を得た。
この実施例は、15塩基よりも少ない相同性に基づいてクロスオーバーが得られ得ることを説明する。例として、ヒトおよびマウスのIL−1β遺伝子を再編成した。
直接分子進化のための変異誘発DNA再編成の利用性を、βラクタマーゼモデルシステムにおいて試験した。TEM−1βラクタマーゼは、非常に効率的な酵素であり、主に拡散によりその反応速度は限定される。この実施例は、その反応特異性を変化すること、および通常加水分解しない薬物セフォタキシムに対して耐性を得ることが可能であるかを決定する。
細菌のTEM−1βラクタマーゼ遺伝子を保有するpUC18誘導体を用いた(28)。TEM−1βラクタマーゼ遺伝子は、細菌に約0.02μg/mlのセフォタキシムに対する耐性を与える。2つのプライマー:
プライマーA(配列番号7):
第1の再編成反応のための基質は、プライマーCおよびD(両方ともSfiI部位を含有する)を用いるpUC182SfiのPCRにより得られた0.9kbのdsDNAであった。
精製したフラグメントを、10〜30ng/μlの濃度でPCR混合物(0.2mM 各dNTP、2.2mM MgCl2、50mM KCl、10mM Tris−HCl pH 9.0、0.1% Triton X−100)に再懸濁した。この時点でプライマーを添加しなかった。94℃60秒間、次いで[94℃30秒間、50〜55℃30秒間、72℃30秒間]の40サイクル、そして次いで72℃5分間の再組立プログラムを、MJ Research(Watertown MA)PTC−150サーマルサイクラーにおいて使用した。
0.8μMのそれぞれのプライマー(CおよびD)を有するPCR混合物への再組立産物の希釈、および20のPCRサイクル[94℃30秒間、50℃30秒間、72℃30秒間]の後、900bpのサイズの単一の産物を得た。
末端の制限酵素SfiIでの900bp産物の消化、およびアガロースゲル精製の後、900bp産物を、T4 DNAリガーゼ(BRL, Gaithersburg MD)を用いて唯一のSfiI部位でベクターpUC182Sfiに連結した。混合物を、E.coli XL1−blue細胞にエレクトロポレートし、そして0.32〜0.64μg/mlのセフォタキシム(Sigma,
St.Louis MO)を有するLBプレートに播いた。細胞を、37℃で24時間まで増殖させ、得られたコロニーをプールとしてプレートから掻き取り、そして次のラウンドの再編成のためのPCRテンプレートとして用いた。
3ラウンドの再編成のそれぞれの後に得られた形質転換体を、漸増するレベルのセフォタキシムに播いた。最も高いレベルのセフォタキシムを有するプレート由来のコロニー(>100、多様性を維持するために)をプールし、次のラウンドのPCR反応のためのテンプレートとして用いた。
1,280μg/mlで生育した5つの最も大きいコロニーの全ては、野生型TEM−1酵素と同一な制限地図を有した。これらのコロニーの内の1つから得られたプラスミドのSfiI挿入物を、製造業者の指示に従い、ジデオキシDNA配列決定法(United States Biochemical Co., Cleveland OH)により配列決定した。全ての塩基番号は、改訂されたpBR322配列(29)に対応し、そしてアミノ酸番号は、ABL標準番号付けスキーム(30)に対応する。アミノ酸は3文字表記で示され、そしてヌクレオチドは1文字表記で示される。用語G4205Aは、ヌクレトチド4205が、グアニジンからアデニンに変化したことを意味する。
次いで非必須変異を除去するために、過剰量の野生型DNAを用いた分子戻し交雑を用いた。
野生型プラスミド、非戻し交雑変異体、および戻し交雑変異体におけるβラクタマーゼ遺伝子の発現レベルを、Witholt, B.(32)の方法に従い浸透圧ショックにより調製された周辺質の抽出物のSDS−ポリアクリルアミドゲル電気泳動(4〜20%;Novex, San Diego CA)により比較した。
変異の異なる組み合わせの耐性を決定するため、そして発表された変異体と新規の変異体とを比較するために、いくつかの変異体を、同一のプラスミドバックグラウンド中に構築した。2つの変異(Glu104LysおよびGly238Ser)は、セフォタキシム変異体として知られている。構築した全ての変異体の組み合わせは、プロモーター変異を有しており、これは選択された変異体の比較を可能にした。結果を図4に示す。
A10B scFv抗体、マウス抗ウサギIgGは、Pharmacia(Milwaukee WI)から寄贈された。pCANTAB5ファージディスプレイベクターを使用する市販のPharmaciaファージディスプレイシステムを使用した。
OH)。Kabat(33)との比較に基づくと、この配列は、既存の抗体と同様であった。
A10B野生型抗体遺伝子を有するファージDNA(10μl)を、99℃にて10分間インキュベートし、次いで72℃にて2分間インキュベートした。PCR混合物(50mM KCl、10mM Tris−HCl pH 9.0、0.1% Triton X−100、200μM 各dNTP、1.9mM MgCl)、0.6μmのそれぞれのプライマー、および0.5μl Taq DNAポリメラーゼ(Promega, Madison WI)をファージDNAに添加した。PCRプログラムを[94℃30秒間、45℃30秒間、72℃45秒間]の35サイクルにわたって実施した。用いたプライマーは:
5' ATGATTACGCCAAGCTTT 3'(配列番号26)および
5' TTGTCGTCTTTCCAGACGTT 3'(配列番号27)
であった。
300ngのゲル精製した850bpのバンドを、20分間室温にて、50mM Tris−HCl pH 7.5、10mM MgCl中で0.18単位のDNAse I(Sigma, St.Louis MO)で消化した。消化したDNAを、2%低融点アガロースゲルにおいて分離し、そして50〜200bp間のバンドをゲルから精製した。
本実験の目的は、CDRの挿入が効果的であるか否かを試験することである。
KCl、10mM Tris−HCl pH9.0、0.1% Triton
X−100、1.9mM MgCl、200μmの各dNTP、0.3μl Taq DNAポリメラーゼ(Promega、Madison WI)、総容積50μl)を添加し、そして94℃で1分間、72℃で1分間、次いで35サイクル:94℃で30秒間、55℃で30秒間、72℃で30秒間の再編成プログラムを行った。
外側プライマー1:配列番号27
5’ TTGTCGTCTTTCCAGACGTT 3’
外側プライマー2:配列番号26
5’ ATGATTACGCCAAGCTTT 3’
850bpのPCR生成物を制限酵素SfiIおよびNotIで消化し、低融点アガロースゲルから精製し、そしてPharmacia、Milwaukee
WIから得たpCANTAB5発現ベクターに連結した。Invitrogen (San Diego CA)により記載される方法に従って、 連結したベクターをTG1細胞(Pharmacia、Milwaukee WI)にエレクトロポレートし、そして単一のコロニーについてプレートした。
本発明者らの配列データに基づき、6つのCDRに対応する6オリゴヌクレオチドを作製した。CDR(Kabat定義)を70(個の存在塩基):10:10:10の比率で合成的に変異を誘発し、そして約20塩基のフランキング配列により5’末端および3’末端側に側面を接しさせた。このフランキング配列は、変異を誘発しない抗体遺伝子フラグメントの混合物に過剰なモル量で混合する場合、CDRの取り込みに対して相同性を提供する。得られる変異配列を以下に示す。
850bpのPCR生成物を制限酵素SfiIおよびNotIで消化し、低融点アガロースゲルから精製し、そしてPharmacia、Milwaukee
WIから得たpCANTAB5発現ベクターに連結した。Invitrogen (San Diego CA)により記載される方法に従って連結したベクターをTG1細胞(Pharmacia Milwaukee WI)にエレクトロポレートし、そして製造業者により推薦されるガイドラインに従ってヘルパーファージを用いてファージライブラリーを増殖させた。
96ウェルのマイクロタイタープレートの15ウェルを、ウサギIgG(Jackson Immunoresearch、Bar Harbor ME)で10μg/ウェル、37℃で1時間コートし、次いでPBS中の2%のノンファットドライミルクで37℃で1時間ブロックした。
プラスミドを2つの部分で構築した。この2つの部分は、これらの2つのダイレクトリピートの共通範囲間の組換えが完全長の活性組換え遺伝子をもたらすことを示す同一遺伝子(β−ラクタマーゼ)の不活性コピーである。
2つのプライマーの配列:
β−ラクタマーゼ遺伝子の異なる対立遺伝子の2つの完全長コピーを有するプラスミドを構築した。2つの遺伝子の相同組換えによりこの遺伝子の1つの組換え完全長コピーを得た。
このプラスミドをE.coli細胞内にエレクトロポレートした。この細胞を15μg/mlのテトラサイクリンを含有する固体寒天プレート上にプレートした。次いで増殖したこれらのコロニーを100μg/mlのアンピシリンを含有する固体寒天プレート上にプレートし、そして生存するコロニーの数をカウントした。アンピシンリン耐性を示すこれらの形質転換体中のBla挿入物を、実施例8に記載される方法およびプライマーを使用する標準的なPCR技術により増幅した。1kbの挿入物の存在は、表6に示されるように重複遺伝子(duplicate gene)が組換えられたことを示す。
さらに迅速に耐性細胞を生産するために多数サイクルの組換えを用い得るか否かを決定するために、実施例9に記載される多数サイクルの方法を行った。
pUC18Sfi−Bla−Sfiを含む適切なE.coli細胞を記載のように調製した。プラスミドpUC18Sfi−Bla−Sfiは、前出に記載のような標準的なTEM−1 β−ラクタマーゼ遺伝子を含有する。
最適化された表現型(例えば、クローン化遺伝子のようなベクターがコードされる配列の最大の発現)を与え得るベクターを提供するために、再編成され得る種々のカセットを含むキットが提供され、そして最適化された再編成体が選択され得る。図12は、それぞれの遺伝子座が複数のカセットを有する1つの実施態様を概略的に示す。例えば、細菌の発現システムにおいて、図13はそれぞれの遺伝子座で使用される例示のカセットを示す。与えられた遺伝子座のそれぞれのカセット(例えば、本実施例のすべてのプロモーター)は、隣接する遺伝子座のカセットのフランキング配列に重複し得、そしてまた、好ましくは相同組換えまたは非相同性組換えに関与し得る(例えば、lox/creまたはflp/frt系)実質的に同一な配列と隣接し、遺伝子座内であるが実質的に遺伝子座間ではないカセットの再編成を提供するようにする。
以下の文献は、本出願の関連する部分で本出願において引用される。
Claims (6)
- 所定の抗原に特異的に結合する抗体鎖をコードするポリヌクレオチドを生成する方法であって、該方法は、以下の複数のサイクル:
(a)重鎖CDR領域および/または軽鎖CDR領域をコードする基質ポリヌクレオチドの集団のセグメントを変性する工程であって、ここで、該重鎖CDR領域および/または軽鎖CDR領域をコードする基質ポリヌクレオチドの集団のセグメントは、それぞれ、各重鎖CDRおよび/または軽鎖CDRの異なる形態をコードする複数のオリゴヌクレオチドを含む、工程;
(b)該変性されたセグメントをアニーリングする工程;
(c)該アニーリングされたセグメントを、ポリメラーゼの存在下でインキュベートし、それにより該基質ポリヌクレオチドによりコードされるものとは異なる重鎖CDRおよび/または軽鎖CDRの組合せを有する抗体鎖をコードする組換えポリヌクレオチドの集団を形成する工程;ならびに
(d)該ポリヌクレオチドの集団をスクリーニングまたは選択して、該所定の抗原に特異的に結合する抗体鎖をコードする少なくとも1つのポリヌクレオチドを同定する工程、
を実施する工程を包含する、方法。 - 前記ポリヌクレオチドの集団の少なくとも10%が、CDR領域の新規の組合せを有する組換えポリヌクレオチドを構成する、請求項1に記載の方法。
- バクテリオファージディスプレイシステムを使用してスクリーニングまたは選択する工程を包含する、請求項1に記載の方法。
- 宿主細胞における所定の抗原に特異的に結合する抗体鎖をコードする少なくとも1つの組換えポリヌクレオチドを発現する工程をさらに包含する、請求項1に記載の方法。
- 前記抗体が、少なくとも約109M−1の親和性で特異的に結合する、請求項4に記載の方法。
- 前記抗体が、少なくとも約1010M−1の親和性で特異的に結合する、請求項4に記載の方法。
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