TWI814094B - 貓抗體變異體 - Google Patents
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Abstract
本發明大體上係關於貓抗體變異體及其用途。特定言之,本發明係關於貓抗體恆定區中用於改良其半衰期及其他特徵之突變。
Description
本發明大體上係關於貓抗體變異體及其用途。特定言之,本發明係關於貓抗體之Fc恆定區中用於改良半衰期及其他特徵的突變。
貓IgG單株抗體(mAb)將研發作為獸醫學中之有效治療劑。幾年前,鑑別且表徵四種貓IgG子類(Strietzel等人,2014,
Vet Immunol Immunopathol. 第158(3-4)卷,第214至223頁)。然而,並未對延長貓IgG之半衰期的進行足夠研究。
經由再循環機制,新生兒Fc受體(FcRn)以與其片段可結晶(Fc)區之pH依賴性相互作用延長IgG之半衰期。特定言之,跨越CH2及CH3域之界面的Fc區與細胞表面上之FcRn相互作用以調節IgG內環境穩定。IgG胞飲作用之後的酸性相互作用有助於此相互作用且因此避免IgG降解。內吞IgG接著再循環回至細胞表面且以鹼性pH經釋放進入血流中,藉此保持足夠的血清IgG以發揮恰當功能。因此,IgG之藥物動力學概況視其Fc區之結構及功能特性而定。
三種貓IgG子類結合貓FcRn且已經與人類IgG類似物進行比較。貓IgG之半衰期仍需要進行充分研究,因為在無任何實驗支援的情況下,吾人不能預期或預測其是否將與人類IgG緊密對準。
延長IgG之半衰期可允許抗體藥物之不太頻繁給藥及/或較低劑量,其繼而減少獸醫問診,提高患者順應性,且降低濃度依賴性細胞毒性/不良事件。
因此,需要鑑別Fc恆定區中用以提高半衰期之突變。
本發明係關於突變貓IgG,相對於野生型貓IgG,該突變貓IgG提供更高的FcRn親和力及更高的半衰期。特定言之,本申請案之本發明人發現,位置428或434之胺基酸殘基絲胺酸(Ser或S)經另一胺基酸取代出人意料地且未預期地增強了針對FcRn之親和力,且藉此延長了IgG之半衰期。
在一個態樣中,本發明提供一種經修飾之IgG,其包含:相對於野生型貓IgG恆定域,包含至少一個胺基酸取代之貓IgG恆定域,其中該取代處於根據如Kabat中之EU索引編號的胺基酸殘基428或434。在一例示性實施例中,該取代為位置428之絲胺酸經白胺酸取代(S428L)。在另一例示性實施例中,該取代為位置434之絲胺酸經組胺酸取代(S434H)。在一些實施例中,貓IgG恆定域包含428及434位置之絲胺酸分別經白胺酸及組胺酸取代。
在另一態樣中,本發明提供一種多肽,其包含:相對於野生型貓IgG恆定域,包含一或多種胺基酸取代之貓IgG恆定域,其中該一或多種取代處於胺基酸殘基428、434或其組合。
在又一態樣中,本發明提供一種抗體或分子,其包含:相對於野生型貓IgG恆定域,包含一或多種胺基酸取代之貓IgG恆定域,其中該一或多種取代處於胺基酸殘基428、434或其組合。
在另一態樣中,本發明提供一種用於產生或製造抗體或分子之方法,該方法包含:提供具有包含貓IgG恆定域之抗體的載體或宿主細胞,相對於野生型貓IgG恆定域,該貓IgG恆定域包含一或多種胺基酸取代,其中該一或多種取代處於胺基酸殘基428、434或其組合。
在另一態樣中,本發明提供一種用於延長貓之抗體血清半衰期之方法,該方法包含:向該貓投與治療有效量之包含貓IgG恆定域之抗體,相對於野生型貓IgG恆定域,該貓IgG恆定域包含一或多種胺基酸取代,其中該一或多種取代處於胺基酸殘基428、434或其組合。
本發明之其他特徵及優勢將自以下詳細描述實例及圖式變得顯而易知。然而,應理解,詳細描述及特定實例雖然指示本發明之較佳實施例,但僅以說明方式給出,因為熟習此項技術者將由此詳細描述而對本發明之精神及範疇內的各種改變及修正變得顯而易知。
相關申請案之交叉參考
本申請案主張2020年9月29日申請的美國臨時專利申請案第63/084,693號的優先權及權益,該美國臨時專利申請案特此以全文引用的方式併入本文中。
參考形成本發明之一部分的以下詳細描述,可更容易地理解本發明之主題。應理解,本發明不限於本文所描述及/或展示之具體產物、方法、條件或參數,且本文所用之術語僅借助於實例出於描述特定實施例的目的,且不意欲限制任何所主張之本發明。
除非本文中另外定義,否則結合本申請使用之科學及技術術語應具有一般技術者通常所理解之含義。此外,除非上下文另外需要,否則單數術語應包括複數形式且複數術語應包括單數形式。
如在本發明中使用,除非另外指明,否則以下術語及縮寫應理解具有以下含義。
定義
在本發明中,除非上下文另外明確指示,否則單數形式「一(a/an)」及「該(the)」包括複數個參考物,且特定數值之引用包括至少該特定值。因此,舉例而言,提及「分子(a molecule)」或「化合物(a compound)」係提及一或多種此類分子或化合物及熟習此項技術者已知之其等效物等。如本文所用,術語「複數個(種)」意謂多於一個(種)。當表示值範圍時,另一實施例包括自一個特定值及/或至另一個特定值。類似地,當藉由在前面使用「約」以近似值表示值時,應理解,該特定值形成另一實施例。所有範圍均為包括性及可組合的。
在說明書及申請專利範圍中,免疫球蛋白重鏈中之胺基酸殘基之編號係如Kabat等人, Sequences of Proteins of Immunological Interest, 第5版. Public Health Service, National Institutes of Health, Bethesda, Md. (1991)中之Eu索引的編號。「如Kabat中之Eu索引」係指IgG抗體之殘基編號且反映於本文中之圖2A中。
術語「經分離」在結合核酸使用時為自其天然來源中通常與其相關之至少一種污染物核酸中鑑別且分離出之核酸。經分離之核酸可以與自然界中發現的形式或環境不同的形式或環境存在。因此,經分離之核酸分子區別於在天然細胞中存在的核酸分子。經分離之核酸分子包括細胞中含有之通常表現本文中所編碼之多肽的核酸分子,其中例如該核酸分子處於與天然細胞之質粒或染色體位置不同的質粒或染色體位置。經分離之核酸可以單股或雙股形式存在。當利用經分離之核酸分子表現蛋白質時,寡核苷酸或聚核苷酸將含有最小有義股或編碼股,但可含有有義股及反義股兩者(亦即,可為雙股)。
當核酸分子與另一核酸分子處於功能關係時,該核酸分子經「可操作地連接(operably linked/operably attached)」。舉例而言,若啟動子或強化子影響序列之轉錄,則該啟動子或強化子係可操作地連接至核酸之編碼序列;或若核糖體結合位點經定位以促進轉譯,則核糖體結合位點係可操作地連接至核酸之編碼序列。若編碼變異Fc區之核酸分子經定位而使得經表現之融合蛋白包含與變異Fc區多肽上游或下游鄰接之異源蛋白質或其功能片段,則其可操作地連接於編碼異源蛋白質(亦即,當其存在於自然界中時不包含Fc區的蛋白質或其功能片段)之核酸分子;異源蛋白質可緊鄰變異Fc區多肽或可藉由任何長度及組成之連接子序列與其間隔開。同樣地,當多肽(在本文中與「蛋白質」同義地使用)分子與另一多肽處於功能關係時,該多肽分子經「可操作地連接」。
如本文中所使用,術語「功能片段」參考多肽或蛋白質(例如,變異Fc區或單株抗體)時,係指保留全長多肽之至少一個功能的彼蛋白質片段。片段之大小可介於六個胺基酸至全長多肽之全部胺基酸序列減一個胺基酸的範圍內。本發明之變異Fc區多肽之功能片段保留至少一種如本文所定義之「胺基酸取代」。變異Fc區多肽之功能片段保留此項技術中已知的與Fc區相關之至少一個功能(例如,ADCC、CDC、Fc受體結合、Clq結合、細胞表面受體之下調或可例如增加與其可操作連接之多肽之活體內或活體外半衰期)。
術語「經純化」或「純化」係指自樣品實質性移除至少一種污染物。舉例而言,抗原特異性抗體可藉由完全或實質性移除(至少90%、91%、92%、93%、94%、95%,或更佳地至少96%、97%、98%或99%)至少一種污染性非免疫球蛋白蛋白質來純化;其亦可藉由移除並未結合於相同抗原之免疫球蛋白蛋白質來純化。移除非免疫球蛋白蛋白質及/或移除並未結合特定抗原之免疫球蛋白使得樣品中抗原特異性免疫球蛋白之百分比增加。在另一實施例中,細菌性宿主細胞中表現之多肽(例如,免疫球蛋白)藉由完全或實質性移除宿主細胞蛋白質來純化;藉此增加樣品中多肽之百分比。
術語「天然的」在指代多肽(例如,Fc區)時在本文中用以指示該多肽具有由自然界中通常存在之多肽或其天然存在之多晶型之胺基酸序列組成的胺基酸序列。天然多肽(例如,天然Fc區)可藉由重組方式製備或可自天然存在源分離。
如本文所使用,術語「表現載體」係指含有所需編碼序列及在特定宿主生物體中表現可操作地連接之編碼序列所需之適當核酸序列的重組DNA分子。
如本文中所使用,術語「宿主細胞」係指位於活體外或原位或活體內的任何真核或原核細胞(例如,細菌細胞,諸如大腸桿菌;CHO細胞、酵母菌細胞、哺乳動物細胞、禽類細胞、兩棲動物細胞、植物細胞、魚細胞及昆蟲細胞)。
如本文中所使用,術語「Fc區」係指免疫球蛋白重鏈之C端區。「Fc區」可為天然序列Fc區或變異Fc區。儘管免疫球蛋白重鏈之Fc區之一般可接受的邊界可不同,但貓IgG重鏈Fc區通常被限定以例如自位置231之胺基酸殘基延伸至其羧基端。在一些實施例中,變異體僅包含Fc區之部分且可包括或不包括羧基端。免疫球蛋白之Fc區一般包含兩個恆定域:CH2及CH3。在一些實施例中,涵蓋具有一或多個恆定域之變異體。在其他實施例中,涵蓋不含此類恆定域(或僅含此類恆定域之部分)之變異體。
貓IgG Fc區之「CH2域」通常自例如約胺基酸231延伸至約胺基酸340 (參見圖2A)。CH2域的獨特之處在於其不與另一域緊密配對。兩個N連接之分支鏈碳水化合物鏈插入於完整天然IgG分子之兩個CH2域之間。
貓IgG Fc區之「CH3域」通常為Fc區延伸中之CH2域之C端殘基延伸段,例如自約胺基酸殘基341至約胺基酸殘基447 (參見圖2A)。
「功能性Fc區」具有天然序列Fc區之「效應功能」。相對於包含天然Fc區或變異體之親本Fc區的多肽,包含本發明之變異Fc區的多肽之至少一種效應功能可增強或減弱。效應功能之實例包括(但不限於):Clq結合;補體依賴性細胞毒性(CDC);Fc受體結合;抗體依賴性細胞介導之細胞毒性(ADCC);吞噬作用;細胞表面受體(例如,B細胞受體;BCR)之下調等。此類效應功能可能需要可操作地連接於結合域(例如抗體可變域)之Fc區且可使用各種分析(例如,Fc結合分析、ADCC分析、CDC分析、全血樣品或分級分離之血液樣品的目標細胞消耗等)來評估。
「天然序列Fc區」或「野生型Fc區」係指與在自然界中通常發現之Fc區之胺基酸序列具有一致性之胺基酸序列。例示性天然序列貓Fc區展示於圖2A中且包括例如貓IgG1a Fc區之天然序列。
「變異Fc區」包含與天然序列Fc區(或其片段)之胺基酸序列相差至少一個如本文所定義之「胺基酸取代」的胺基酸序列。在較佳實施例中,變異Fc區相比於天然序列Fc區或在親本多肽之Fc區中具有至少一個胺基酸取代,較佳地在天然序列Fc區中或在親本多肽之Fc區中具有1、2、3、4或5個胺基酸取代。在一替代實施例中,變異Fc區可根據本文中所揭示之方法產生且此變異Fc區可與所選異源多肽(諸如抗體可變域或非抗體多肽(例如,受體或配位體之結合域))融合。
如本文中所使用,在多肽之上下文中的術語「衍生物」係指包含已藉由引入胺基酸殘基取代而變異之胺基酸序列的多肽。如本文中所使用,術語「衍生物」亦指已藉由任何類型之分子與多肽之共價附接經修飾的多肽。舉例而言(但不以限制方式),抗體可例如藉由糖基化、乙醯化、聚乙二醇化、磷酸化、醯胺化、由已知保護/阻斷基團進行之衍生化、蛋白水解裂解、與細胞配位體或其他蛋白連接等來修飾。A 衍生物多肽可藉由使用熟習此項技術者已知之技術進行化學修飾來製備,該等技術包括(但不限於)特定化學裂解、乙醯化、甲醯化、衣黴素之代謝合成等。此外,衍生物多肽具有與衍生其之多肽類似或相同的功能。應瞭解包含本發明之變異Fc區的多肽可為如本文所定義之衍生物,較佳地,衍生化發生在Fc區內。
如本文中所使用,關於多肽(例如,Fc區或單株抗體)之「實質上之貓來源」指示該多肽具有與天然貓胺基多肽之胺基酸序列至少80%、至少85%、更佳地至少90%、91%、92%、93%、94%或甚至更佳地至少95%、95%、97%、98%或99%同源性的胺基酸序列。
術語「Fc受體」或「FcR」用於描述結合至Fc區 (例如,抗體之Fc區)的受體。較佳FcR係天然序列FcR。此外,較佳FcR為結合IgG抗體(γ受體)且包括FcγRI、FcγRII及FcγRIII子類之受體(包括此等受體之對偶基因變異體及交替剪接形式)的FcR。另一較佳FcR包括新生受體FcRn,其負責將母體IgG轉移至胎兒(Guyer等人,J. Immunol. 117:587 (1976)及Kim等人,J . Immunol .24:249 (1994))。本文中之術語「FcR」涵蓋其他FcR,包括將來鑑別之FcR。
片語「抗體依賴性細胞介導之細胞毒性」及「ADCC」係指細胞介導之反應,其中表現FcR之非特異性細胞毒性細胞(例如,非特異性) (例如,自然殺手(「NK」)細胞、嗜中性球及巨噬細胞)識別目標細胞上之經結合抗體且隨後使得目標細胞裂解。用於介導ADCC之原代細胞NK細胞僅表現FcγRIII,而單核球表現FcγRI、FcγRII及FcγRIII。
如本文中所使用,片語「效應細胞」係指表現一或多種FcR且執行效應功能之白血球(較佳地貓)。較佳地,該等細胞至少表現FcγRIII且執行ADCC效應功能。介導ADCC之白血球之實例包括PBMC、NK細胞、單核球、細胞毒性T細胞及嗜中性球。效應細胞可自天然來源(例如自血液或PBMC)分離。
具有「變化」FcRn結合親和力之變異多肽為在pH 6.0下量測時,與變異體之親本多肽或包含天然Fc區之多肽相比,具有增強(亦即,增加的、更大的或更高的)或減弱(亦即降低的、更小的或更低的) FcRn結合親和力之多肽。顯示與FcRn之結合增加或結合親和力增加的變異多肽以相比於親本多肽更大的親和力結合FcRn。A 顯示與FcRn之結合減小或結合親和力減小的變異多肽以相比於其親本多肽更低的親和力結合FcRn。顯示與FcRn之結合減小的此類變異體可具有與FcRn很少或沒有可觀的結合,例如與親本多肽相比,0%至20%與FcRn之結合。與其親本多肽相比,以「增強親和力」結合FcRn之變異多肽為當結合分析中變異多肽及親本多肽之量基本上相同,且所有其他條件一致時,以比親本多肽更高之結合親和力結合FcRn的多肽。舉例而言,具有增強FcRn結合親和力之變異多肽可顯示相比於親本多肽,FcRn結合親和力增加約1.10倍至約100倍(更通常約1.2倍至約50倍),其中例如在ELISA分析或一般熟習此項技術者可用之其他方法中測定FcRn結合親和力。
如本文中所使用,「胺基酸取代」係指給定胺基酸序列中之至少一個現有胺基酸殘基經另一不同「置換」胺基酸殘基置換。該或該等置換殘基可為「天然存在之胺基酸殘基」(亦即,由遺傳密碼編碼)且選自由以下組成之群:丙胺酸(Ala);精胺酸(Arg);天冬醯胺(Asn);天冬胺酸(Asp);半胱胺酸(Cys);麩醯胺酸(Gln);麩胺酸(Glu);甘胺酸(Gly);組胺酸(His);異白胺酸(Ile):白胺酸(Leu);離胺酸(Lys);甲硫胺酸(Met);苯丙胺酸(Phe);脯胺酸(Pro);絲胺酸(Ser);蘇胺酸(Thr);色胺酸(Trp);酪胺酸(Tyr);及纈胺酸(Val)。本文中之胺基酸取代定義亦涵蓋一或多個非天然存在之胺基酸殘基取代。「非天然存在之胺基酸殘基」係指除上文所列之彼等天然存在之胺基酸殘基以外的能夠共價結合多肽鏈中之一或多個相鄰胺基酸殘基的殘基。非天然存在之胺基酸殘基之實例為正白胺酸、鳥胺酸、正纈胺酸、高絲胺酸及其他胺基酸殘基類似物,諸如Ellman等人,Meth. Enzym. 202:301-336 (1991)中所述者。
術語「分析信號」係指偵測蛋白質-蛋白質相互作用之任何方法的輸出,包括(但不限於)比色分析之吸光度量測、螢光強度或衰變數/分鐘。分析格式可包括ELISA、facs或其他方法。「分析信號」之變化可反映細胞存活率之變化及/或動力學解離速率、動力學締合速率或兩者之變化。「更高分析信號」係指所量測的大於另一數值之輸出數值(例如,在ELISA分析中,與親本多肽相比,變異體可以具有更高(更大)的量測數值)。A 「更低」分析信號係指所量測的小於另一數值之輸出數值(例如,在ELISA分析中,與親本多肽相比,變異體可以具有更低的(較小)量測數值)。
術語「結合親和力」係指與各Fc受體-Fc結合相互作用相關之平衡解離常數(以濃度單位表述)。結合親和力直接與動力學解離速率(通常以倒數時間單位報導,例如秒
-1)除以動力學締合速率(通常以每單位時間之濃度單位報導,例如莫耳/秒)之比率相關。一般而言,不可能明確地表明平衡解離常數之變化是否是由於締合速率、解離速率或兩者之差異而導致,除非此等參數中之每一者以實驗方式經測定(例如,藉由BIACORE或SAPIDYNE量測)。
如本文中所使用,術語「鉸鏈區」係指例如貓IgG1a中之胺基酸延伸(例如,貓IgG1a之位置216延伸至位置230)。其他IgG同型之鉸鏈區可藉由將形成重鏈間二硫(S-S)鍵之第一個及最後一個半胱胺酸殘基置放在相同位置而與IgG序列對齊。
「Clq」為包括針對免疫球蛋白之Fc區之結合位點的多肽。Clq連同兩種絲胺酸蛋白酶Clr及Cls形成複合體Cl (CDC路徑之第一組分)。
如本文中所使用,術語「抗體」可與「免疫球蛋白」互換使用或「Ig」以最廣泛的意義使用且特定地涵蓋單株抗體(包括全長單株抗體)、多株抗體、多特異性抗體(例如雙特異性抗體)及抗體片段,隻要其展現所需生物活性或功能活性。本發明及術語「抗體」亦涵蓋包含來源於不同物種之部分的單鏈抗體及嵌合、貓或貓類化抗體,以及嵌合或CDR移植之單鏈抗體等。此等抗體之各種部分可藉由習知技術化學地、合成地連接在一起或可使用基因工程改造技術製備為連續蛋白。舉例而言,編碼嵌合或貓類化鏈之核酸可表現以產生連續蛋白質。參見例如,美國專利第4,816,567號;美國專利第4,816,397號;WO 86/01533;美國專利第5,225,539號;及美國專利第5,585,089號及第5,698,762號。關於靈長類化抗體亦參見Newman,R.等人,BioTechnology, 10:1455-1460, 1993,且關於單鏈抗體,參見Ladner等人,美國專利第4,946,778號及Bird,R.E.等人,Science, 242:423-426, 1988。應瞭解,包含Fc區(或其部分)之抗體之所有形式涵蓋於本文中之術語「抗體」中。此外,抗體可用可偵測標記來標記,固定於固相上及/或根據此項技術中已知之方法與異源化合物(例如,酶或毒素)共軛。
如本文中所使用,術語「抗體片段」係指完整抗體之一部分。抗體片段之實例包括(但不限於)直鏈抗體;單鏈抗體分子;Fc或Fc之肽、Fab及Fab片段,及由抗體片段形成之多特異性抗體。抗體片段較佳地保留鉸鏈之至少一部分且視情況IgG重鏈之CH1區。在其他較佳實施例中,抗體片段包含CH2區之至少一部分或整個CH2區。
如本文中所使用,當術語「功能片段」關於單株抗體使用時意欲指代單株抗體仍保留功能活性之部分。功能活性可為例如抗原結合活性或特異性、受體結合活性或特異性、效應功能活性等。單株抗體功能片段包括例如單獨的重鏈或輕鏈及其片段,諸如VL、VH及Fd;單價片段,諸如Fv、Fab及Fab';二價片段,諸如F(ab')2;單鏈Fv(scFv);及Fc片段。此類術語描述於例如Harlowe及Lane,Antibodies:A Laboratory Manual, Cold Spring Harbor Laboratory, New York (1989);Molec. Biology and Biotechnology:A Comprehensive Desk Reference (Myers, R. A. (編), New York:VCH Publisher, Inc.);Huston等人, Cell Biophysics, 22:189-224 (1993);Pluckthun及Skerra, Meth. Enzymol., 178:497-515 (1989)及Day, E. D., Advanced Immunochemistry, 第二版, Wiley-Liss, Inc., New York, N.Y. (1990)中。術語功能片段意欲包括例如藉由蛋白酶消化或人類單株抗體之還原及藉由熟習此項技術者已知之重組DNA方法產生之片段。
如本文中所使用,術語「片段」係指包含另一多肽之胺基酸序列之至少5、15、20、25、40、50、70、90、100或更多個相鄰胺基酸殘基之胺基酸序列的多肽。在一較佳實施例中,多肽之片段保留全長多肽之至少一個功能。
如本文中所使用,術語「嵌合抗體」包括單價、二價或多價免疫球蛋白。單價嵌合抗體為由嵌合重鏈經由與嵌合輕鏈之二硫橋鍵締合形成的二聚體。二價嵌合抗體為由兩個重鏈-輕鏈二聚體經由至少一個二硫橋鍵締合形成的四聚體。用於貓之抗體之嵌合重鏈包含來源於非貓抗體之重鏈的與貓重鏈恆定區之至少一部分,諸如CH1或CH2連接的抗原結合區。用於貓之抗體之嵌合輕鏈包含來源於非貓抗體之輕鏈的與貓輕鏈恆定區(CL)之至少一部分連接的抗原結合區。具有相同或不同可變區結合特異性之嵌合重鏈及輕鏈的抗體、片段或衍生物亦可藉由個別多肽鏈根據已知方法步驟之適當締合來製備。藉由此途徑,將表現嵌合重鏈之宿主與表現嵌合輕鏈之宿主單獨培養,且免疫球蛋白鏈經單獨地回收且接著進行締合。替代地,宿主可進行共培養且使各鏈在培養基中自發地締合,接著回收經組裝之免疫球蛋白或片段,或重鏈及輕鏈均可在相同宿主細胞中表現。用於產生嵌合抗體之方法為此項技術中熟知的(參見例如美國專利第6,284,471號;第5,807,715號;第4,816,567號;及第4,816,397號)。
如本文中所使用,非貓(例如鼠類)抗體之「貓類化」形式(亦即,貓類化抗體)為含有來源於非貓免疫球蛋白之最少序列或沒有來源於非貓免疫球蛋白之序列的抗體。在極大程度上,貓類化抗體係貓免疫球蛋白(接受者抗體),其中來自接受者的高變區之殘基經來自諸如具有所需特異性、親和力及能力之小鼠、大鼠、兔、人類或非人類靈長類動物之非貓物種(供者抗體)的高變區之殘基置換。在一些情況下,貓免疫球蛋白之構架區(FR)殘基經相應的非貓殘基置換。此外,貓類化抗體可包含在接受者抗體或供者抗體中未發現之殘基。通常進行此等修飾以進一步改進抗體效能。一般而言,貓類化抗體將包含基本上全部至少一個,且通常兩個可變域,其中全部或基本上全部高變環(CDR)對應於非貓免疫球蛋白之彼等高變環且全部或基本上全部FR殘基為貓免疫球蛋白序列之彼等FR殘基。貓類化抗體亦可包含免疫球蛋白恆定區之至少一部分(Fc),通常貓免疫球蛋白之至少一部分。
如本文中所使用,術語「免疫黏附素」表示將異源「黏附素」蛋白質(例如,受體、配位體或酶)之結合域與免疫球蛋白恆定域組合之抗體樣分子。在結構上,免疫黏附素包含除抗體(亦即,為「異源」)之抗原識別及結合位點(抗原組合位點)以外的黏附素胺基酸序列以所需結合特異性與免疫球蛋白恆定域序列之融合。
如本文中所使用,術語「配位體結合域」係指任何天然受體或保持對應天然受體之至少一種定性配位體結合能力的其任何區或衍生物。在某些實施例中,受體來自具有與免疫球蛋白超基因家族成員同源之胞外域的細胞表面多肽。不為免疫球蛋白超基因家族成員,但此定義仍然特定涵蓋之其他受體為細胞因子之受體,且特定言之具有酪胺酸激酶活性之受體(受體酪胺酸激酶) (造血素及神經生長因子受體超家族之成員),及細胞黏附分子(例如,E-選擇素、L-選擇素及P-選擇素)。
如本文中所使用,術語「受體結合域」係指受體之任何天然配位體,包括例如細胞黏附分子,或此類天然配位體之保持對應天然配位體之至少一種定性受體結合能力的任何區或衍生物。
如本文中所使用,「經分離」多肽為自其天然環境之組分鑑別及分離及/或回收之多肽。其天然環境之污染組分為將干擾多肽之診斷或治療用途之物質,且可包括酶、激素及其他蛋白質或非蛋白質溶質。在某些實施例中,經分離多肽經純化(1)至大於95重量%之多肽,如藉由洛瑞法(Lowry method)所測定,且更佳大於99重量%,(2)在一定程度上藉由使用旋轉杯式定序儀(spinning cup sequenator)足以獲得至少15個N端殘基或內部胺基酸序列,或(3)藉由SDS-page在還原或非還原條件下使用庫馬斯藍或銀染色(Coomassie blue or silver stain)達至均質性。經分離之多肽包括原位存在於重組細胞內之多肽,因為多肽之天然環境中的至少一種組分將不存在。然而,通常經分離之多肽將藉由至少一個純化步驟來製備。
如本文中所使用,術語「病症」及「疾病」可互換地使用以指代將得益於用變異多肽(包含本發明之變異Fc區的多肽)治療之任何病狀,包括慢性及急性病症或疾病(例如,使患者易患特定病症之病理學病狀)。
如本文中所使用,術語「受體」係指能夠結合至少一種配位體之多肽。較佳受體為具有胞外配位體結合域及視情況其他域(例如,跨膜域、胞內域及/或膜錨)之細胞表面或可溶性受體。在本文中所描述之分析中評估之受體可為完整受體或其片段或衍生物(例如,包含與一或多種異源多肽融合之受體之結合域的融合蛋白)。此外,用於評估受體之結合性質的受體可存在於細胞中或經分離且視情況塗佈於分析培養盤或某一其他固相上或經直接標記且用作探針。
貓野生型 IgG
貓IgG為此項技術中熟知的且充分描述於例如Strietzel等人, 2014,
Vet Immunol Immunopathol., 第158 (3-4)卷, 第214-223頁中。在一個實施例中,貓IgG為IgG1
a。在另一實施例中,貓IgG為IgG1
b。在又一實施例中,貓IgG為IgG2。在一特定實施例中,貓IgG為IgG1
a。
IgG1
a、IgG1
b及IgG2之胺基酸及核酸序列亦為此項技術中所熟知的。
在一個實例中,本發明之IgG包含恆定域,例如CH1、CH2或CH3域,或其組合。在另一實施例中,本發明之恆定域包含Fc區,包括例如CH2或CH3域,或其組合。
在一特定實例中,野生型恆定域包含SEQ ID NO.:3中所闡述之胺基酸序列。在一些實施例中,野生型IgG恆定域係SEQ ID NO.:3之同系物、變異體、異構體或功能片段,但不含位置428或434之任何突變。各可能性代表本發明之各別實施例。
IgG恆定域亦包括具有與重鏈及/或輕鏈之胺基酸序列實質上類似之胺基酸序列的多肽。實質上相同的胺基酸序列在本文所定義為與比較胺基酸序列具有至少70%、75%、80%、85%、90%、、95%或99%一致性的序列,如藉由根據Pearson及Lipman,Proc. Natl. Acad. Sci. USA 85:2444-2448 (1988)之FASTA搜索法所測定。
本發明亦包括本文中所描述之編碼IgG或其部分之核酸分子。在一個實施例中,核酸可編碼包含例如CH1、CH2、CH3區或其組合之抗體重鏈。在另一實施例中,核酸可編碼包含例如VH區中之任一者或其部分,或VH CDR中之任一者,包括其任何變異體之抗體重鏈。本發明亦包括編碼抗體輕鏈之核酸分子,該抗體輕鏈包含例如CL區中之任一者或其部分、VL區中之任一者或其部分,或VL CDR中之任一者,包括其任何變異體。在某些實施例中,核酸編碼重鏈及輕鏈兩者或其部分。
SEQ ID NO.:3中闡述之野生型恆定域之胺基酸序列係由SEQ ID NO.:4中闡述之核酸序列編碼。
經修飾之貓 IgG
本申請案之本發明人發現,位置428或434之胺基酸殘基絲胺酸(Ser或S)經另一胺基酸取代出人意料地且未預期地增強了針對FcRn之親和力且延長了IgG之半衰期。如本文中所使用,術語位置428或位置434係指根據如Kabat中之EU索引編號的位置(Kabat等人, Sequences of Proteins of Immunological Interest, 第5版. Public Health Service, National Institutes of Health, Bethesda, Md. (1991))。
因此在一個實施例中,本發明提供一種經修飾之IgG,其包含:相對於野生型貓IgG恆定域,包含至少一個胺基酸取代之貓IgG恆定域,其中該取代處於根據如Kabat中之EU索引編號的胺基酸殘基428。位置428之絲胺酸可經任何其他胺基酸取代。舉例而言,位置428之絲胺酸可經以下取代:白胺酸(亦即,S428L)、天冬醯胺(亦即,S428N)、丙胺酸(亦即,S428A)、苯丙胺酸(亦即,S428F)、甘胺酸(亦即,S428G)、異白胺酸(亦即,S428I)、離胺酸(亦即,S428K)、組胺酸(亦即,S428H)、甲硫胺酸(亦即,S428M)、麩醯胺酸(亦即,S428Q)、精胺酸(亦即,S428R)、蘇胺酸(亦即,S428T)、纈胺酸(亦即,S428V)、色胺酸(亦即,S428W)、酪胺酸(亦即,S428Y)、半胱胺酸(亦即,S428C)、天冬胺酸(亦即,S428D)、麩胺酸(亦即,S428E)或脯胺酸(亦即S428P)。在一特定實施例中,取代係經白胺酸取代(亦即,S428L)。
在一特定實例中,本發明之突變恆定域包含SEQ ID NO.:1中所闡述之胺基酸序列。在一些實施例中,突變IgG恆定域係SEQ ID NO.:1之同系物、變異體、異構體或功能片段,但具有位置428之突變。各可能性代表本發明之各別實施例。
SEQ ID NO.:1中闡述之突變恆定域之胺基酸序列係由其對應突變核酸序列,例如SEQ ID NO.:4中闡述之核酸序列之突變形式編碼。
在另一實施例中,本發明提供一種經修飾之IgG,其包含:相對於野生型貓IgG恆定域,包含至少一個胺基酸取代之貓IgG恆定域,其中該取代處於根據如Kabat中之EU索引編號的胺基酸殘基434。位置434之絲胺酸可經任何其他胺基酸取代。舉例而言,位置434之絲胺酸可經以下取代:組胺酸(亦即,S434H)、天冬醯胺(亦即,S434N)、丙胺酸(亦即,S434A)、苯丙胺酸(亦即,S434F)、甘胺酸(亦即,S434G)、異白胺酸(亦即,S434I)、離胺酸(亦即,S434K)、白胺酸(亦即,S434L)、甲硫胺酸(亦即,S434M)、麩醯胺酸(亦即,S434Q)、精胺酸(亦即,S434R)、蘇胺酸(亦即,S434T)、纈胺酸(亦即,S434V)、色胺酸(亦即,S434W)、酪胺酸(亦即,S434Y)、半胱胺酸(亦即,S434C)、天冬胺酸(亦即,S434D)、麩胺酸(亦即,S434E)或脯胺酸(亦即,S434P)。在一特定實施例中,取代係經組胺酸取代(亦即,S434H)。
在一特定實例中,本發明之突變恆定域包含SEQ ID NO.:2中所闡述之胺基酸序列。在一些實施例中,突變IgG恆定域係SEQ ID NO.:2之同系物、變異體、異構體或功能片段,但具有位置434之突變。各可能性代表本發明之各別實施例。
SEQ ID NO.:2中闡述之突變恆定域之胺基酸序列係由其對應突變核酸序列,例如SEQ ID NO.:4中闡述之核酸序列之突變形式編碼。
在一些實施例中,貓IgG恆定域包含428及434位置之絲胺酸分別經白胺酸及組胺酸取代。
本發明之經修飾之IgG提供範圍介於約8天至約26天時間段的半衰期。在一個實施例中,本發明之經修飾之IgG提供約10、12、15、17、20、23或26天之半衰期。在一特定實施例中,本發明之經修飾之IgG提供大於10天的半衰期。
用於製備本發明之抗體分子的方法
用於製備抗體分子的方法為此項技術中熟知的且充分描述於美國專利8,394,925;8,088,376;8,546,543;10,336,818;及9,803,023及美國專利申請案公開案20060067930中,該等專利以全文引用之方式併入本文中。可使用熟習此項技術者已知的任何適合之方法、製程或技術。具有本發明之變異Fc區的抗體分子可根據此項技術中熟知的方法來產生。在一些實施例中,變異Fc區可與所選異源多肽,諸如抗體可變域或受體或配位體之結合域融合。
隨著分子生物學及重組技術方法之出現,熟習此項技術之人員可藉由重組方式產生抗體及抗體樣分子且藉此產生編碼在抗體之多肽結構中發現之特異性胺基酸序列的基因序列。此類抗體可藉由選殖編碼該等抗體之多肽鏈的基因序列或藉由直接合成該等多肽鏈及組裝合成鏈以形成針對特定抗原決定基及抗原決定子具有親和力之活性四聚(H2L2)結構來製備。此允許準備產生具有來自不同物種及來源之中和抗體之序列特徵的抗體。
無論抗體之來源如何,或其如何以重組方式構築,或其如何在活體外或活體內使用轉殖基因動物(實驗室或商業規模之大細胞培養物)、使用轉殖基因植物,或藉由在製程之任何階段不採用活生物體而直接進行化學合成來合成,所有抗體均具有整體類似的3維結構。此結構通常以H2L2形式提供且指代抗體通常包含兩條輕(L)胺基酸鏈及2條重(H)胺基酸鏈的事實。兩條鏈具有能夠與結構上互補之抗原目標交互的區。與該目標交互之區稱為「可變」或「V」區且其特徵在於具有不同抗原特異性之抗體的胺基酸序列不同。H或L鏈之可變區含有能夠特異性結合於抗原目標之胺基酸序列。
如本文中所使用,術語「抗原結合區」係指抗體分子之含有與抗原相互作用且向抗體賦予其針對抗原之特異性及親和力之胺基酸殘基的部分。抗體結合區包括保持抗原結合殘基之恰當構形所必需的「構架」胺基酸殘基。在提供抗原結合區之H或L鏈之可變區內為稱為「高變」之小序列,因為其在不同特異性抗體之間具有極高變異性。此類高變區亦稱為「互補決定區」或「CDR」區。此等CDR區造成抗體針對特定抗原決定子結構之基本特異性。
CDR表示可變區內之非相鄰胺基酸延伸,但與物種無關,已發現此等重要胺基酸序列在可變重鏈及輕鏈區內之位置在可變鏈之胺基酸序列內具有類似位置。所有抗體之可變重鏈及輕鏈各自具有三個彼此不相鄰的CDR區。在所有哺乳動物物種中,抗體肽含有恆定(亦即,高度保守性)及可變區,且在後者中存在CDR,且所謂的「構架區」由在重鏈或輕鏈之可變區內但在CDR之外的胺基酸序列構成。
本發明進一步提供包括上文所描述之核酸中之至少一者的載體。因為遺傳密碼係簡併的,所以可使用超過一個密碼子編碼特定胺基酸。使用遺傳密碼,可鑑別出一或多種不同核苷酸序列,其中之每一者將能夠編碼胺基酸。特定寡核苷酸實際上將構成實際編碼序列之機率可藉由考慮異常鹼基配對關係及在表現抗體或部分之真核或原核細胞中實際上使用(編碼特定胺基酸的)特定密碼子的頻率來估算。Lathe等人,183 J. Molec. Biol. 1-12(1985)揭示了此類「密碼子使用規則」。使用Lathe之「密碼子使用規則」,可鑑別出含有理論上能夠編碼貓IgG序列之「最可能」核苷酸序列的單核苷酸序列或核苷酸序列之集合。亦預期編碼用於本發明之區的抗體亦可藉由使用產生本文中所描述之抗體及肽之變異體的標準分子生物技術改變現有抗體基因來提供。此類變異體包括(但不限於)抗體或肽之胺基酸序列的缺失、添加及取代。
舉例而言,一類取代為保守性胺基酸取代。此類取代為貓抗體肽中之既定胺基酸經另一具有類似特徵之胺基酸取代的彼等取代。通常視為保守性取代的是脂族胺基酸Ala、Val、Leu及lie中之一個置換成另一個;羥基殘基Ser及Thr之互換;酸性殘基Asp及Glu之交換;醯胺殘基Asn與Gin之間的取代;鹼性殘基Lys及Arg之交換;芳族殘基Phe、Tyr等中之置換。關於那些胺基酸變化有可能在表現型上沉默之指南發現於Bowie等人,247
Science1306-10 (1990)。
變異貓抗體或肽可能為全功能或可能在一或多個活動中缺乏功能。全功能變異體通常僅含有保守性變型或非關鍵殘基或非關鍵區中之變型。功能變異體亦可含有使得功能無變化或不明顯變化的類似胺基酸取代。替代地,此類取代可能在一定程度上對功能產生正面或負面影響。非功能性變異體通常含有一或多種非保守性胺基酸取代、缺失、插入、反轉或截短,或關鍵殘基或關鍵區中之取代、插入、反轉或缺失。
可藉由此項技術中已知之方法(諸如定點突變誘發或丙胺酸掃描突變誘發)鑑別出功能必需的胺基酸。Cunningham等人,244
Science1081-85 (1989)。後一程序在分子中之每個殘基處引入單丙胺酸突變。隨後測試所得突變分子之生物活性,諸如抗原決定基結合或活體外ADCC活性。對於配位體-受體結合關鍵之位點亦可藉由結構分析(諸如結晶學)、核磁共振或光親和性標記來測定。Smith等人,224
J. Mol. Biol.899-904 (1992);de Vos等人, 255
Science306-12 (1992)。
此外,多肽通常含有除二十種「天然存在」胺基酸以外之胺基酸。此外,包括末端胺基酸之許多胺基酸可藉由天然過程(諸如加工及其他轉譯後修飾)或藉由此項技術中熟知的化學修飾技術來修飾。已知修飾包括(但不限於)乙醯化、醯化、ADP-核糖基化、醯胺化、黃素之共價附接、血紅素部分之共價附接、核苷酸或核苷酸衍生物之共價附接、脂質或脂質衍生物之共價附接、磷脂醯肌醇之共價附接、交聯、環化、雙硫鍵形成、去甲基化、共價交聯之形成、胱胺酸之形成、焦麩胺酸之形成、甲醯化、伽瑪羧化、糖基化、GPI錨形成、羥基化、碘化、甲基化、豆蔻醯化、氧化、蛋白水解加工、磷酸化、異戊烯化、外消旋化、硒化、硫酸化、轉移RNA介導之胺基酸添加至蛋白質(諸如精氨醯化)及泛蛋白化。此類修飾已為熟習此項技術者所熟知且非常詳細地描述於科學文獻中。舉例而言,幾種特定地常見修飾糖基化、脂質附接、硫酸化、麩胺酸殘基之伽瑪羧化、羥基化及ADP核糖基化描述於大多數基礎本文中,諸如Proteins-Structure and Molecular Properties (第2版,T. E. Creighton, W. H. Freeman & Co., N.Y., 1993)。可獲得關於此主題之許多詳細的綜述,諸如根據Wold,Posttranslational Covalent Modification of proteins, 1-12 (Johnson編., Academic Press, N.Y., 1983);Seifter等人. 182
Meth. Enzymol. 626-46 (1990);及Rattan等人,663
Ann. NY Acad. Sci. 48-62 (1992)。
在另一態樣中,本發明提供抗體衍生物。抗體之「衍生物」含有通常並非蛋白質之一部分的其他化學部分。蛋白質之共價修飾包括於本發明之範疇內。可藉由使抗體之目標胺基酸殘基與有機衍生劑反應將此類修飾引入分子中,該有機衍生劑能夠與所選側鏈或末端殘基反應。舉例而言,用此項技術中熟知的雙官能性試劑進行衍生化適用於將抗體或片段與水不可溶載體基質或與其他巨分子載劑交聯。
衍生物亦包括經標記的放射性標記之單株抗體。舉例而言,放射性碘(251、1311)、碳(4C)、硫(35S)、銦、氚(H
3)或類似者;單株抗體與生物素或抗生素蛋白、與酶(諸如辣根過氧化物酶、鹼性磷酸酶、β-D-半乳糖苷酶、葡萄糖氧化酶、澱粉酶、羧酸脫水酶、乙醯膽鹼酯酶、溶菌酶、蘋果酸脫氫酶或葡萄糖6-磷酸酯脫氫酶)之結合物;以及單株抗體與生物發光劑(諸如螢光素酶)、靜默變化劑(諸如吖啶酯)或螢光劑(諸如藻膽蛋白)之結合物。
本發明之另一衍生物雙官能性抗體為藉由組合兩種單獨抗體之識別兩種不同抗原基團的部分而產生的雙特異性抗體。此可藉由交聯或重組技術來實現。另外,各部分可添加至抗體或其部分中以增加活體內半衰期(例如,藉由延長達至血流清除之時間)。此類技術包括例如添加PEG部分(亦稱為聚乙二醇化),且為此項技術中熟知的。參見美國專利申請公開案第20030031671號。
在一些實施例中,將編碼主題抗體之核酸直接引入至宿主細胞中,且在足以誘導編碼之抗體表現之條件下培育細胞。在主題核酸已引入至細胞中之後,典型地通常在37℃下(有時在選擇下)培育細胞約1至24小時的時間段以便允許抗體表現。在一個實施例中,抗體經分泌於細胞生長之培養基之上清液中。傳統上,在鼠類雜交瘤株中產生呈天然分子形式之單株抗體。除了彼技術之外,本發明提供抗體之重組DNA表現。此允許在所選宿主物種中產生抗體,以及一系列抗體衍生物及融合蛋白質。
編碼本發明之至少一種抗體、部分或多肽之核酸序列可根據習知技術與載體DNA重組,該等技術包括用於連接之平端式或交錯端式末端、提供適當末端之限制酶消化、黏合末端視需要之填充、避免不當連接之鹼性磷酸酶處理及利用適當連接酶之連接。此類操縱之技術係藉由例如Maniatis等人, MOLECULAR CLONING, LAB. MANUAL, (Cold Spring Harbor Lab. Press, NY, 1982 及1989)及上述之Ausubel等人,1993揭示,可用於構築編碼抗體分子或其抗原結合區之核酸序列。
若諸如DNA之核酸分子含有含轉錄及轉譯調節資訊之核苷酸序列且此類序列「可操作地連接」至編碼多肽之核苷酸序列,則該核酸分子稱為「能夠表現」該多肽。可操作鍵聯為其中視圖表現之調節DNA序列及DNA序列以允許基因表現為可回收量的肽或抗體部分之方式連接的鍵聯。基因表現所需之調節區之精確性質可能因不同生物體而不同,如類似技術中所熟知。參見例如上述之Sambrook等人,2001;上述之Ausubel等人,1993。
因此,本發明涵蓋原核或真核細胞中之抗體或肽之表現。適合之宿主包括細菌或真核宿主,包括活體內或原位的細菌、酵母菌、昆蟲、真菌、鳥類及哺乳動物細胞,或哺乳動物、昆蟲、鳥類或酵母菌來源之宿主細胞。哺乳動物細胞或組織可屬於人類靈長類、倉鼠、兔、嚙齒類動物、乳牛、豬綿羊、馬、山羊、狗或貓來源。亦可使用此項技術中已知的任何其他適合之哺乳動物細胞。
在一個實施例中,本發明之核苷酸序列將併入至能夠在接受者宿主中自發複製的質體或病毒載體中。廣泛多種載體中之任一者可用於此目的。參見例如上述之Ausubel等人,1993。選擇特定質體或病毒載體之重要因素包括:可自不含有載體之彼等接受者細胞中識別且選擇出含有載體之接受者細胞的容易性;特定宿主中所需要的載體複本數目;及是否期望能夠在不同物種之宿主細胞之間「穿梭」載體。
此項技術中已知之實例原核載體包括質體,諸如能夠在大腸桿菌中複製之彼等質體(諸如(例如)pBR322、CoIE1、pSC101、pACYC 184、.pi.vX)。舉例而言,此類質體係藉由上述之Maniatis等人,1989;上述之Ausubel等人,1993揭示。芽孢桿菌屬質體包括pC194、pC221、pT127等。此類質體係藉由Gryczan揭示於THE MOLEC BIO. OF THE BACILLI 307-329 (Academic Press, NY, 1982)中。適合的鏈黴菌屬質體包括p1J101 (Kendall等人, 169 J. Bacteriol. 4177-83 (1987))及鏈黴菌屬噬菌體,諸如phLC31 (Chater等人於SIXTH INT'L SYMPOSIUM ON ACTINOMYCETALES BIO. 45-54 (Akademiai Kaido, Budapest, Hungary 1986)中)。假單胞菌屬質體經綜述於John等人, 8 Rev. Infect. Dis. 693-704 (1986);lzaki, 33 Jpn. J. Bacteriol. 729-42 (1978);及上述之Ausubel等人, 1993中。
替代地,適用於表現編碼抗體或肽之cDNA的基因表現元件包括(但不限於)(a)病毒轉錄啟動子及其強化子元件,諸如SV40早期啟動子(Okayama等人, 3 Mol. Cell. Biol. 280 (1983))、勞氏肉瘤病毒LTR (Gorman等人,79 Proc. Natl. Acad. Sci., USA 6777 (1982))及莫洛尼鼠類白血病病毒LTR (Grosschedl等人, 41 Cell 885 (1985));(b)剪接區及聚腺苷酸化位點,諸如衍生自SV40晚期區之彼等(Okayarea等人,1983);及(c)諸如SV40中之聚腺苷酸化位點(Okayama等人,1983)。
可如Weidle等人,51 Gene 21 (1987)所描述,使用SV40早期啟動子及其強化子、小鼠免疫球蛋白H鏈啟動子強化子、SV40晚期區mRNA剪接、兔S-血球蛋白插入序列、免疫球蛋白及兔S-血球蛋白聚腺苷酸化位點及SV40聚腺苷酸化元件作為表現元件來表現免疫球蛋白cDNA基因。對於由部件cDNA、部件基因體DNA構成之免疫球蛋白基因(Whittle等人, 1 Protein Engin. 499 (1987)),轉錄啟動子可為人類細胞巨大病毒,啟動子強化子可為細胞巨大病毒及小鼠/人類免疫球蛋白,且mRNA剪接及聚腺苷酸化區可為天然染色體免疫球蛋白序列。
在一個實施例中,針對嚙齒類動物細胞中之cDNA基因表現,轉錄啟動子為病毒LTR序列,轉錄啟動子強化子為小鼠免疫球蛋白重鏈強化子及病毒LTR強化子中之任一者或兩者,剪接區含有大於31 bp之內含子,且聚腺苷酸化及轉譯終止區衍生自與將合成之免疫球蛋白鏈相對應的天然染色體序列。在其他實施例中,編碼其他蛋白質之cDNA序列與上文列舉之表現元件組合以實現哺乳動物細胞中之蛋白質表現。
各融合基因可組裝於表現載體中或插入至表現載體中。能夠表現免疫球蛋白鏈基因產物之接受者細胞隨後僅傳染有肽或H或L鏈編碼基因,或共轉染有H及L鏈基因。經轉染之受體細胞在准許合併基因之表現的條件下培養且自培養物回收表現的免疫球蛋白鏈或完整抗體或片段。
在一個實施例中,編碼肽或H及L鏈之融合基因或其部分經組裝於個別表現載體中,該等表現載體隨後用以共轉染接受者細胞。替代地,編碼H及L鏈之融合基因可組裝於相同表現載體上。對於表現載體之轉染及抗體之產生,接受者細胞株可為骨髓瘤細胞。骨髓瘤細胞可合成、組裝及分泌由經傳染之免疫球蛋白基因編碼之免疫球蛋白且具有使免疫球蛋白糖基化之機制。骨髓瘤細胞可在培養物中或在小鼠之腹腔中生長,其中分泌之免疫球蛋白可自腹水流體中獲得。其他適合之接受者細胞包括淋巴細胞,諸如貓或非貓來源之B淋巴球;貓或非貓來源之融合瘤細胞;或物種間的異種融合瘤細胞。
攜載本發明之抗體構築體或多肽的表現載體可藉由多種適合之方式中之任一者引入至適當宿主細胞中,該等方式包括生物化學方式,諸如轉化、轉染、共軛、原生質體融合、磷酸鈣-沈澱及施用諸如二乙胺基乙基(DEAE)聚葡糖的聚陽離子;及機械方式,諸如電穿孔、直接顯微注射及微彈轟擊。Johnston等人,240
Scienc e1538 (1988)。
對於免疫球蛋白H及L鏈之產生,酵母菌可提供優於細菌之明顯優勢。酵母菌會進行包括糖基化之轉譯後肽修飾。目前存在多種利用強啟動子序列及高質體複本數之重組DNA策略。該等強啟動子序列及高質體複本數可用於在酵母菌中產生所需蛋白質。酵母菌識別經選殖哺乳動物基因產物之前導序列且分泌攜帶前導序列之肽(亦即前肽)。Hitzman等人, 11th Int'l Conference on Yeast, Genetics & Molec. Biol. (Montpelier, France, 1982)。
可常規地評估酵母菌基因表現系統之肽、抗體、其片段及區的產生量、分泌量及穩定性。當酵母菌在富含葡萄糖之培養基中生長時,可利用一系列酵母菌基因表現系統中之任一者,該等系統併入了來自編碼大量產生之糖分解酶之有效表現基因的啟動子及終止元件。已知糖分解基因亦可提供極有效的轉錄控制信號。舉例而言,可利用磷酸甘油酸激酶(PGK)基因之啟動子及終止子信號。可採取多種途徑來評估用於在酵母菌中表現經選殖免疫球蛋白cDNA之最優表現質體。參見第II卷DNA Cloning, 45-66, (Glover編) IRL Press, Oxford, UK 1985)。
細菌菌株亦可用作用以產生本發明所述之抗體分子或肽的宿主。將含有衍生自與宿主細胞相容之物種之複製子及控制序列的質體載體結合此等細菌宿主使用。載體通常攜帶複製位點以及能夠在轉型細胞中提供表型選擇之特定基因。可採用多種途徑來評估用於在細菌中產生由經選殖免疫球蛋白cDNA編碼之抗體、片段及區或抗體鏈之表現質體(參見上述之Glover, 1985;上述之Ausubel, 1993;上述之Sambrook, 2001;Colligan等人編. Current Protocols in Immunology, John Wiley & Sons, NY, N.Y. (1994-2001);Colligan等人編. Current Protocols in Protein Science, John Wiley & Sons, NY, N.Y. (1997-2001))。
宿主哺乳動物細胞可活體外或活體內生長。哺乳動物細胞提供針對免疫球蛋白蛋白分子之轉譯後修飾,包括前導肽移除、H及L鏈之摺疊及組裝、抗體分子之糖基化及功能性抗體蛋白質之分泌。除了上文所描述之淋巴來源之細胞之外,可用作產生抗體蛋白之宿主的哺乳動物細胞包括纖維母細胞來源之細胞,諸如Vero (ATCC CRL 81)或CHO-K1 (ATCC CRL 61)細胞。許多載體系統可用於在哺乳動物細胞中表現選殖肽H及L鏈基因(參見上述之Glover,1985)。可遵循不同途徑以獲得完全H2L2抗體。可能在相同細胞中共表現H及L鏈以實現H及L鏈胞內締合及鍵聯成完全四聚體H2L2抗體及/或肽。可藉由在相同宿主中使用相同或不同的質體來進行共表現。H及L鏈及/或肽之基因可置放於相同質體中,隨後將該質體轉染至細胞中,藉此直接選擇表現該兩條鏈之細胞。替代地,細胞可首先轉染有編碼一條鏈(例如L鏈)之質體,接著使所得細胞株轉染有含第二可選標記之H鏈質體。經由任一途徑產生肽及/或H2L2分子之細胞株可轉染有編碼其他肽複本、H、L或H加L鏈以及前他可選標記之質體以產生具有增強特性之細胞株,諸如更高的產生經組裝H2L2抗體分子或經轉染細胞株之穩定性增強。
為長期、高產率產生重組型抗體,可使用穩定表現。舉例而言,可對穩定表現抗體分子之細胞株進行工程改造。勝於使用含有病毒複製起點之表現載體,宿主細胞可用免疫球蛋白表現卡匣及可選標記轉化。在引入外源DNA之後,可使經工程改造之細胞在富集培養基中生長1至2天,且接著轉換成選擇性培養基。重組型質體中之可選標記賦予對選擇之抵抗性且允許細胞將質體穩定整合至染色體中並生長以形成又可選殖且擴展至細胞株中的焦點。此類經工程改造之細胞株可特別適用於篩選及評估直接地或間接地與抗體分子相互作用的化合物/組分。
一旦產生本發明抗體,則可藉由此項技術中已知的用於純化免疫球蛋白分子之任何方法,例如藉由層析法(例如離子交換、親和力、針對蛋白質A之後的特定抗原之特定親和力及篩分管柱層析法)、離心、差異溶解性或藉由用於純化蛋白質之任何其他標準技術來將其純化。在許多實施例中,抗體由細胞分泌至培養基中且自培養基中收集。
在另一態樣中,本發明提供一種抗體,其包含:相對於野生型貓IgG恆定域,包含至少一個胺基酸取代之貓IgG恆定域,其中該取代處於胺基酸殘基428、434或其組合。在一個實施例中,取代為位置428之絲胺酸經白胺酸取代(S428L)。在另一實施例中,取代為位置434之絲胺酸經組胺酸取代(S434H)。
具有取代之抗體可為熟習此項技術者已知的任何適合之抗體。在一個實例中,抗體為抗IL31抗體。在另一實例中,抗體為抗NGF抗體。在另一實例中,抗體為抗TGFβ抗體。
本文中所描述之不含取代之抗IL31抗體為此項技術中所熟知的且充分描述於例如美國專利10,526,405;10,421,807;9,206,253;及8,790,651中。另外,本文中所描述之不含取代之抗NGF抗體亦為此項技術中所熟知的且充分描述於例如美國專利10,125,192;10,093,725;9,951,128;9,617,334;及9,505,829中。此外,不具有本文所描述之取代的抗TGFβ抗體亦為此項技術中眾所周知的且充分描述於例如美國專利申請案63/248,679及63/036,092以及PCT國際專利申請案PCT/US2021/036347中。
在一個實施例中,本發明之抗IL31抗體(亦即,具有取代之抗體)減少、抑制或中和IL-31介導之瘙癢或過敏性病狀。在另一實施例中,本發明之抗IL31抗體減少、抑制或中和貓之IL-31活性。
抗IL31抗體之VL、VH及CDR序列為此項技術中所熟知的且充分描述於例如美國專利10,526,405;10,421,807;9,206,253;及8,790,651中。在一個實例中,本發明之抗IL31抗體可包括以下互補決定區(CDR)序列中之至少一者:SEQ ID NO:15之可變重鏈(VH)-CDR1、SEQ ID NO:16之VH-CDR2、SEQ ID NO:17之VH-CDR3、SEQ ID NO:20之可變輕鏈(VL)-CDR1、SEQ ID NO:21之VL-CDR2及SEQ ID NO:22之VL-CDR3。在一些實施例中,本發明之抗IL31抗體可包括本文中所描述之至少一種CDR。
在一個實施例中,本發明之抗IL31抗體可包括包含SEQ ID NO:19中所闡述之胺基酸序列的可變輕鏈。在另一實施例中,本發明之抗IL31抗體可包括包含SEQ ID NO:14中所闡述之胺基酸序列的可變重鏈。
在一個實施例中,本發明之突變抗NGF抗體(亦即具有取代之抗體)減少、抑制或中和動物中之NGF活性,及/或增強抑制NGF結合於Trk A及p75之能力,以便治療NGF介導之疼痛或病狀。
抗NGF抗體之VL、VH及CDR序列亦為此項技術中所熟知的且充分描述於例如美國專利10,125,192;10,093,725;9,951,128;9,617,334;及9,505,829中。在一個實例中,本發明之抗NGF抗體可包括以下互補決定區(CDR)序列中之至少一者:SEQ ID NO:24之可變重鏈(VH)-CDR1、SEQ ID NO:25之VH-CDR2、SEQ ID NO:26之VH-CDR3、SEQ ID NO:28之可變輕鏈(VL)-CDR1、SEQ ID NO:29之VL-CDR2及SEQ ID NO:30之VL-CDR3。
在另一實例中,本發明之抗NGF抗體可包括以下互補決定區(CDR)序列中之至少一者:SEQ ID NO:32之可變重鏈(VH)-CDR1、SEQ ID NO:33之VH-CDR2、SEQ ID NO:34之VH-CDR3、SEQ ID NO:36之可變輕鏈(VL)-CDR1、SEQ ID NO:37之VL-CDR2及SEQ ID NO:38之VL-CDR3。
在一個實施例中,本發明之抗NGF抗體可包括可變輕鏈,該可變輕鏈包含SEQ ID NO:27或35中所闡述之胺基酸序列。
在另一實施例中,本發明之抗NGF抗體可包括可變重鏈,該可變重鏈包含SEQ ID NO:23或31中所闡述之胺基酸序列之可變序列。
在一個實施例中,本發明之抗TGFβ抗體(亦即,具有取代之抗體)減少、抑制或中和TGFβ介導之疾病或病況,例如慢性腎病。在另一實施例中,本發明之抗TGFβ抗體減少、抑制或中和貓之TGFβ活性。本發明之抗TGFβ抗體可結合至TGFβ1、TGFβ2、TGFβ3或其組合。舉例而言,在一個實施例中,本發明之抗TGFβ抗體結合至TGFβ1。在另一實施例中,本發明之抗TGFβ抗體結合至TGFβ2。在另一實施例中,本發明之抗TGFβ抗體結合至TGFβ3。在又一實施例中,本發明之抗TGFβ抗體結合至TGFβ1、TGFβ2、TGFβ3或其組合。
抗TGFβ抗體之VL、VH及CDR序列亦為此項技術中眾所周知的且充分描述於例如美國專利申請案63/036,092及63/248,679以及PCT國際專利申請案PCT/US2021/036347中。在一個實例中,本發明之抗TGFβ抗體可包括以下互補決定區(CDR)序列之組合中的至少一者:(1) ZTS-310:SEQ ID NO:39之可變重鏈(VH)-CDR1、SEQ ID NO:40之VH-CDR2、SEQ ID NO:41之VH-CDR3、SEQ ID NO:42之可變輕鏈(VL)-CDR1、SEQ ID NO:43之VL-CDR2及SEQ ID NO:44之VL-CDR3;或
(2) ZTS-120-1:SEQ ID NO:49之可變重鏈(VH)-CDR1、SEQ ID NO:50之VH-CDR2、SEQ ID NO:51之VH-CDR3、SEQ ID NO:52之可變輕鏈(VL)-CDR1、SEQ ID NO:53之VL-CDR2及SEQ ID NO:54之VL-CDR3;或
(3) ZTS-120-2:SEQ ID NO:59之VH-CDR1、SEQ ID NO:60之VH-CDR2、SEQ ID NO:61之VH-CDR3、SEQ ID NO:62之VL-CDR1、SEQ ID NO:63之VL-CDR2及SEQ ID NO:64之VL-CDR3;或
(4) ZTS-120-3:SEQ ID NO:69之VH-CDR1、SEQ ID NO:70之VH-CDR2、SEQ ID NO:71之VH-CDR3、SEQ ID NO:72之VL-CDR1、SEQ ID NO:73之VL-CDR2及SEQ ID NO:74之VL-CDR3;或
(5)ZTS-120-4:SEQ ID NO:79之VH-CDR1、SEQ ID NO:80之VH-CDR2、SEQ ID NO:81之VH-CDR3、SEQ ID NO:82之VL-CDR1、SEQ ID NO:83之VL-CDR2及SEQ ID NO:84之VL-CDR3;或
(6) ZTS-120-5:SEQ ID NO:89之VH-CDR1、SEQ ID NO:90之VH-CDR2、SEQ ID NO:91之VH-CDR3、SEQ ID NO:92之VL-CDR1、SEQ ID NO:93之VL-CDR2及SEQ ID NO:94之VL-CDR3;或
(7) ZTS-120-6:SEQ ID NO:99之VH-CDR1、SEQ ID NO:100之VH-CDR2、SEQ ID NO:101之VH-CDR3、SEQ ID NO:102之VL-CDR1、SEQ ID NO:103之VL-CDR2及SEQ ID NO:104之VL-CDR3;或
(8) ZTS-120-7:SEQ ID NO:109之VH-CDR1、SEQ ID NO:110之VH-CDR2、SEQ ID NO:111之VH-CDR3、SEQ ID NO:112之VL-CDR1、SEQ ID NO:113之VL-CDR2及SEQ ID NO:114之VL-CDR3;或
(9) ZTS-120-8:SEQ ID NO:119之VH-CDR1、SEQ ID NO:120之VH-CDR2、SEQ ID NO:121之VH-CDR3、SEQ ID NO:122之VL-CDR1、SEQ ID NO:123之VL-CDR2及SEQ ID NO:124之VL-CDR3;或
(10) ZTS-120-9:SEQ ID NO:129之VH-CDR1、SEQ ID NO:130之VH-CDR2、SEQ ID NO:131之VH-CDR3、SEQ ID NO:132之VL-CDR1、SEQ ID NO:133之VL-CDR2及SEQ ID NO:134之VL-CDR3。
在一些實施例中,本發明之抗TGFβ抗體可包括本文所描述之至少一個CDR。
在一個實施例中,本發明之抗TGFβ抗體可包括包含以下中闡述之胺基酸序列的可變重鏈:SEQ ID NO:45 (ZTS-310)、SEQ ID NO:55 (ZTS-120-1)、SEQ ID NO:65 (ZTS-120-2)、SEQ ID NO:75 (ZTS-120-3)、SEQ ID NO:85 (ZTS-120-4)、SEQ ID NO:95 (ZTS-120-5)、SEQ ID NO:105 (ZTS-120-6)、SEQ ID NO:115 (ZTS-120-7)、SEQ ID NO:125 (ZTS-120-8)或SEQ ID NO:135 (ZTS-120-9)。
在另一實施例中,本發明之抗TGFβ抗體可包括包含以下中闡述之胺基酸序列的可變輕鏈:SEQ ID NO:47 (ZTS-310)、SEQ ID NO:57 (ZTS-120-1)、SEQ ID NO:67 (ZTS-120-2)、SEQ ID NO:77 (ZTS-120-3)、SEQ ID NO:87 (ZTS-120-4)、SEQ ID NO:97 (ZTS-120-5)、SEQ ID NO:107 (ZTS-120-6)、SEQ ID NO:117 (ZTS-120-7)、SEQ ID NO:127 (ZTS-120-8)或SEQ ID NO:137 (ZTS-120-9)。
醫藥學及獸醫學應用
本發明亦提供一種醫藥組合物,其包含本發明之分子及一或多種醫藥學上可接受之載劑。更特定言之,本發明提供一種醫藥組合物,其包含醫藥學上可接受之載劑或稀釋劑及作為活性成分的本發明之抗體或肽。
「醫藥學上可接受之載劑」包括對於以所採用劑量及濃度暴露於其中之細胞或動物為無毒的任何賦形劑。醫藥組合物可包括一種或額外治療劑。
「醫藥學上可接受」係指彼等化合物、材料、組合物及/或劑型在合理醫學判斷之範疇內,適於與動物之組織接觸而無過度毒性、刺激、過敏反應或其他問題併發症,與合理的效益/風險比相稱。
醫藥學上可接受之載劑包括溶劑、分散介質、緩衝液、包衣、抗菌劑及抗真菌劑、潤濕劑、防腐劑、傢伙(buggers)、螯合劑、抗氧化劑、等張劑及吸收延遲劑。
醫藥學上可接受之載劑包括水;生理食鹽水;磷酸鹽緩衝鹽水;右旋糖;甘油;諸如乙醇及異丙醇之醇;磷酸、檸檬酸及其他有機酸;抗壞血酸;低分子量(少於約10個殘基)多肽;諸如血清白蛋白、明膠或免疫球蛋白之蛋白質;諸如聚乙烯吡咯啶酮之親水性聚合物;諸如甘胺酸、麩醯胺酸、天冬醯胺、精胺酸或離胺酸之胺基酸;單醣、雙醣及其他包括葡萄糖、甘露糖或糊精之碳水化合物;EDTA;諸如鈉之成鹽相對離子;及/或諸如TWEEN、聚乙二醇(PEG)及PLURONICS之非離子界面活性劑;諸如糖、多元醇(諸如甘露醇及山梨醇)及氯化鈉之等張劑;以及其組合。
本發明之醫藥組合物可以多種方式調配,包括例如液體、半固體及固體劑型,諸如液體溶液(例如可注射溶液及可輸注溶液)、分散液或懸浮液、脂質體、栓劑、錠劑、丸劑或散劑。在一些實施例中,組合物係呈可注射或可輸注溶液形式。組合物可呈適於靜脈內、動脈內、肌肉內、皮下、非經腸、經黏膜、經口、局部或經皮投與之形式。組合物可調配為立即、控制、延長或延遲釋放組合物。
本發明之組合物可以單獨的治療劑形式或與其他治療劑組合之形式投與。其可單獨投與,但通常與基於所選投藥途徑及標準醫藥實踐選擇的醫藥學載劑一起投與。本文所揭示之抗體之投藥可藉由任何適合之手段進行,包括非經腸注射(諸如腹膜內、皮下或肌肉內注射)、經口,或藉由將抗體(典型地攜載於醫藥調配物中)局部投與至呼吸道表面。局部投與至呼吸道表面可藉由鼻內投與(例如藉由使用滴管、拭子或吸入器)來進行。抗體局部投與至呼吸道表面亦可藉由吸入投與,諸如藉由形成呈氣霧懸浮液形式的含有抗體之醫藥調配物之可吸入粒子,且接著使個體吸入該等可吸入粒子來進行。用於投與醫藥調配物之可吸入粒子的方法及裝置為吾人所熟知的,且可採用任何習知技術。
在一些所需實施例中,抗體藉由非經腸注射來投與。對於非經腸投與,抗體或分子可結合醫藥學上可接受之非經腸媒劑調配為溶液、懸浮液、乳液或凍乾粉形式。舉例而言,媒劑可為抗體溶液或其溶解於可接受之載劑(諸如水性載劑)中的混合物,此類媒劑為水、生理鹽水、林格氏溶液、右旋糖溶液、海藻糖或蔗糖溶液或5%血清白蛋白、0.4%生理鹽水、0.3%甘胺酸及類似者。亦可使用脂質體及非水性媒劑,諸如非揮發性油。此等溶液為無菌的且通常不含顆粒物質。此等組合物可藉由習知熟知滅菌技術來滅菌。組合物可含有醫藥學上可接受之輔助物質,如大致生理條件所需要,諸如pH調節劑及緩衝劑、毒性調節劑及其類似者,例如乙酸鈉、氯化鈉、氯化鉀、氯化鈣、乳酸鈉等。此等調配物中之抗體濃度可廣泛變化,例如自小於約0.5重量%,通常為或至少約為1重量%至高達15重量%或20重量%,且將根據所選擇之特定投藥模式主要基於液體體積、黏度等來選擇。媒劑或凍乾粉可含有維持等張性之添加劑(例如氯化鈉、甘露醇)及維持化學穩定性之添加劑(例如緩衝液及防腐劑)。調配物藉由常用技術來滅菌。用於製備非經腸可投與組合物之實際方法將為熟習此項技術者已知或顯而易見,且其更詳細地描述於例如REMINGTON'S PHARMA. SCI. (第15版, Mack Pub. Co., Easton, Pa., 1980)中。
本發明之抗體或分子可凍乾以便儲存且在使用之前在適合之載劑中復原。此技術已顯示對習知免疫球蛋白有效。可採用任何適合之凍乾及復原技術。熟習此項技術者應瞭解,凍乾及復原可引起不同程度的抗體活性損失且可必須調整使用水準以補償。可投與含有本發明抗體或其混合物之組合物以預防現有疾病之復發及/或治療性治療現有疾病。適合之醫藥學載劑描述於最近版本之雷明頓氏醫藥科學(此技術領域中之標準參考本文)中。在治療性應用中,向已經患有疾病之個體投與足以治癒或至少部分地遏制或減輕疾病及其併發症之量的組合物。
用於治療如本文所描述之病狀或疾病的本發明之組合物的有效劑量視許多不同因素而變化,該等因素包括例如但不限於特定藥劑之藥效學特徵及其投藥模式及途徑;目標位點;動物之生理狀態;所投與之其他藥物;治療為預防性的抑或治療性的;接受者之年齡、健康狀況及體重;症狀之性質及程度、並行治療之類別、治療頻率及所需效果。
單次或多次投與組合物可以在治療獸醫所選之劑量及模式下進行。在任何情況下,醫藥調配物應提供足以有效治療個體之量的一或多種本發明抗體。在一些實施例中,組合物係兩個月一次、三個月一次、四個月一次、五個月一次、六個月一次或七個月一次地進行投與。
治療劑量可使用熟習此項技術者已知之常規方法來滴定以使安全性及功效最佳化。
本發明之醫藥組合物可包括「治療有效量」。「治療有效量」係指在所需劑量及時間段下,有效達成所需治療結果之量。治療有效量之分子可根據諸如個體之疾病病況、年齡、性別及體重,及分子在個體中引起所需反應之能力的因素而變化。治療有效量亦為分子之治療有益效應超過其任何毒性或有害效應的量。
在另一態樣中,本發明之組合物可用於例如治療貓之各種疾病及病症。如本文中所使用,術語「治療(treat/treatment)」係指治療性治療,包括防治性或預防性措施,其中目標係預防或減緩(減輕)非所要的與疾病或病狀相關之生理變化。不論可偵測或不可偵測,有益的或所需的臨床結果包括(但不限於)症狀緩解、疾病或病狀之程度減弱、疾病或病狀穩定(亦即,其中疾病或病狀不再惡化)、疾病或病狀之進程延遲或減緩、疾病或病狀改善或緩和及疾病或病狀緩解(不論部分或總體)。需要治療之彼等者包括已患有該疾病或病狀以及易於患有該疾病或病狀之彼等者或應預防該疾病或病狀之彼等者。
具有本發明之突變分子之組合物可用於治療任何適合之疾病或病症。舉例而言,本發明之突變抗IL31抗體可用於治療IL-31介導之瘙癢或過敏性病狀。IL-31介導之瘙癢病狀之實例包括例如但不限於異位性皮膚炎、濕疹、牛皮癬、硬皮病及瘙癢性皮炎。IL-31介導之過敏性病狀之實例包括例如但不限於過敏性皮炎、夏季濕疹、蕁麻疹、馬氣喘病、發炎性呼吸道疾病、復發性呼吸道阻塞、氣管過度反應、慢性阻塞性肺部疾病及由自體免疫引起之發炎過程。
本發明之突變抗NGF抗體可用於治療NGF介導之疼痛或病狀。疼痛之實例包括例如但不限於慢性疼痛、發炎性疼痛、術後切口疼痛、神經痛、骨折疼痛、骨質疏鬆性骨折疼痛、疱疹後神經痛、癌症痛、由燒傷引起之疼痛、與傷口相關之疼痛、與創傷相關之疼痛、神經痛、與肌肉骨骼病症相關之疼痛、類風濕性關節炎、骨關節炎、僵直性脊椎炎、血清陰性(非類風濕性)關節病、非關節風濕病、關節周圍病症或周邊神經病變。在一特定實施例中,疼痛為骨關節炎疼痛。
本發明之突變抗TGFβ抗體可用於治療TGFβ介導之疾病或病況。TGFβ介導之疾病或病況之實例包括例如但不限於慢性腎病。
本說明書中引用之所有專利及文獻參考以全文引用之方式併入本文中。
提供以下實例以補充先前揭示內容且提供對本文所描述之主題的較佳理解。此等實例不應視為限制所描述之主題。應理解,本文所描述之實例及實施例僅用於說明之目的,且鑒於其各種修改或改變對於熟習此項技術者將為顯而易見的且欲包括於本發明之真正範疇內且可在不脫離本發明之真正範疇的情況下進行。
實例 實例 1 構築貓 IgG Fc 突變體
如Strietzel等人(Strietzel等人, 2014,
Vet Immunol Immunopathol., 第158(3-4)卷, 第214至223頁)所描述,實施所有貓IgG之構築(
圖 1),其中利用含有編碼IgG子類1對偶基因a (IgG1a)之貓恆定區之序列的質體,且本文所研究之各mAb之VH/VL序列經插入上游且與編碼恆定域之核苷酸同框。使用Agilent's QuikChange II突變誘發及用於單點定向突變誘發的相關Agilent引子設計工具將突變併入至各質體之CH3域(圖2)之位置S434及S428中(https://www.agilent.com/store/primerDesignProgram.jsp)。
抗體構築體使用標準脂染胺轉染方案(Invitrogen Life Technologies,Carlsbad,CA,USA)在HEK 293細胞中暫時表現或使用ExpiCHO瞬時系統(ThermoFisher Scientific)套組方案在CHO細胞中暫時表現。ExpiCHO表現遵循由ThermoFisher概述之方案,以共轉染含有編碼IgG輕鏈及IgG重鏈之基因序列的質體。針對HEK293表現,共轉染按重量計之等量重鏈質體及輕鏈質體。使細胞生長7天,之後採集上清液用於抗體純化。經由Octet QKe定量(Pall ForteBio Corp, Menlo Park, CA, USA)篩檢結合於蛋白質A感測器之抗體。針對蛋白質品質,如Strietzel等人中所描述來純化且定量結合於蛋白質A之構築體。
實例 2 目標結合親和力及效能分析
藉由Biacore評估各mAb之親和力且經由適合的基於細胞之效能分析來測定IC50。在Biacore T200 (GE Healthcare, Pittsburgh, PA)上進行表面電漿子共振以量測各抗體針對其目標之結合親和力,2.5 μg/ml之各目標蛋白質藉由使用最終密度約250個RU (共振單位)之EDC/NHS分別在CM5感測器流通池2至4上進行胺偶合來固定。
流通池1用作內部參考以校正操作緩衝液效應。在15℃下以250 s之接觸時間及30 μl/min之流速量測抗體結合。解離時段為300 s。每一者用再生緩衝液(10 mM甘胺酸pH1.5及10 mM NaOH)及20 μl/min之流速進行再生60 s。在相同的分析形式下,操作/稀釋緩衝液(1×HBS-EP、GE Healthcare,BR-1006-69,10×包括100 mM HEPES、150 mM NaCl、30 mM EDTA及0.5% v/v界面活性劑P20、pH7.4,1:10於過濾MQ H2O中)用作陰性對照。
藉由使用雙重參照之方法用Biacore T200評估軟體來分析資料。所得曲線與1:1結合模型擬合。在野生型以及S434及S428突變IgG之間未觀測到結合親和力或IC50之差異(
表 1)。
表 1.WT以及S434及S428突變IgG之親和力及效力。在WT與突變IgG之間未量測到差異:
ND係指未測定。
mAb1係指貓類化抗IL31抗體。抗IL31抗體為此項技術中所熟知的。參見例如,美國專利10,526,405;10,421,807;9,206,253;8,790,651。mAb2及mAb3係指貓類化抗NGF抗體。抗NGF抗體亦為此項技術中所熟知的。參見例如,美國專利10,125,192;10,093,725;9,951,128;9,617,334;及9,505,829。mAb6係指貓類化抗TGFβ抗體。抗TGFβ抗體亦為此項技術中眾所周知的。參見例如美國專利申請案63/036,092及63/248,679。
實例 3 活體外 FcRn 結合分析
分離、製備貓FcRn,且根據Strietzelg等人分析針對貓FcRn之突變Fc IgG。使用標準RACE PCR來擴增貓FcRn-α次單元及β-微球蛋白。FcRn-α次單元及β-微球蛋白經共轉染至HEK 293細胞中且FcRn複合體係藉由經由c端His標籤進行IMAC親和純化來純化。藉由Biacore 3000或Biacore T200 (GE Healthcare,Pittsburgh, PA, USA)使用CM5感測器晶片量測KD。
使用標準胺固定方法將FcRn固定在感測器表面上以達至所需表面密度。HBS-EP用作固定操作緩衝液,且將10mM MES;150mM NaCl;0.005% Tween20;0.5 mg/mL BSA;pH6及pH7.2及PBS;0.005% Tween20;0.5 mg/mL BSA;pH7.4用於方法操作緩衝液及滴定。Fc突變IgG在受體表面上流動且使用Scrubber2軟體分析(BioLogic Software Pty, Ltd., Campbell, Australia)或T200評估軟體測定親和力(
表 2)。自所有操作中減去僅含有緩衝液之空白操作。流通池使用50 mM Tris pH8進行再生。在15℃下進行操作。
在位置434及428產生的突變對於pH6下IgG針對FcRn之親和力具有明顯影響。此研究顯示IgG之FcRn親和力增加並非取決於VHVL域,且對於任何貓IgG1a而言係通用的。
表 2.藉由表面電漿子共振(Biacore)量測的野生型(WT)、N434及S428突變IgG與貓FcRn之結合:
NBO係指未觀測到結合。
mAb1係指貓類化抗IL31抗體,如表1中所論述。mAb2及mAb3係指貓類化抗NGF抗體,如表1中所論述。mAb6係指貓類化抗TGFβ抗體,如表1中所論述。
表 3.藉由表面電漿子共振(Biacore)量測的野生型(WT)及N434突變IgG與貓FcRn之結合:
使用抗NGF抗體。
實例 4 貓之 Fc 突變 IgG PK 研究
實施藥物動力學(PK)研究以顯示針對多種目標,半衰期延長突變S434H及S428L對於具有mAb之IgG1a子類之影響提高。研究設計多種多樣,但基本上實施兩種類型之研究:
研究設計1:mAb係以每劑2 mg/kg向4隻雄性及4隻雌性短毛家貓之群組投與。間隔28天皮下投與第一劑量與第二劑量。28天後靜脈內投與第三劑量。每週收集血清樣品一次持續14週。
研究設計2:mAb係以2 mg/kg之單劑量形式向3或4隻短毛家貓之群組皮下或靜脈內投與。每週收集血清樣品一次。
使用藉助於Watson™之非隔室途徑(用於AUC計算之直線梯形法則)來進行藥物動力學計算。藉由Excel™進行其他計算,包括校正第2次及第3次注射藥物之後的濃度-時間特徵曲線之重疊的AUC。使用Excel™或Watson™計算濃度-時間資料及藥物動力學資料在簡單統計下之彙總(均值、標準差、變化係數)。未實施其他統計分析。
表 4.野生型以及S428L及S434H突變貓IgG之計算半衰期:
mAb1係指貓類化抗IL31抗體。抗IL31抗體為此項技術中所熟知的。參見例如,美國專利10,526,405;10,421,807;9,206,253;8,790,651。mAb2及mAb3係指貓類化抗NGF抗體。抗NGF抗體亦為此項技術中所熟知的。參見例如,美國專利10,125,192;10,093,725;9,951,128;9,617,334;及9,505,829。mAb6係指貓類化抗TGFβ抗體。抗TGFβ抗體亦為此項技術中眾所周知的。參見例如美國專利申請案63/036,092及63/248,679。
貓IgG1a點突變S428L已顯示短毛家貓中之三種不同貓IgG之半衰期延長了2.5至3倍。對於mAb1,半衰期自11天延長至26天,且對於mAb2,半衰期自7.9天延長至23天,且對於mAb4,半衰期自5.9天延長至15.5天。貓IgG1a點突變S434H已顯示一種mAb之半衰期自10.1天延長至13.2天。
作用機制係經由增強在pH6下針對貓FcRn之親和力,且已證實多種貓IgG結合了極不同且獨特的可溶性目標。因此,證實貓IgG1a之S428L及N434突變之半衰期延長與VHVL域無關。
實例 5 FcRn 結合分析
分離、製備貓FcRn,且根據上文所論述之Strietzel等人分析針對貓FcRn之突變Fc IgG。使用標準PCR來擴增貓FcRn-α次單元及β-微球蛋白。FcRn-α次單元及β-微球蛋白經共轉染至HEK 293細胞中且FcRn複合體係藉由經由c端His標籤進行IMAC親和純化來純化。FcRn複合體經由BirA酶促生物素醯化反應來進行生物素標記。藉由Biacore T200 (GE Healthcare,Pittsburgh, PA, USA)或Biacore 8K (Cytiva, Marlborough, MA, USA)使用SA感測器晶片量測KD。
使用修改之SA捕獲方法將FcRn捕獲於感測器表面上。10mM MES;150mM NaCl;0.005% Tween20;0.5 mg/mL BSA;pH6用作捕獲方法操作緩衝液及滴定。1×HB-P、0.5 mg/mL BSA;pH7.4亦用於方法操作緩衝液及滴定。Fc突變IgG在受體表面上流動,且使用T200評估軟體或Biacore Insight評估軟體測定親和力。自所有操作中減去僅含有緩衝液之空白操作。流通池使用50 mM Tris pH8或pH9進行再生。在15℃下進行操作。
在各別位置產生的突變對於pH6下IgG針對FcRn之親和力具有明顯影響。藉由表面電漿子共振(Biacore)量測野生型(WT)及突變IgG與貓FcRn之結合。
在結合不同目標之完全不同且結構上不同的抗體(亦即,抗IL31及抗NGF抗體)以及結合相同目標之不同版本抗體(亦即,不同版本之抗IL31及抗NGF抗體)中觀測到對於親和力之明顯影響(表1至表5)。因此,針對IgG之FcRn親和力增加並不取決於VHVL域或CDR區。另外,在多種IgG子類中觀測到對於親和力之明顯影響。大體而言,結果顯示針對IgG之FcRn親和力增加與貓IgG子類無關。
表 5A.野生型(WT)及S428及S434突變IgG與貓FcRn之結合
mAb4及mAb3分別係指貓類化抗IL31 (ZTS-5864)及抗NGF (ZTS-768)抗體。此表及以上表1、2及4中之mAb3為相同的(亦即,ZTS-768)。然而,相對於表1、2及4中列舉之mAb2抗體,此表中之mAb3具有不同的VL、VH及CDR區。
NBO=未觀測到結合。
表 5B.野生型(WT)及S428及S434突變IgG與貓FcRn之結合
mAb4及mAb5係指貓類化抗IL31抗體。相對於mAb5,mAb4具有不同的VL、VH及CDR區。
NBO=未觀測到結合。
實例 6 FcRn 結合分析
如以上實例部分中所論述,分離、製備貓FcRn且根據Strietzelg等人分析針對貓FcRn之突變Fc IgG。使用標準RACE PCR來擴增貓FcRn-α次單元及β-微球蛋白。FcRn-α次單元及β-微球蛋白經共轉染至HEK 293細胞中且FcRn複合體係藉由經由c端His標籤進行IMAC親和純化來純化。藉由Biacore 3000或Biacore T200 (GE Healthcare,Pittsburgh, PA, USA)使用CM5感測器晶片量測KD。
使用修改之SA捕獲方法將FcRn捕獲於感測器表面上。10mM MES;150mM NaCl;0.005% Tween20;0.5 mg/mL BSA;pH6用作捕獲方法操作緩衝液及滴定。1×HB-P、0.5 mg/mL BSA;pH7.4亦用於方法操作緩衝液及滴定。Fc突變IgG在受體表面上流動,且使用T200評估軟體或Biacore Insight評估軟體測定親和力。自所有操作中減去僅含有緩衝液之空白操作。流通池使用50 mM Tris pH8或pH9進行再生。在15℃下進行操作。
在位置434及428產生的突變對於pH6下IgG針對FcRn之親和力具有明顯影響。此研究揭示針對IgG之FcRn親和力增加並不取決於VHVL域。
表 6a.藉由表面電漿子共振(Biacore)量測的野生型(WT)及N434突變IgG與貓FcRn之結合:
使用貓IgG1a子類B。
NBO =未觀測到結合;WT及S434H突變型之核酸密碼子分別為AGC及CAC。
ID編號1、12、14、16、及18分別表示野生型mAb6抗TGFβ抗體ZTS-310、ZTS-120-1、ZTS-120-2、ZTS-120-3及ZTS-120-4。ID編號2、13、15、17及19分別表示突變型mAb6抗TGFβ抗體ZTS-310、ZTS-120-1、ZTS-120-2、ZTS-120-3及ZTS-120-4。
表 6b.藉由表面電漿子共振(Biacore)量測的野生型(WT)及N434突變IgG與貓FcRn之結合:
使用貓IgG1a子類B。
NBO=未觀測到結合;WT及S434H突變型之核酸密碼子分別為AGC及CAC。
ID編號20、22、24、26及28分別表示野生型mAb6抗TGFβ抗體ZTS-120-5、ZTS-120-6、ZTS-120-7、ZTS-120-8及ZTS-120-9。ID編號21、23、25、27及29分別表示突變型mAb6抗TGFβ抗體ZTS-120-5、ZTS-120-6、ZTS-120-7、ZTS-120-8及ZTS-120-9。
表 6c.藉由表面電漿子共振(Biacore)量測的野生型(WT)及N434突變IgG與貓FcRn之結合:
使用貓IgG1a子類B。
NBO=未觀測到結合。
ID編號1表示野生型抗TGFβ抗體ZTS-310。
ID編號2至11表示抗TGFβ抗體ZTS-310之突變形式。
已描述本發明之較佳實施例,應理解,本發明不限於確切實施例,且各種變化及修改可由熟習此項技術者在不偏離本發明之如所附申請專利範圍中定義的範疇或精神之情況下於其中實現。
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[圖1]展示IgG之域結構。在CH3域中產生Fc突變S428L及/或N434H以藉由延長pH6下之針對FcRn之親和力來延長IgG半衰期。
[圖2A]展示野生型(WT)人類IgG1、WT貓IgG1a、WT貓IgG1b、WT貓IgG2及具有鉸鏈突變之突變貓IgG2的胺基酸序列之比對。胺基酸殘基係根據如Kabat中之EU索引進行編號。CH1、鉸鏈、CH2及CH3胺基酸殘基分別呈紅色、紫色、藍色及綠色。[圖2B]展示貓Fc IgG1a WT核苷酸序列。[圖2C]展示貓Fc IgG1a S434H核苷酸序列。[圖2D]展示貓Fc IgG1a S428L核苷酸序列。
[圖3]展示在98天時間段內量測的8隻貓(4至雄性(G00397、G00398、G00399、G00400)及4隻雌性(G00425、G00426、G00427、G00428))在三次注射2mg/kg (SC/SC/IV)之後,其體內之WT mAb1 IgG的各別血清濃度。
[圖4]展示在98天時間段內量測的8隻貓(4至雄性(G00417、G00418、G00419、G00420)及4隻雌性(G00445、G00446、G00447、G0448))在三次注射2mg/kg (SC/SC/IV)之後,其體內之WT mAb1 IgG的各別血清濃度。
[圖5]展示在30天時間段內量測的3隻貓在次皮下注射2mg/kg之後,其體內之WT mAb2的各別血清濃度。
[圖6]展示在30天時間段內量測的3隻貓在單次皮下注射2mg/kg之後,其體內之突變S428L mAb2的各別血清濃度。
[圖7]展示在21天時間段內量測的貓在單次皮下注射2mg/kg之後,其體內之突變S428L mAb3的各別血清濃度。
[圖8]展示在98天時間段內量測的8隻貓(4隻雄性(G00453、G00454、G00455、G00456)及4隻雌性(G00457、G00458、G00459、G00460))在三次注射2mg/kg (SC/SC/IV)之後,其體內之WT mAb3 IgG的各別血清濃度。
[圖9]展示在98天時間段內量測的8隻貓(4隻雄性(G00469、G00470、G00471、G00472)及4隻雌性(G00473、G00474、G00475、G0476))在三次注射2mg/kg (SC/SC/IV)之後,其體內之S434H mAb3 IgG的各別血清濃度。
序列表的簡要說明
SEQ ID NO.:1為具有S428L突變之突變IgG1a恆定域之胺基酸序列。
SEQ ID NO.:2為具有S434H突變之突變IgG1a恆定域之胺基酸序列。
SEQ ID NO.:3為野生型IgG1a恆定域之胺基酸序列。
SEQ ID NO.:4為野生型IgG1a恆定域之核酸序列。
SEQ ID NO.:5為IgG1a CH1域之胺基酸序列。
SEQ ID NO.:6為IgG1a鉸鏈域之胺基酸序列。
SEQ ID NO.:7為IgG1a CH2域之胺基酸序列。
SEQ ID NO.:8為IgG1a WTCH3域之胺基酸序列。
SEQ ID NO.:9為IgG1a CH1域之核酸序列。
SEQ ID NO.:10為IgG1a鉸鏈域之核酸序列。
SEQ ID NO.:11為IgG1a CH2域之核酸序列。
SEQ ID NO.:12為IgG1a WTCH3域之核酸序列。
SEQ ID NO.:13為抗IL31抗體(ZTS-5864)重鏈可變區之核酸序列。
SEQ ID NO.:14為抗IL31抗體(ZTS-5864)重鏈可變區之胺基酸序列。
SEQ ID NO.:15為抗IL31抗體(ZTS-5864)重鏈可變區CDR1之胺基酸序列。
SEQ ID NO.:16為抗IL31抗體(ZTS-5864)重鏈可變區CDR2之胺基酸序列。
SEQ ID NO.:17為抗IL31抗體(ZTS-5864)重鏈可變區CDR3之胺基酸序列。
SEQ ID NO.:18為抗IL31抗體(ZTS-5864)輕鏈可變區之核酸序列。
SEQ ID NO.:19為抗IL31抗體(ZTS-5864)輕鏈可變區之胺基酸序列。
SEQ ID NO.:20為抗IL31抗體(ZTS-5864)輕鏈可變區CDR1之胺基酸序列。
SEQ ID NO.:21為抗IL31抗體(ZTS-5864)輕鏈可變區CDR2之胺基酸序列。
SEQ ID NO.:22為抗IL31抗體(ZTS-5864)輕鏈可變區CDR3之胺基酸序列。
SEQ ID NO.:23為抗NGF抗體(ZTS768)重鏈之胺基酸序列。
SEQ ID NO.:24為抗NGF抗體(ZTS768)重鏈CDR1之胺基酸序列。
SEQ ID NO.:25為抗NGF抗體(ZTS768)重鏈CDR2之胺基酸序列。
SEQ ID NO.:26為抗NGF抗體(ZTS768)重鏈CDR3之胺基酸序列。
SEQ ID NO.:27為抗NGF抗體(ZTS768)輕鏈之胺基酸序列。
SEQ ID NO.:28為抗NGF抗體(ZTS768)輕鏈CDR1之胺基酸序列。
SEQ ID NO.:29為抗NGF抗體(ZTS768)輕鏈CDR2之胺基酸序列。
SEQ ID NO.:30為抗NGF抗體(ZTS768)輕鏈CDR3之胺基酸序列。
SEQ ID NO.:31為抗NGF抗體(NV02)重鏈之胺基酸序列。
SEQ ID NO.:32為抗NGF抗體(NV02)重鏈CDR1之胺基酸序列。
SEQ ID NO.:33為抗NGF抗體(NV02)重鏈CDR2之胺基酸序列。
SEQ ID NO.:34為抗NGF抗體(NV02)重鏈CDR3之胺基酸序列。
SEQ ID NO.:35為抗NGF抗體(NV02) κ鏈之胺基酸序列。
SEQ ID NO.:36為抗NGF抗體(NV02) κ鏈CDR1之胺基酸序列。
SEQ ID NO.:37為抗NGF抗體(NV02) κ鏈CDR2之胺基酸序列。
SEQ ID NO.:38為抗NGF抗體(NV02) κ鏈CDR3之胺基酸序列。
SEQ ID NO:39為本文中稱為ZTS-310之抗TGFβ1,3抗體之可變重鏈CDR1;
SEQ ID NO:40為本文中稱為ZTS-310之抗TGFβ1,3抗體之可變重鏈CDR2;
SEQ ID NO:41為本文中稱為ZTS-310之抗TGFβ1,3抗體之可變重鏈CDR3;
SEQ ID NO:42為本文中稱為ZTS-310之抗TGFβ1,3抗體之可變輕鏈CDR1;
SEQ ID NO:43為本文中稱為ZTS-310之抗TGFβ1,3抗體之可變輕鏈CDR2;
SEQ ID NO:44為本文中稱為ZTS-310之抗TGFβ1,3抗體之可變輕鏈CDR3;
SEQ ID NO:45為本文中稱為ZTS-310之抗TGFβ1,3抗體之重鏈的胺基酸序列;
SEQ ID NO:46為本文中稱為ZTS-310之抗TGFβ1,3抗體之重鏈的核酸序列。
SEQ ID NO:47為本文中稱為ZTS-310之抗TGFβ1,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:48為本文中稱為ZTS-310之抗TGFβ1,3抗體之輕鏈的核酸序列;
SEQ ID NO:49為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:50為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:51為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:52為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:53為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:54為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:55為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:56為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:57為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:58為本文中稱為ZTS-120-1之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
SEQ ID NO:59為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:60為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:61為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:62為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:63為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:64為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:65為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:66為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:67為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:68為本文中稱為ZTS-120-2之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
SEQ ID NO:69為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:70為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:71為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:72為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:73為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:74為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:75為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:76為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:77為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:78為本文中稱為ZTS-120-3之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
SEQ ID NO:79為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:80為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:81為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:82為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:83為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:84為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:85為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:86為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:87為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:88為本文中稱為ZTS-120-4之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
SEQ ID NO:89為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:90為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:91為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:92為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:93為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:94為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:95為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:96為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:97為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:98為本文中稱為ZTS-120-5之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
SEQ ID NO:99為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:100為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:101為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:102為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:103為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:104為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:105為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:106為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:107為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:108為本文中稱為ZTS-120-6之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
SEQ ID NO:109為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:110為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:111為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:112為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:113為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:114為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:115為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:116為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:117為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:118為本文中稱為ZTS-120-7之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
SEQ ID NO:119為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:120為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:121為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:122為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:123為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:124為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:125為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:126為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:127為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:128為本文中稱為ZTS-120-8之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
SEQ ID NO:129為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之可變重鏈CDR1;
SEQ ID NO:130為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之可變重鏈CDR2;
SEQ ID NO:131為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之可變重鏈CDR3;
SEQ ID NO:132為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之可變輕鏈CDR1;
SEQ ID NO:133為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之可變輕鏈CDR2;
SEQ ID NO:134為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之可變輕鏈CDR3;
SEQ ID NO:135為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之重鏈的胺基酸序列;
SEQ ID NO:136為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之重鏈的核酸序列;
SEQ ID NO:137為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之輕鏈的胺基酸序列;
SEQ ID NO:138為本文中稱為ZTS-120-9之抗TGFβ1,2,3抗體之輕鏈的核酸序列;
<![CDATA[<110> 碩騰服務公司(Zoetis Services LLC)]]> <![CDATA[<120> 貓抗體變異體]]> <![CDATA[<140> TW 110136252]]> <![CDATA[<141> 2021-09-29]]> <![CDATA[<150> US 63/084,693]]> <![CDATA[<151> 2020-09-29]]> <![CDATA[<160> 138 ]]> <![CDATA[<170> PatentIn 版本 3.5]]> <![CDATA[<210> 1]]> <![CDATA[<211> 335]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 1]]> Ala Ser Thr Thr Ala Pro Ser Val Phe Pro Leu Ala Pro Ser Cys Gly 1 5 10 15 Thr Thr Ser Gly Ala Thr Val Ala Leu Ala Cys Leu Val Leu Gly Tyr 20 25 30 Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser 35 40 45 Gly Val His Thr Phe Pro Ala Val Leu Gln Ala Ser Gly Leu Tyr Ser 50 55 60 Leu Ser Ser Met Val Thr Val Pro Ser Ser Arg Trp Leu Ser Asp Thr 65 70 75 80 Phe Thr Cys Asn Val Ala His Pro Pro Ser Asn Thr Lys Val Asp Lys 85 90 95 Thr Val Arg Lys Thr Asp His Pro Pro Gly Pro Lys Pro Cys Asp Cys 100 105 110 Pro Lys Cys Pro Pro Pro Glu Met Leu Gly Gly Pro Ser Ile Phe Ile 115 120 125 Phe Pro Pro Lys Pro Lys Asp Thr Leu Ser Ile Ser Arg Thr Pro Glu 130 135 140 Val Thr Cys Leu Val Val Asp Leu Gly Pro Asp Asp Ser Asp Val Gln 145 150 155 160 Ile Thr Trp Phe Val Asp Asn Thr Gln Val Tyr Thr Ala Lys Thr Ser 165 170 175 Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser Val Leu 180 185 190 Pro Ile Leu His Gln Asp Trp Leu Lys Gly Lys Glu Phe Lys Cys Lys 195 200 205 Val Asn Ser Lys Ser Leu Pro Ser Pro Ile Glu Arg Thr Ile Ser Lys 210 215 220 Ala Lys Gly Gln Pro His Glu Pro Gln Val Tyr Val Leu Pro Pro Ala 225 230 235 240 Gln Glu Glu Leu Ser Arg Asn Lys Val Ser Val Thr Cys Leu Ile Lys 245 250 255 Ser Phe His Pro Pro Asp Ile Ala Val Glu Trp Glu Ile Thr Gly Gln 260 265 270 Pro Glu Pro Glu Asn Asn Tyr Arg Thr Thr Pro Pro Gln Leu Asp Ser 275 280 285 Asp Gly Thr Tyr Phe Val Tyr Ser Lys Leu Ser Val Asp Arg Ser His 290 295 300 Trp Gln Arg Gly Asn Thr Tyr Thr Cys Ser Val Leu His Glu Ala Leu 305 310 315 320 His Ser His His Thr Gln Lys Ser Leu Thr Gln Ser Pro Gly Lys 325 330 335 <![CDATA[<210> 2]]> <![CDATA[<211> 335]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 2]]> Ala Ser Thr Thr Ala Pro Ser Val Phe Pro Leu Ala Pro Ser Cys Gly 1 5 10 15 Thr Thr Ser Gly Ala Thr Val Ala Leu Ala Cys Leu Val Leu Gly Tyr 20 25 30 Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser 35 40 45 Gly Val His Thr Phe Pro Ala Val Leu Gln Ala Ser Gly Leu Tyr Ser 50 55 60 Leu Ser Ser Met Val Thr Val Pro Ser Ser Arg Trp Leu Ser Asp Thr 65 70 75 80 Phe Thr Cys Asn Val Ala His Pro Pro Ser Asn Thr Lys Val Asp Lys 85 90 95 Thr Val Arg Lys Thr Asp His Pro Pro Gly Pro Lys Pro Cys Asp Cys 100 105 110 Pro Lys Cys Pro Pro Pro Glu Met Leu Gly Gly Pro Ser Ile Phe Ile 115 120 125 Phe Pro Pro Lys Pro Lys Asp Thr Leu Ser Ile Ser Arg Thr Pro Glu 130 135 140 Val Thr Cys Leu Val Val Asp Leu Gly Pro Asp Asp Ser Asp Val Gln 145 150 155 160 Ile Thr Trp Phe Val Asp Asn Thr Gln Val Tyr Thr Ala Lys Thr Ser 165 170 175 Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser Val Leu 180 185 190 Pro Ile Leu His Gln Asp Trp Leu Lys Gly Lys Glu Phe Lys Cys Lys 195 200 205 Val Asn Ser Lys Ser Leu Pro Ser Pro Ile Glu Arg Thr Ile Ser Lys 210 215 220 Ala Lys Gly Gln Pro His Glu Pro Gln Val Tyr Val Leu Pro Pro Ala 225 230 235 240 Gln Glu Glu Leu Ser Arg Asn Lys Val Ser Val Thr Cys Leu Ile Lys 245 250 255 Ser Phe His Pro Pro Asp Ile Ala Val Glu Trp Glu Ile Thr Gly Gln 260 265 270 Pro Glu Pro Glu Asn Asn Tyr Arg Thr Thr Pro Pro Gln Leu Asp Ser 275 280 285 Asp Gly Thr Tyr Phe Val Tyr Ser Lys Leu Ser Val Asp Arg Ser His 290 295 300 Trp Gln Arg Gly Asn Thr Tyr Thr Cys Ser Val Ser His Glu Ala Leu 305 310 315 320 His His His His Thr Gln Lys Ser Leu Thr Gln Ser Pro Gly Lys 325 330 335 <![CDATA[<210> 3]]> <![CDATA[<211> 335]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 3]]> Ala Ser Thr Thr Ala Pro Ser Val Phe Pro Leu Ala Pro Ser Cys Gly 1 5 10 15 Thr Thr Ser Gly Ala Thr Val Ala Leu Ala Cys Leu Val Leu Gly Tyr 20 25 30 Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser 35 40 45 Gly Val His Thr Phe Pro Ala Val Leu Gln Ala Ser Gly Leu Tyr Ser 50 55 60 Leu Ser Ser Met Val Thr Val Pro Ser Ser Arg Trp Leu Ser Asp Thr 65 70 75 80 Phe Thr Cys Asn Val Ala His Pro Pro Ser Asn Thr Lys Val Asp Lys 85 90 95 Thr Val Arg Lys Thr Asp His Pro Pro Gly Pro Lys Pro Cys Asp Cys 100 105 110 Pro Lys Cys Pro Pro Pro Glu Met Leu Gly Gly Pro Ser Ile Phe Ile 115 120 125 Phe Pro Pro Lys Pro Lys Asp Thr Leu Ser Ile Ser Arg Thr Pro Glu 130 135 140 Val Thr Cys Leu Val Val Asp Leu Gly Pro Asp Asp Ser Asp Val Gln 145 150 155 160 Ile Thr Trp Phe Val Asp Asn Thr Gln Val Tyr Thr Ala Lys Thr Ser 165 170 175 Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser Val Leu 180 185 190 Pro Ile Leu His Gln Asp Trp Leu Lys Gly Lys Glu Phe Lys Cys Lys 195 200 205 Val Asn Ser Lys Ser Leu Pro Ser Pro Ile Glu Arg Thr Ile Ser Lys 210 215 220 Ala Lys Gly Gln Pro His Glu Pro Gln Val Tyr Val Leu Pro Pro Ala 225 230 235 240 Gln Glu Glu Leu Ser Arg Asn Lys Val Ser Val Thr Cys Leu Ile Lys 245 250 255 Ser Phe His Pro Pro Asp Ile Ala Val Glu Trp Glu Ile Thr Gly Gln 260 265 270 Pro Glu Pro Glu Asn Asn Tyr Arg Thr Thr Pro Pro Gln Leu Asp Ser 275 280 285 Asp Gly Thr Tyr Phe Val Tyr Ser Lys Leu Ser Val Asp Arg Ser His 290 295 300 Trp Gln Arg Gly Asn Thr Tyr Thr Cys Ser Val Ser His Glu Ala Leu 305 310 315 320 His Ser His His Thr Gln Lys Ser Leu Thr Gln Ser Pro Gly Lys 325 330 335 <![CDATA[<210> 4]]> <![CDATA[<211> 1005]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 4]]> gcctccacca cggccccatc ggtgttccca ctggccccca gctgcgggac cacatctggc 60 gccaccgtgg ccctggcctg cctggtgtta ggctacttcc ctgagccggt gaccgtgtcc 120 tggaactccg gcgccctgac cagcggtgtg cacaccttcc cggccgtcct gcaggcctcg 180 gggctgtact ctctcagcag catggtgaca gtgccctcca gcaggtggct cagtgacacc 240 ttcacctgca acgtggccca cccgcccagc aacaccaagg tggacaagac cgtgcgcaaa 300 acagaccacc caccgggacc caaaccctgc gactgtccca aatgcccacc ccctgagatg 360 cttggaggac cgtccatctt catcttcccc ccaaaaccca aggacaccct ctcgatttcc 420 cggacgcccg aggtcacatg cttggtggtg gacttgggcc cagatgactc cgatgtccag 480 atcacatggt ttgtggataa cacccaggtg tacacagcca agacgagtcc gcgtgaggag 540 cagttcaaca gcacctaccg tgtggtcagt gtcctcccca tcctacacca ggactggctc 600 aaggggaagg agttcaagtg caaggtcaac agcaaatccc tcccctcccc catcgagagg 660 accatctcca aggccaaagg acagccccac gagccccagg tgtacgtcct gcctccagcc 720 caggaggagc tcagcaggaa caaagtcagt gtgacctgcc tgatcaaatc cttccacccg 780 cctgacattg ccgtcgagtg ggagatcacc ggacagccgg agccagagaa caactaccgg 840 acgaccccgc cccagctgga cagcgacggg acctacttcg tgtacagcaa gctctcggtg 900 gacaggtccc actggcagag gggaaacacc tacacctgct cggtgtcaca cgaagctctg 960 cacagccacc acacacagaa atccctcacc cagtctccgg gtaaa 1005 <![CDATA[<210> 5]]> <![CDATA[<211> 98]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 5]]> Ala Ser Thr Thr Ala Pro Ser Val Phe Pro Leu Ala Pro Ser Cys Gly 1 5 10 15 Thr Thr Ser Gly Ala Thr Val Ala Leu Ala Cys Leu Val Leu Gly Tyr 20 25 30 Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser 35 40 45 Gly Val His Thr Phe Pro Ala Val Leu Gln Ala Ser Gly Leu Tyr Ser 50 55 60 Leu Ser Ser Met Val Thr Val Pro Ser Ser Arg Trp Leu Ser Asp Thr 65 70 75 80 Phe Thr Cys Asn Val Ala His Pro Pro Ser Asn Thr Lys Val Asp Lys 85 90 95 Thr Val <![CDATA[<210> 6]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 6]]> Arg Lys Thr Asp His Pro Pro Gly Pro Lys Pro Cys Asp Cys Pro Lys 1 5 10 15 Cys Pro <![CDATA[<210> 7]]> <![CDATA[<211> 110]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 7]]> Pro Pro Glu Met Leu Gly Gly Pro Ser Ile Phe Ile Phe Pro Pro Lys 1 5 10 15 Pro Lys Asp Thr Leu Ser Ile Ser Arg Thr Pro Glu Val Thr Cys Leu 20 25 30 Val Val Asp Leu Gly Pro Asp Asp Ser Asp Val Gln Ile Thr Trp Phe 35 40 45 Val Asp Asn Thr Gln Val Tyr Thr Ala Lys Thr Ser Pro Arg Glu Glu 50 55 60 Gln Phe Asn Ser Thr Tyr Arg Val Val Ser Val Leu Pro Ile Leu His 65 70 75 80 Gln Asp Trp Leu Lys Gly Lys Glu Phe Lys Cys Lys Val Asn Ser Lys 85 90 95 Ser Leu Pro Ser Pro Ile Glu Arg Thr Ile Ser Lys Ala Lys 100 105 110 <![CDATA[<210> 8]]> <![CDATA[<211> 109]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 8]]> Gly Gln Pro His Glu Pro Gln Val Tyr Val Leu Pro Pro Ala Gln Glu 1 5 10 15 Glu Leu Ser Arg Asn Lys Val Ser Val Thr Cys Leu Ile Lys Ser Phe 20 25 30 His Pro Pro Asp Ile Ala Val Glu Trp Glu Ile Thr Gly Gln Pro Glu 35 40 45 Pro Glu Asn Asn Tyr Arg Thr Thr Pro Pro Gln Leu Asp Ser Asp Gly 50 55 60 Thr Tyr Phe Val Tyr Ser Lys Leu Ser Val Asp Arg Ser His Trp Gln 65 70 75 80 Arg Gly Asn Thr Tyr Thr Cys Ser Val Ser His Glu Ala Leu His Ser 85 90 95 His His Thr Gln Lys Ser Leu Thr Gln Ser Pro Gly Lys 100 105 <![CDATA[<210> 9]]> <![CDATA[<211> 294]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 9]]> gcctccacca cggccccatc ggtgttccca ctggccccca gctgcgggac cacatctggc 60 gccaccgtgg ccctggcctg cctggtgtta ggctacttcc ctgagccggt gaccgtgtcc 120 tggaactccg gcgccctgac cagcggtgtg cacaccttcc cggccgtcct gcaggcctcg 180 gggctgtact ctctcagcag catggtgaca gtgccctcca gcaggtggct cagtgacacc 240 ttcacctgca acgtggccca cccgcccagc aacaccaagg tggacaagac cgtg 294 <![CDATA[<210> 10]]> <![CDATA[<211> 54]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 10]]> cgcaaaacag accacccacc gggacccaaa ccctgcgact gtcccaaatg ccca 54 <![CDATA[<210> 11]]> <![CDATA[<211> 330]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 11]]> ccccctgaga tgcttggagg accgtccatc ttcatcttcc ccccaaaacc caaggacacc 60 ctctcgattt cccggacgcc cgaggtcaca tgcttggtgg tggacttggg cccagatgac 120 tccgatgtcc agatcacatg gtttgtggat aacacccagg tgtacacagc caagacgagt 180 ccgcgtgagg agcagttcaa cagcacctac cgtgtggtca gtgtcctccc catcctacac 240 caggactggc tcaaggggaa ggagttcaag tgcaaggtca acagcaaatc cctcccctcc 300 cccatcgaga ggaccatctc caaggccaaa 330 <![CDATA[<210> 12]]> <![CDATA[<211> 327]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 家貓(Felis catus)]]> <![CDATA[<400> 12]]> ggacagcccc acgagcccca ggtgtacgtc ctgcctccag cccaggagga gctcagcagg 60 aacaaagtca gtgtgacctg cctgatcaaa tccttccacc cgcctgacat tgccgtcgag 120 tgggagatca ccggacagcc ggagccagag aacaactacc ggacgacccc gccccagctg 180 gacagcgacg ggacctactt cgtgtacagc aagctctcgg tggacaggtc ccactggcag 240 aggggaaaca cctacacctg ctcggtgtca cacgaagctc tgcacagcca ccacacacag 300 aaatccctca cccagtctcc gggtaaa 327 <![CDATA[<210> 13]]> <![CDATA[<211> 351]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> ZTS-5864重鏈可變區]]> <![CDATA[<400> 13]]> gacgtgcaat tggtggagtc tgggggagac ctggtgaagc ctggggggtc cctgagactc 60 acctgtgtgg cctctggatt caccttcagt gactatgcaa tgagctgggt ccgccaggct 120 ccagggaagg ggctgcagtg ggtcgcaggt attgacagtg ttggaagtgg cacaagctac 180 gcagactccg tgaagggccg attcaccatc tccagagaca atgccaagaa cacgctgtat 240 ctgcagatga acagcctcaa gaccgaggac acggccacat attactgtgc gagcgggttc 300 cctgggtcct ttgagcactg gggccaagga accctggtga cggtctcgag c 351 <![CDATA[<210> 14]]> <![CDATA[<211> 117]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> ZTS-5864重鏈可變區]]> <![CDATA[<400> 14]]> Asp Val Gln Leu Val Glu Ser Gly Gly Asp Leu Val Lys Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Thr Cys Val Ala Ser Gly Phe Thr Phe Ser Asp Tyr 20 25 30 Ala Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Gln Trp Val 35 40 45 Ala Gly Ile Asp Ser Val Gly Ser Gly Thr Ser Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Thr Glu Asp Thr Ala Thr Tyr Tyr Cys 85 90 95 Ala Ser Gly Phe Pro Gly Ser Phe Glu His Trp Gly Gln Gly Thr Leu 100 105 110 Val Thr Val Ser Ser 115 <![CDATA[<210> 15]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家犬(Canis familiaris)]]> <![CDATA[<400> 15]]> Asp Tyr Ala Met Ser 1 5 <![CDATA[<210> 16]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家犬(Canis familiaris)]]> <![CDATA[<400> 16]]> Gly Ile Asp Ser Val Gly Ser Gly Thr Ser Tyr Ala Asp Ser Val Lys 1 5 10 15 Gly <![CDATA[<210> 17]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家犬(Canis familiaris)]]> <![CDATA[<400> 17]]> Gly Phe Pro Gly Ser Phe Glu His 1 5 <![CDATA[<210> 18]]> <![CDATA[<211> 312]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> ZTS-5864輕鏈可變區]]> <![CDATA[<400> 18]]> cagtctgtgc tgactcagcc atcctcagtg tctgggaccc taggccagag gatcaccatc 60 tcctgcaccg gaagcagctc caacatcggg agtggttatg tgggctggta tcaacaagtc 120 ccaggaatgg gccccaaaac cgtcatctat tataatagcg accgaccctc tggagtccca 180 gataggttct ccggctccaa gtctggcagc tcaggcaccc tgaccatcac tggattgcag 240 gctgaagacg aggctgacta ttactgttca gtatatgaca gaactttcaa tgctgtgttc 300 ggcggaggga cc 312 <![CDATA[<210> 19]]> <![CDATA[<211> 104]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> ZTS-5864輕鏈可變區]]> <![CDATA[<400> 19]]> Gln Ser Val Leu Thr Gln Pro Ser Ser Val Ser Gly Thr Leu Gly Gln 1 5 10 15 Arg Ile Thr Ile Ser Cys Thr Gly Ser Ser Ser Asn Ile Gly Ser Gly 20 25 30 Tyr Val Gly Trp Tyr Gln Gln Val Pro Gly Met Gly Pro Lys Thr Val 35 40 45 Ile Tyr Tyr Asn Ser Asp Arg Pro Ser Gly Val Pro Asp Arg Phe Ser 50 55 60 Gly Ser Lys Ser Gly Ser Ser Gly Thr Leu Thr Ile Thr Gly Leu Gln 65 70 75 80 Ala Glu Asp Glu Ala Asp Tyr Tyr Cys Ser Val Tyr Asp Arg Thr Phe 85 90 95 Asn Ala Val Phe Gly Gly Gly Thr 100 <![CDATA[<210> 20]]> <![CDATA[<211> 13]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家犬(Canis familiaris)]]> <![CDATA[<400> 20]]> Thr Gly Ser Ser Ser Asn Ile Gly Ser Gly Tyr Val Gly 1 5 10 <![CDATA[<210> 21]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家犬(Canis familiaris)]]> <![CDATA[<400> 21]]> Tyr Tyr Asn Ser Asp Arg Pro 1 5 <![CDATA[<210> 22]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 家犬(Canis familiaris)]]> <![CDATA[<400> 22]]> Ser Val Tyr Asp Arg Thr Phe Asn Ala Val 1 5 10 <![CDATA[<210> 23]]> <![CDATA[<211> 453]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> ZTS768_重_鏈]]> <![CDATA[<400> 23]]> Asp Val Gln Leu Val Glu Ser Gly Gly Asp Leu Val Lys Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Thr Cys Val Ala Ser Gly Phe Thr Tyr Ser Asn Tyr 20 25 30 Trp Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Gln Trp Val 35 40 45 Ala Arg Ile Asp Pro Tyr Gly Gly Gly Thr Lys His Asn Glu Lys Phe 50 55 60 Lys Arg Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Thr Glu Asp Thr Ala Thr Tyr Tyr Cys 85 90 95 Val Arg Ser Gly Tyr Asp Tyr Tyr Phe Asp Val Trp Gly Gln Gly Thr 100 105 110 Leu Val Thr Val Ser Ser Ala Ser Thr Thr Ala Pro Ser Val Phe Pro 115 120 125 Leu Ala Pro Ser Cys Gly Thr Thr Ser Gly Ala Thr Val Ala Leu Ala 130 135 140 Cys Leu Val Leu Gly Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn 145 150 155 160 Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gln 165 170 175 Ala Ser Gly Leu Tyr Ser Leu Ser Ser Met Val Thr Val Pro Ser Ser 180 185 190 Arg Trp Leu Ser Asp Thr Phe Thr Cys Asn Val Ala His Pro Pro Ser 195 200 205 Asn Thr Lys Val Asp Lys Thr Val Arg Lys Thr Asp His Pro Pro Gly 210 215 220 Pro Lys Pro Cys Asp Cys Pro Lys Cys Pro Pro Pro Glu Met Leu Gly 225 230 235 240 Gly Pro Ser Ile Phe Ile Phe Pro Pro Lys Pro Lys Asp Thr Leu Ser 245 250 255 Ile Ser Arg Thr Pro Glu Val Thr Cys Leu Val Val Asp Leu Gly Pro 260 265 270 Asp Asp Ser Asp Val Gln Ile Thr Trp Phe Val Asp Asn Thr Gln Val 275 280 285 Tyr Thr Ala Lys Thr Ser Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr 290 295 300 Arg Val Val Ser Val Leu Pro Ile Leu His Gln Asp Trp Leu Lys Gly 305 310 315 320 Lys Glu Phe Lys Cys Lys Val Asn Ser Lys Ser Leu Pro Ser Pro Ile 325 330 335 Glu Arg Thr Ile Ser Lys Ala Lys Gly Gln Pro His Glu Pro Gln Val 340 345 350 Tyr Val Leu Pro Pro Ala Gln Glu Glu Leu Ser Arg Asn Lys Val Ser 355 360 365 Val Thr Cys Leu Ile Lys Ser Phe His Pro Pro Asp Ile Ala Val Glu 370 375 380 Trp Glu Ile Thr Gly Gln Pro Glu Pro Glu Asn Asn Tyr Arg Thr Thr 385 390 395 400 Pro Pro Gln Leu Asp Ser Asp Gly Thr Tyr Phe Val Tyr Ser Lys Leu 405 410 415 Ser Val Asp Arg Ser His Trp Gln Arg Gly Asn Thr Tyr Thr Cys Ser 420 425 430 Val Ser His Glu Ala Leu His Ser His His Thr Gln Lys Ser Leu Thr 435 440 445 Gln Ser Pro Gly Lys 450 <![CDATA[<210> 24]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 24]]> Asn Tyr Trp Met His 1 5 <![CDATA[<210> 25]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 25]]> Arg Ile Asp Pro Tyr Gly Gly Gly Thr Lys His Asn Glu Lys Phe Lys 1 5 10 15 Arg <![CDATA[<210> 26]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 26]]> Ser Gly Tyr Asp Tyr Tyr Phe Asp Val 1 5 <![CDATA[<210> 27]]> <![CDATA[<211> 217]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> ZTS768_輕_鏈]]> <![CDATA[<400> 27]]> Glu Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Pro Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Glu Asn Ile Tyr Ser Phe 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Val Pro Lys Leu Leu Ile 35 40 45 Tyr Asn Ala Asn Thr Leu Ala Glu Gly Val Pro Ser Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Glu Pro 65 70 75 80 Glu Asp Ala Ala Thr Tyr Tyr Cys Gln His His Phe Gly Thr Pro Phe 85 90 95 Thr Phe Gly Ser Gly Thr Lys Leu Glu Ile Lys Arg Ser Asp Ala Gln 100 105 110 Pro Ser Val Phe Leu Phe Gln Pro Ser Leu Asp Glu Leu His Thr Gly 115 120 125 Ser Ala Ser Ile Val Cys Ile Leu Asn Asp Phe Tyr Pro Lys Glu Val 130 135 140 Asn Val Lys Trp Lys Val Asp Gly Val Val Gln Asn Lys Gly Ile Gln 145 150 155 160 Glu Ser Thr Thr Glu Gln Asn Ser Lys Asp Ser Thr Tyr Ser Leu Ser 165 170 175 Ser Thr Leu Thr Met Ser Ser Thr Glu Tyr Gln Ser His Glu Lys Phe 180 185 190 Ser Cys Glu Val Thr His Lys Ser Leu Ala Ser Thr Leu Val Lys Ser 195 200 205 Phe Gln Arg Ser Glu Cys Gln Arg Glu 210 215 <![CDATA[<210> 28]]> <![CDATA[<211> 11]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 28]]> Arg Ala Ser Glu Asn Ile Tyr Ser Phe Leu Ala 1 5 10 <![CDATA[<210> 29]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 29]]> Asn Ala Asn Thr Leu Ala Glu 1 5 <![CDATA[<210> 30]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 30]]> Gln His His Phe Gly Thr Pro Phe Thr 1 5 <![CDATA[<210> 31]]> <![CDATA[<211> 457]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> NV02_重鏈]]> <![CDATA[<400> 31]]> Gln Val Gln Leu Val Glu Ser Gly Ala Glu Leu Val Gln Pro Gly Glu 1 5 10 15 Ser Leu Arg Leu Thr Cys Ala Ala Ser Gly Phe Ser Leu Thr Asn Asn 20 25 30 Asn Val Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Met 35 40 45 Gly Gly Val Trp Ala Gly Gly Ala Thr Asp Tyr Asn Ser Ala Leu Lys 50 55 60 Ser Arg Leu Thr Ile Thr Arg Asp Thr Ser Lys Asn Thr Val Phe Leu 65 70 75 80 Gln Met His Ser Leu Gln Ser Glu Asp Thr Ala Thr Tyr Tyr Cys Ala 85 90 95 Arg Asp Gly Gly Tyr Ser Ser Ser Thr Leu Tyr Ala Met Asp Ala Trp 100 105 110 Gly Gln Gly Thr Thr Val Thr Val Ser Ala Ala Ser Thr Thr Ala Pro 115 120 125 Ser Val Phe Pro Leu Ala Pro Ser Cys Gly Thr Thr Ser Gly Ala Thr 130 135 140 Val Ala Leu Ala Cys Leu Val Leu Gly Tyr Phe Pro Glu Pro Val Thr 145 150 155 160 Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro 165 170 175 Ala Val Leu Gln Ala Ser Gly Leu Tyr Ser Leu Ser Ser Met Val Thr 180 185 190 Val Pro Ser Ser Arg Trp Leu Ser Asp Thr Phe Thr Cys Asn Val Ala 195 200 205 His Pro Pro Ser Asn Thr Lys Val Asp Lys Thr Val Arg Lys Thr Asp 210 215 220 His Pro Pro Gly Pro Lys Pro Cys Asp Cys Pro Lys Cys Pro Pro Pro 225 230 235 240 Glu Met Leu Gly Gly Pro Ser Ile Phe Ile Phe Pro Pro Lys Pro Lys 245 250 255 Asp Thr Leu Ser Ile Ser Arg Thr Pro Glu Val Thr Cys Leu Val Val 260 265 270 Asp Leu Gly Pro Asp Asp Ser Asp Val Gln Ile Thr Trp Phe Val Asp 275 280 285 Asn Thr Gln Val Tyr Thr Ala Lys Thr Ser Pro Arg Glu Glu Gln Phe 290 295 300 Asn Ser Thr Tyr Arg Val Val Ser Val Leu Pro Ile Leu His Gln Asp 305 310 315 320 Trp Leu Lys Gly Lys Glu Phe Lys Cys Lys Val Asn Ser Lys Ser Leu 325 330 335 Pro Ser Pro Ile Glu Arg Thr Ile Ser Lys Ala Lys Gly Gln Pro His 340 345 350 Glu Pro Gln Val Tyr Val Leu Pro Pro Ala Gln Glu Glu Leu Ser Arg 355 360 365 Asn Lys Val Ser Val Thr Cys Leu Ile Lys Ser Phe His Pro Pro Asp 370 375 380 Ile Ala Val Glu Trp Glu Ile Thr Gly Gln Pro Glu Pro Glu Asn Asn 385 390 395 400 Tyr Arg Thr Thr Pro Pro Gln Leu Asp Ser Asp Gly Thr Tyr Phe Val 405 410 415 Tyr Ser Lys Leu Ser Val Asp Arg Ser His Trp Gln Arg Gly Asn Thr 420 425 430 Tyr Thr Cys Ser Val Ser His Glu Ala Leu His Ser His His Thr Gln 435 440 445 Lys Ser Leu Thr Gln Ser Pro Gly Lys 450 455 <![CDATA[<210> 32]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 黑家鼠(Rattus rattus)]]> <![CDATA[<400> 32]]> Gly Phe Ser Leu Thr Asn Asn Asn Val Asn 1 5 10 <![CDATA[<210> 33]]> <![CDATA[<211> 16]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 黑家鼠(Rattus rattus)]]> <![CDATA[<400> 33]]> Gly Val Trp Ala Gly Gly Ala Thr Asp Tyr Asn Ser Ala Leu Lys Ser 1 5 10 15 <![CDATA[<210> 34]]> <![CDATA[<211> 14]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 黑家鼠(Rattus rattus)]]> <![CDATA[<400> 34]]> Asp Gly Gly Tyr Ser Ser Ser Thr Leu Tyr Ala Met Asp Ala 1 5 10 <![CDATA[<210> 35]]> <![CDATA[<211> 217]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> >NV02_κ鏈]]> <![CDATA[<400> 35]]> Asp Ile Glu Met Thr Gln Ser Pro Leu Ser Leu Ser Val Thr Pro Gly 1 5 10 15 Glu Ser Val Ser Ile Ser Cys Arg Ala Ser Glu Asp Ile Tyr Asn Ala 20 25 30 Leu Ala Trp Tyr Leu Gln Lys Pro Gly Arg Ser Pro Arg Leu Leu Ile 35 40 45 Tyr Asn Thr Asp Thr Leu His Thr Gly Val Pro Asp Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile Ser Arg Val Gln Thr 65 70 75 80 Glu Asp Val Gly Val Tyr Phe Cys Gln His Tyr Phe His Tyr Pro Arg 85 90 95 Thr Phe Gly Gln Gly Thr Lys Leu Glu Leu Lys Arg Ser Asp Ala Gln 100 105 110 Pro Ser Val Phe Leu Phe Gln Pro Ser Leu Asp Glu Leu His Thr Gly 115 120 125 Ser Ala Ser Ile Val Cys Ile Leu Asn Asp Phe Tyr Pro Lys Glu Val 130 135 140 Asn Val Lys Trp Lys Val Asp Gly Val Val Gln Asn Lys Gly Ile Gln 145 150 155 160 Glu Ser Thr Thr Glu Gln Asn Ser Lys Asp Ser Thr Tyr Ser Leu Ser 165 170 175 Ser Thr Leu Thr Met Ser Ser Thr Glu Tyr Gln Ser His Glu Lys Phe 180 185 190 Ser Cys Glu Val Thr His Lys Ser Leu Ala Ser Thr Leu Val Lys Ser 195 200 205 Phe Gln Arg Ser Glu Cys Gln Arg Glu 210 215 <![CDATA[<210> 36]]> <![CDATA[<211> 11]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 黑家鼠(Rattus rattus)]]> <![CDATA[<400> 36]]> Arg Ala Ser Glu Asp Ile Tyr Asn Ala Leu Ala 1 5 10 <![CDATA[<210> 37]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 黑家鼠(Rattus rattus)]]> <![CDATA[<400> 37]]> Asn Thr Asp Thr Leu His Thr 1 5 <![CDATA[<210> 38]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 黑家鼠(Rattus rattus)]]> <![CDATA[<400> 38]]> Gln His Tyr Phe His Tyr Pro Arg Thr 1 5 <![CDATA[<210> 39]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 39]]> Ser Ser Trp Met Asn 1 5 <![CDATA[<210> 40]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 40]]> Gln Ile Tyr Pro Gly Asp Gly Asp Thr Asn Tyr Asn Gly Lys Phe Lys 1 5 10 15 Gly <![CDATA[<210> 41]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 41]]> Ala Arg His Tyr Asp Gly Ser Thr Asp Tyr 1 5 10 <![CDATA[<210> 42]]> <![CDATA[<211> 11]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 42]]> Arg Ala Ser Glu Asn Ile Tyr Ser Asn Leu Ala 1 5 10 <![CDATA[<210> 43]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 43]]> Ala Ala Thr Asn Leu Ala Asp 1 5 <![CDATA[<210> 44]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠(Mus musculus)]]> <![CDATA[<400> 44]]> Gln His Phe Trp Gly Thr Pro Tyr Thr 1 5 <![CDATA[<210> 45]]> <![CDATA[<211> 117]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自小家鼠及家貓之序列的可變重區 ]]> <![CDATA[<400> 45]]> Gln Val Leu Leu Val Gln Ser Gly Ala Glu Val Arg Arg Pro Gly Ala 1 5 10 15 Ser Val Lys Ile Phe Cys Lys Ala Ser Gly Tyr Ser Phe Thr Ser Ser 20 25 30 Trp Met Asn Trp Leu Arg Gln Ala Pro Ala Gln Gly Phe Glu Trp Met 35 40 45 Gly Gln Ile Tyr Pro Gly Asp Gly Asp Thr Asn Tyr Asn Gly Lys Phe 50 55 60 Lys Gly Arg Leu Thr Leu Thr Ala Asp Thr Ser Thr Asp Thr Ala Tyr 65 70 75 80 Met Glu Leu Ser Ser Leu Arg Ser Ala Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg His Tyr Asp Gly Ser Thr Asp Tyr Trp Gly His Gly Thr Ile 100 105 110 Val Thr Val Ser Ser 115 <![CDATA[<210> 46]]> <![CDATA[<211> 351]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自小家鼠及家貓之序列的可變重區 ]]> <![CDATA[<400> 46]]> caggtgctgc tggtgcagag cggcgcggaa gtgcgccgcc cgggcgcgag cgtgaaaatt 60 ttttgcaaag cgagcggcta tagctttacc agcagctgga tgaactggct gcgccaggcg 120 ccggcgcagg gctttgaatg gatgggccag atttatccgg gcgatggcga taccaactat 180 aacggcaaat ttaaaggccg cctgaccctg accgcggata ccagcaccga taccgcgtat 240 atggaactga gcagcctgcg cagcgcggat accgcggtgt attattgcgc gcgccattat 300 gatggcagca ccgattattg gggccatggc accattgtga ccgtgagcag c 351 <![CDATA[<210> 47]]> <![CDATA[<211> 103]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自小家鼠及家貓之序列的可變輕區 ]]> <![CDATA[<400> 47]]> Ala Ile Thr Met Thr Gln Ser Pro Gly Ser Leu Ala Gly Ser Pro Gly 1 5 10 15 Gln Gln Val Thr Met Asn Cys Arg Ala Ser Glu Asn Ile Tyr Ser Asn 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln His Pro Lys Leu Leu Ile 35 40 45 Tyr Ala Ala Thr Asn Leu Ala Asp Gly Val Pro Asp Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Asn Leu Gln Ala 65 70 75 80 Glu Asp Val Ala Ser Tyr Tyr Cys Gln His Phe Trp Gly Thr Pro Tyr 85 90 95 Thr Phe Gly Gly Gly Thr Lys 100 <![CDATA[<210> 48]]> <![CDATA[<211> 309]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自小家鼠及家貓之序列的可變輕區]]> <![CDATA[<400> 48]]> gcgattacca tgacccagag cccgggcagc ctggcgggca gcccgggcca gcaggtgacc 60 atgaactgcc gcgcgagcga aaacatttat agcaacctgg cgtggtatca gcagaaaccg 120 ggccagcatc cgaaactgct gatttatgcg gcgaccaacc tggcggatgg cgtgccggat 180 cgctttagcg gcagcggcag cggcaccgat tttaccctga ccattagcaa cctgcaggcg 240 gaagatgtgg cgagctatta ttgccagcat ttttggggca ccccgtatac ctttggcggc 300 ggcaccaaa 309 <![CDATA[<210> 49]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 49]]> Ser Asn Val Ile Ser 1 5 <![CDATA[<210> 50]]> <![CDATA[<211> 18]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 50]]> Gly Val Ile Pro Ile Val Asp Ile Ala Asn Tyr Ala Gln Arg Phe Lys 1 5 10 15 Gly Arg <![CDATA[<210> 51]]> <![CDATA[<211> 11]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 51]]> Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr 1 5 10 <![CDATA[<210> 52]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 52]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr 1 5 10 <![CDATA[<210> 53]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 53]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 54]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 54]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 55]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 55]]> Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ser 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Tyr Thr Phe Ser Ser Asn 20 25 30 Val Ile Ser Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Gly Val Ile Pro Ile Val Asp Ile Ala Asn Tyr Ala Gln Arg Phe 50 55 60 Lys Gly Arg Val Thr Ile Thr Ala Asp Glu Ser Thr Ser Thr Thr Tyr 65 70 75 80 Met Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ser Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 56]]> <![CDATA[<211> 360]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 56]]> caggtgcagc tggtgcagtc cggagctgag gtgaagaagc caggctccag cgtgaaggtg 60 tcttgcaagg cttccggcta caccttctct tccaacgtga tcagctgggt gagacaggct 120 ccaggacagg gactggagtg gatgggaggc gtgatcccta tcgtggacat cgccaattac 180 gctcagaggt ttaagggccg ggtgaccatc acagctgatg agtccacaag caccacatat 240 atggagctga gctctctgcg cagcgaggac accgccgtgt actattgtgc ttctacactg 300 ggcctggtgc tggacgctat ggactattgg ggccagggca ccctggtgac agtctcgagc 360 <![CDATA[<210> 57]]> <![CDATA[<211> 108]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 57]]> Glu Thr Val Leu Thr Gln Ser Pro Gly Thr Leu Ser Leu Ser Pro Gly 1 5 10 15 Glu Arg Ala Thr Leu Ser Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser 20 25 30 Tyr Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Arg Leu Leu 35 40 45 Ile Tyr Gly Ala Ser Ser Arg Ala Pro Gly Ile Pro Asp Arg Phe Ser 50 55 60 Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Arg Leu Glu 65 70 75 80 Pro Glu Asp Phe Ala Val Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro 85 90 95 Ile Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 58]]> <![CDATA[<211> 324]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 58]]> gagaccgtgc tgacacagtc tcctggcacc ctgagcctgt ctccaggaga gagggccaca 60 ctgtcctgca gggcttccca gagcctgggc tccagctacc tggcctggta tcagcagaag 120 ccaggccagg ctcccaggct gctgatctac ggagcctctt ccagagctcc aggcatccct 180 gaccgcttct ctggatccgg aagcggcacc gacttcaccc tgacaatcag cagactggag 240 cccgaggact tcgccgtgta ctattgtcag cagtatgctg attctcctat cacatttggc 300 cagggtacca agctggagat caaa 324 <![CDATA[<210> 59]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 59]]> Ser Asn Val Ile Ser 1 5 <![CDATA[<210> 60]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 60]]> Gly Val Ile Pro Ile Val Asp Ile Ala Asn Tyr Ala Gln Arg Phe Lys 1 5 10 15 Gly <![CDATA[<210> 61]]> <![CDATA[<211> 13]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 61]]> Ala Ser Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr 1 5 10 <![CDATA[<210> 62]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 62]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr 1 5 10 <![CDATA[<210> 63]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 63]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 64]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 64]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 65]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 65]]> Gln Val Leu Leu Val Gln Ser Gly Ala Asp Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Ile Phe Cys Lys Ala Ser Gly Tyr Thr Phe Thr Ser Asn 20 25 30 Val Ile Ser Trp Val Arg Gln Thr Pro Ala Gln Gly Phe Glu Trp Met 35 40 45 Gly Gly Val Ile Pro Ile Val Asp Ile Ala Asn Tyr Ala Gln Arg Phe 50 55 60 Lys Gly Arg Leu Val Leu Thr Ala Asp Thr Ser Thr Asn Thr Ala Tyr 65 70 75 80 Met Glu Leu Arg Ser Leu Lys Ser Ala Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ser Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Ser Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 66]]> <![CDATA[<211> 360]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 66]]> caggtgctgc tggtgcagtc tggcgccgat gtgagaaagc caggcgctag cgtgaagatc 60 ttctgcaagg cctctggcta cacctttaca tctaacgtga tctcctgggt gcgccagaca 120 ccagctcagg gattcgagtg gatgggaggc gtgatcccta tcgtggacat cgccaactac 180 gctcagaggt ttaagggccg gctggtgctg accgctgata cctccacaaa taccgcttat 240 atggagctga ggtccctgaa gagcgccgac acagccgtgt actattgtgc ctccaccctg 300 ggactggtgc tggacgctat ggattattgg ggccagggca gcctggtgac agtctcgagc 360 <![CDATA[<210> 67]]> <![CDATA[<211> 108]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 67]]> Glu Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Pro Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser 20 25 30 Tyr Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Val Pro Lys Leu Leu 35 40 45 Ile Tyr Gly Ala Ser Ser Arg Ala Pro Gly Val Pro Ser Arg Phe Ser 50 55 60 Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Glu 65 70 75 80 Pro Glu Asp Ala Ala Thr Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro 85 90 95 Ile Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 68]]> <![CDATA[<211> 324]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 68]]> gagatccaga tgacccagtc tccttccagc ctgtctgcct ccccaggcga cagggtgacc 60 atcacatgcc gggccagcca gtctctgggc tcttcctacc tggcttggta tcagcagaag 120 ccaggcaagg tgcccaagct gctgatctac ggagccagct ctagagctcc aggcgtgcct 180 tcccgcttct ccggaagcgg atctggcaca gacttcaccc tgacaatctc cagcctggag 240 ccagaggacg ctgctaccta ctattgtcag cagtatgctg atagccctat cacattcggc 300 cagggtacca agctggagat caaa 324 <![CDATA[<210> 69]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 69]]> Ser Asn Val Ile Ser 1 5 <![CDATA[<210> 70]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 70]]> Gly Val Ile Pro Ile Val Asp Ile Ala Asn Tyr Ala Gln Arg Phe Lys 1 5 10 15 Gly <![CDATA[<210> 71]]> <![CDATA[<211> 13]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 71]]> Ala Ser Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr 1 5 10 <![CDATA[<210> 72]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 72]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr Leu Ala 1 5 10 <![CDATA[<210> 73]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 73]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 74]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 74]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 75]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 75]]> Gln Val Leu Leu Val Gln Ser Gly Ala Glu Val Arg Thr Pro Gly Ala 1 5 10 15 Ser Val Lys Ile Phe Cys Lys Ala Ser Gly Tyr Gly Phe Thr Ser Asn 20 25 30 Val Ile Ser Trp Val Arg Gln Ser Pro Ala Gln Gly Leu Glu Trp Met 35 40 45 Gly Gly Val Ile Pro Ile Val Asp Ile Ala Asn Tyr Ala Gln Arg Phe 50 55 60 Lys Gly Arg Leu Thr Leu Thr Ala Asp Thr Ser Thr Asp Thr Ala Tyr 65 70 75 80 Met Glu Leu Ser Ser Leu Arg Ser Ala Asp Thr Ala Met Tyr Tyr Cys 85 90 95 Ala Ser Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 76]]> <![CDATA[<211> 363]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 76]]> caggtgctgc tggtgcagtc tggcgccgag gtgagaacac caggcgctag cgtgaagatc 60 ttctgcaagg cctctggcta cggctttacc tctaacgtga tctcctgggt gcgccagtcc 120 ccagctcagg gactggagtg gatgggaggc gtgatcccta tcgtggacat cgccaattac 180 gctcagaggt tcaagggccg gctgaccctg acagctgaca cctccacaga taccgcttat 240 atggagctgt ccagcctgag gtccgccgat acagctatgt actattgtgc cagcaccctg 300 ggactggtgc tggacgctat ggattattgg ggccagggca cactggtgac cgtggtctcg 360 agc 363 <![CDATA[<210> 77]]> <![CDATA[<211> 108]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 77]]> Glu Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Pro Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser 20 25 30 Tyr Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Val Pro Lys Leu Leu 35 40 45 Ile Tyr Gly Ala Ser Ser Arg Ala Pro Gly Val Pro Ser Arg Phe Ser 50 55 60 Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Glu 65 70 75 80 Pro Glu Asp Ala Ala Thr Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro 85 90 95 Ile Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 78]]> <![CDATA[<211> 324]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 78]]> gagatccaga tgacccagtc tccttccagc ctgtctgcct ccccaggcga cagggtgacc 60 atcacatgcc gggccagcca gtctctgggc tcttcctacc tggcttggta tcagcagaag 120 ccaggcaagg tgcccaagct gctgatctac ggagccagct ctagagctcc aggcgtgcct 180 tcccgcttct ccggaagcgg atctggcaca gacttcaccc tgacaatctc cagcctggag 240 ccagaggacg ctgctaccta ctattgtcag cagtatgctg atagccctat cacattcggc 300 cagggtacca agctggagat caaa 324 <![CDATA[<210> 79]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 79]]> Gly Tyr Thr Phe Ser Ser Asn Val 1 5 <![CDATA[<210> 80]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 80]]> Val Ile Pro Ile Val Asp Ile Ala 1 5 <![CDATA[<210> 81]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 81]]> Leu Gly Leu Val Leu Asp Ala Met Asp Tyr 1 5 10 <![CDATA[<210> 82]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 82]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr Leu Ala 1 5 10 <![CDATA[<210> 83]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 83]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 84]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 84]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 85]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 85]]> Gln Val Leu Leu Val Gln Ser Gly Ala Asp Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Ile Phe Cys Lys Ala Ser Gly Tyr Thr Phe Ser Ser Asn 20 25 30 Val Met His Trp Val Arg Gln Thr Pro Ala Gln Gly Phe Glu Trp Met 35 40 45 Gly Ser Val Ile Pro Ile Val Asp Ile Ala Thr Tyr Ala Arg Arg Phe 50 55 60 Gln Gly Arg Leu Val Leu Thr Ala Asp Thr Ser Thr Asn Thr Ala Tyr 65 70 75 80 Met Glu Leu Arg Ser Leu Lys Ser Ala Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Ser Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 86]]> <![CDATA[<211> 360]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 86]]> caggtgctgc tggtgcagtc tggcgccgat gtgaggaagc caggcgctag cgtgaagatc 60 ttctgcaagg cctctggcta cacattttcc agcaacgtga tgcactgggt gagacagacc 120 cccgctcagg gcttcgagtg gatgggctcc gtgatcccta tcgtggacat cgccacatac 180 gctaggcggt ttcagggcag gctggtgctg accgccgata ccagcacaaa taccgcttat 240 atggagctga gatctctgaa gtccgccgac acagccgtgt actattgtgc tcgcaccctg 300 ggactggtgc tggacgctat ggattattgg ggccagggct ccctggtgac agtctcgagc 360 <![CDATA[<210> 87]]> <![CDATA[<211> 108]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 87]]> Glu Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Pro Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser 20 25 30 Tyr Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Val Pro Lys Leu Leu 35 40 45 Ile Tyr Gly Ala Ser Ser Arg Ala Pro Gly Val Pro Ser Arg Phe Ser 50 55 60 Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Glu 65 70 75 80 Pro Glu Asp Ala Ala Thr Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro 85 90 95 Ile Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 88]]> <![CDATA[<211> 324]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 88]]> gagatccaga tgacccagtc tccttccagc ctgtctgcct ccccaggcga cagggtgacc 60 atcacatgcc gggccagcca gtctctgggc tcttcctacc tggcttggta tcagcagaag 120 ccaggcaagg tgcccaagct gctgatctac ggagccagct ctagagctcc aggcgtgcct 180 tcccgcttct ccggaagcgg atctggcaca gacttcaccc tgacaatctc cagcctggag 240 ccagaggacg ctgctaccta ctattgtcag cagtatgctg atagccctat cacattcggc 300 cagggtacca agctggagat caaa 324 <![CDATA[<210> 89]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 89]]> Gly Tyr Thr Phe Ser Ser Asn Val 1 5 <![CDATA[<210> 90]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 90]]> Val Ile Pro Ile Val Asp Ile Ala 1 5 <![CDATA[<210> 91]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 91]]> Leu Val Leu Asp Ala Met Asp Tyr 1 5 <![CDATA[<210> 92]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 92]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr Leu Ala 1 5 10 <![CDATA[<210> 93]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 93]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 94]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 94]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 95]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 95]]> Asp Val Gln Leu Val Glu Ser Gly Gly Asp Leu Val Lys Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Thr Cys Val Ala Ser Gly Tyr Thr Phe Ser Ser Asn 20 25 30 Val Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Gln Trp Val 35 40 45 Ala Tyr Val Ile Pro Ile Val Asp Ile Ala Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Ile Asp Asn Ser Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Thr Glu Asp Thr Ala Thr Tyr Tyr Cys 85 90 95 Ala Arg Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 96]]> <![CDATA[<211> 360]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 96]]> gacgtgcagc tggtggagtc tggaggcgat ctggtgaagc caggaggcag cctgaggctg 60 acctgcgtgg cttctggcta cacattctcc agcaacgtga tgcactgggt gcggcaggct 120 ccaggcaagg gactgcagtg ggtggcttat gtgatcccta tcgtggacat cgcctactat 180 gctgattccg tgaagggcag gttcaccatc tctatcgaca actccaagaa tacactgtac 240 ctgcagatga atagcctgaa gaccgaggat accgccacat actattgtgc tcgcacactg 300 ggcctggtgc tggacgctat ggattattgg ggccagggca ccctggtgac agtctcgagc 360 <![CDATA[<210> 97]]> <![CDATA[<211> 108]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 97]]> Glu Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Pro Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser 20 25 30 Tyr Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Val Pro Lys Leu Leu 35 40 45 Ile Tyr Gly Ala Ser Ser Arg Ala Pro Gly Val Pro Ser Arg Phe Ser 50 55 60 Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Glu 65 70 75 80 Pro Glu Asp Ala Ala Thr Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro 85 90 95 Ile Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 98]]> <![CDATA[<211> 324]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 98]]> gagatccaga tgacccagtc tccttccagc ctgtctgcct ccccaggcga cagggtgacc 60 atcacatgcc gggccagcca gtctctgggc tcttcctacc tggcttggta tcagcagaag 120 ccaggcaagg tgcccaagct gctgatctac ggagccagct ctagagctcc aggcgtgcct 180 tcccgcttct ccggaagcgg atctggcaca gacttcaccc tgacaatctc cagcctggag 240 ccagaggacg ctgctaccta ctattgtcag cagtatgctg atagccctat cacattcggc 300 cagggtacca agctggagat caaa 324 <![CDATA[<210> 99]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 99]]> Gly Tyr Thr Phe Ser Ser Asn Val 1 5 <![CDATA[<210> 100]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 100]]> Val Ile Pro Ile Val Asp Ile Ala 1 5 <![CDATA[<210> 101]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 101]]> Leu Gly Leu Val Leu Asp Ala Met Asp Tyr 1 5 10 <![CDATA[<210> 102]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 102]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr Leu Ala 1 5 10 <![CDATA[<210> 103]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 103]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 104]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 104]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 105]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區]]> <![CDATA[<400> 105]]> Gln Val Leu Leu Val Gln Ser Gly Ala Asp Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Ile Phe Cys Lys Ala Ser Gly Tyr Thr Phe Ser Ser Asn 20 25 30 Val Met His Trp Val Arg Gln Thr Pro Ala Gln Gly Phe Glu Trp Met 35 40 45 Gly Ser Val Ile Pro Ile Val Asp Ile Ala Thr Tyr Ala Arg Arg Phe 50 55 60 Gln Gly Arg Leu Val Leu Thr Ala Asp Thr Ser Thr Asn Thr Ala Tyr 65 70 75 80 Met Glu Leu Arg Ser Leu Lys Ser Ala Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Arg Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Ser Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 106]]> <![CDATA[<211> 360]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 106]]> caggtgctgc tggtgcagtc tggcgccgat gtgaggaagc caggcgctag cgtgaagatc 60 ttctgcaagg cctctggcta cacattttcc agcaacgtga tgcactgggt gagacagacc 120 cccgctcagg gcttcgagtg gatgggctcc gtgatcccta tcgtggacat cgccacatac 180 gctaggcggt ttcagggcag gctggtgctg accgccgata ccagcacaaa taccgcttat 240 atggagctga gatctctgaa gtccgccgac acagccgtgt actattgtgc tcgcaccctg 300 ggactggtgc tggacgctat ggattattgg ggccagggct ccctggtgac agtctcgagc 360 <![CDATA[<210> 107]]> <![CDATA[<211> 107]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 107]]> Asp Ile Val Leu Thr Gln Pro Pro Ser Leu Ser Val Asn Leu Gly Gln 1 5 10 15 Thr Ala Arg Ile Thr Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Lys Leu Val Thr 35 40 45 Tyr Gly Ala Ser Ser Arg Ala Pro Gly Ile Pro Asp Arg Phe Ser Gly 50 55 60 Thr Asn Ser Gly Ile Thr Ala Thr Leu Thr Ile Ser Gly Ala Arg Ala 65 70 75 80 Glu Asp Glu Ala Asp Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro Ile 85 90 95 Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 108]]> <![CDATA[<211> 321]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 108]]> gacatcgtgc tgacacagcc ccctagcctg tctgtgaacc tgggacagac agctaggatc 60 acctgcaggg cttcccagag cctgggctcc agctacctgg cctggtatca gcagaagcct 120 ggccaggctc caaagctggt gacatacggc gcctcttcca gagctccagg catccccgac 180 cgcttctctg gcaccaattc cggcatcacc gccacactga ccatcagcgg agccagggct 240 gaggacgagg ctgattacta ttgtcagcag tatgctgatt ctcccatcac ctttggccag 300 ggtaccaagc tggagatcaa a 321 <![CDATA[<210> 109]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 109]]> Gly Tyr Thr Phe Ser Ser Asn Val 1 5 <![CDATA[<210> 110]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 110]]> Val Ile Pro Ile Val Asp Ile Ala 1 5 <![CDATA[<210> 111]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 111]]> Leu Val Leu Asp Ala Met Asp Tyr 1 5 <![CDATA[<210> 112]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 112]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr Leu Ala 1 5 10 <![CDATA[<210> 113]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 113]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 114]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 114]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 115]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 115]]> Asp Val Gln Leu Val Glu Ser Gly Gly Asp Leu Val Lys Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Thr Cys Val Ala Ser Gly Tyr Thr Phe Ser Ser Asn 20 25 30 Val Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Gln Trp Val 35 40 45 Ala Tyr Val Ile Pro Ile Val Asp Ile Ala Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Ile Asp Asn Ser Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Thr Glu Asp Thr Ala Thr Tyr Tyr Cys 85 90 95 Ala Arg Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 116]]> <![CDATA[<211> 360]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區]]> <![CDATA[<400> 116]]> gacgtgcagc tggtggagtc tggaggcgat ctggtgaagc caggaggcag cctgaggctg 60 acctgcgtgg cttctggcta cacattctcc agcaacgtga tgcactgggt gcggcaggct 120 ccaggcaagg gactgcagtg ggtggcttat gtgatcccta tcgtggacat cgcctactat 180 gctgattccg tgaagggcag gttcaccatc tctatcgaca actccaagaa tacactgtac 240 ctgcagatga atagcctgaa gaccgaggat accgccacat actattgtgc tcgcacactg 300 ggcctggtgc tggacgctat ggattattgg ggccagggca ccctggtgac agtctcgagc 360 <![CDATA[<210> 117]]> <![CDATA[<211> 107]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 117]]> Asp Ile Val Leu Thr Gln Pro Pro Ser Leu Ser Val Asn Leu Gly Gln 1 5 10 15 Thr Ala Arg Ile Thr Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Lys Leu Val Thr 35 40 45 Tyr Gly Ala Ser Ser Arg Ala Pro Gly Ile Pro Asp Arg Phe Ser Gly 50 55 60 Thr Asn Ser Gly Ile Thr Ala Thr Leu Thr Ile Ser Gly Ala Arg Ala 65 70 75 80 Glu Asp Glu Ala Asp Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro Ile 85 90 95 Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 118]]> <![CDATA[<211> 321]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 118]]> gacatcgtgc tgacacagcc ccctagcctg tctgtgaacc tgggacagac agctaggatc 60 acctgcaggg cttcccagag cctgggctcc agctacctgg cctggtatca gcagaagcct 120 ggccaggctc caaagctggt gacatacggc gcctcttcca gagctccagg catccccgac 180 cgcttctctg gcaccaattc cggcatcacc gccacactga ccatcagcgg agccagggct 240 gaggacgagg ctgattacta ttgtcagcag tatgctgatt ctcccatcac ctttggccag 300 ggtaccaagc tggagatcaa a 321 <![CDATA[<210> 119]]> <![CDATA[<211> 5]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 119]]> Ser Asn Val Ile Ser 1 5 <![CDATA[<210> 120]]> <![CDATA[<211> 17]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 120]]> Gly Val Ile Pro Ile Val Asp Ile Ala Asn Tyr Ala Gln Arg Phe Lys 1 5 10 15 Gly <![CDATA[<210> 121]]> <![CDATA[<211> 13]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 121]]> Ala Ser Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr 1 5 10 <![CDATA[<210> 122]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 122]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr Leu Ala 1 5 10 <![CDATA[<210> 123]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 123]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 124]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 124]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 125]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 125]]> Gln Val Leu Leu Val Gln Ser Gly Ala Asp Val Arg Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Ile Phe Cys Lys Ala Ser Gly Tyr Thr Phe Thr Ser Asn 20 25 30 Val Ile Ser Trp Val Arg Gln Thr Pro Ala Gln Gly Phe Glu Trp Met 35 40 45 Gly Gly Val Ile Pro Ile Val Asp Ile Ala Asn Tyr Ala Gln Arg Phe 50 55 60 Lys Gly Arg Leu Val Leu Thr Ala Asp Thr Ser Thr Asn Thr Ala Tyr 65 70 75 80 Met Glu Leu Arg Ser Leu Lys Ser Ala Asp Thr Ala Val Tyr Tyr Cys 85 90 95 Ala Ser Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Ser Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 126]]> <![CDATA[<211> 360]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 126]]> caggtgctgc tggtgcagtc tggcgccgat gtgagaaagc caggcgctag cgtgaagatc 60 ttctgcaagg cctctggcta cacctttaca tctaacgtga tctcctgggt gcgccagaca 120 ccagctcagg gattcgagtg gatgggaggc gtgatcccta tcgtggacat cgccaactac 180 gctcagaggt ttaagggccg gctggtgctg accgctgata cctccacaaa taccgcttat 240 atggagctga ggtccctgaa gagcgccgac acagccgtgt actattgtgc ctccaccctg 300 ggactggtgc tggacgctat ggattattgg ggccagggca gcctggtgac agtctcgagc 360 <![CDATA[<210> 127]]> <![CDATA[<211> 108]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 127]]> Asp Ile Val Met Thr Gln Ser Pro Gly Ser Leu Ala Gly Ser Pro Gly 1 5 10 15 Gln Gln Val Thr Met Asn Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser 20 25 30 Tyr Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln His Pro Glu Leu Leu 35 40 45 Ile Tyr Gly Ala Ser Ser Arg Ala Pro Gly Val Pro Asp Arg Phe Ser 50 55 60 Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Asn Leu Gln 65 70 75 80 Ala Glu Asp Val Ala Asn Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro 85 90 95 Ile Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 128]]> <![CDATA[<211> 324]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 128]]> gacatcgtga tgacccagtc ccctggcagc ctggctggaa gcccaggaca gcaggtgaca 60 atgaactgca gggccagcca gtctctgggc tccagctacc tggcttggta tcagcagaag 120 ccaggccagc accccgagct gctgatctac ggagcctctt ccagggctcc aggcgtgcct 180 gaccggttct ccggaagcgg atctggcacc gacttcaccc tgacaatctc taacctgcag 240 gccgaggacg tggctaatta ctattgtcag cagtatgctg attcccccat cacattcggc 300 cagggtacca agctggagat caaa 324 <![CDATA[<210> 129]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 129]]> Gly Tyr Thr Phe Ser Ser Asn Val 1 5 <![CDATA[<210> 130]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 130]]> Val Ile Pro Ile Val Asp Ile Ala 1 5 <![CDATA[<210> 131]]> <![CDATA[<211> 8]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 131]]> Leu Val Leu Asp Ala Met Asp Tyr 1 5 <![CDATA[<210> 132]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 132]]> Arg Ala Ser Gln Ser Leu Gly Ser Ser Tyr Leu Ala 1 5 10 <![CDATA[<210> 133]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 133]]> Gly Ala Ser Ser Arg Ala Pro 1 5 <![CDATA[<210> 134]]> <![CDATA[<211> 9]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 134]]> Gln Gln Tyr Ala Asp Ser Pro Ile Thr 1 5 <![CDATA[<210> 135]]> <![CDATA[<211> 120]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 135]]> Asp Val Gln Leu Val Glu Ser Gly Gly Asp Leu Val Lys Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Thr Cys Val Ala Ser Gly Tyr Thr Phe Ser Ser Asn 20 25 30 Val Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Gln Trp Val 35 40 45 Ala Tyr Val Ile Pro Ile Val Asp Ile Ala Tyr Tyr Ala Asp Ser Val 50 55 60 Lys Gly Arg Phe Thr Ile Ser Ile Asp Asn Ser Lys Asn Thr Leu Tyr 65 70 75 80 Leu Gln Met Asn Ser Leu Lys Thr Glu Asp Thr Ala Thr Tyr Tyr Cys 85 90 95 Ala Arg Thr Leu Gly Leu Val Leu Asp Ala Met Asp Tyr Trp Gly Gln 100 105 110 Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 136]]> <![CDATA[<211> 360]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變重區 ]]> <![CDATA[<400> 136]]> gacgtgcagc tggtggagtc tggaggcgat ctggtgaagc caggaggcag cctgaggctg 60 acctgcgtgg cttctggcta cacattctcc agcaacgtga tgcactgggt gcggcaggct 120 ccaggcaagg gactgcagtg ggtggcttat gtgatcccta tcgtggacat cgcctactat 180 gctgattccg tgaagggcag gttcaccatc tctatcgaca actccaagaa tacactgtac 240 ctgcagatga atagcctgaa gaccgaggat accgccacat actattgtgc tcgcacactg 300 ggcctggtgc tggacgctat ggattattgg ggccagggca ccctggtgac agtctcgagc 360 <![CDATA[<210> 137]]> <![CDATA[<211> 108]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 137]]> Asp Ile Val Met Thr Gln Ser Pro Gly Ser Leu Ala Gly Ser Pro Gly 1 5 10 15 Gln Gln Val Thr Met Asn Cys Arg Ala Ser Gln Ser Leu Gly Ser Ser 20 25 30 Tyr Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln His Pro Glu Leu Leu 35 40 45 Ile Tyr Gly Ala Ser Ser Arg Ala Pro Gly Val Pro Asp Arg Phe Ser 50 55 60 Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Asn Leu Gln 65 70 75 80 Ala Glu Asp Val Ala Asn Tyr Tyr Cys Gln Gln Tyr Ala Asp Ser Pro 85 90 95 Ile Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 <![CDATA[<210> 138]]> <![CDATA[<211> 324]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 貓類化序列 - 經工程改造以具有來自智人及家貓之序列的可變輕區 ]]> <![CDATA[<400> 138]]> gacatcgtga tgacccagtc ccctggcagc ctggctggaa gcccaggaca gcaggtgaca 60 atgaactgca gggccagcca gtctctgggc tccagctacc tggcttggta tcagcagaag 120 ccaggccagc accccgagct gctgatctac ggagcctctt ccagggctcc aggcgtgcct 180 gaccggttct ccggaagcgg atctggcacc gacttcaccc tgacaatctc taacctgcag 240 gccgaggacg tggctaatta ctattgtcag cagtatgctg attcccccat cacattcggc 300 cagggtacca agctggagat caaa 324
Claims (46)
- 一種經修飾之IgG,其包含貓IgG恆定域,該貓IgG恆定域相對於野生型貓IgG恆定域包含至少二個胺基酸取代,其中該至少二個胺基酸取代係根據如Kabat之EU索引編號的位置428之絲胺酸經白胺酸取代(S428L)和位置434之絲胺酸經組胺酸取代(S434H)。
- 如請求項1之經修飾之IgG,其中與具有該野生型貓IgG恆定域之IgG之半衰期相比,該經修飾之IgG具有延長的半衰期。
- 如請求項1之經修飾之IgG,其中相比於具有該野生型貓IgG恆定域之IgG,該經修飾之IgG具有對FcRn之較高親和力。
- 如請求項1之經修飾之IgG,其中該經修飾之IgG為貓或貓類化IgG。
- 如請求項1之經修飾之IgG,其中該IgG為IgG1a、IgG1b或IgG2。
- 如請求項1之經修飾之IgG,其中該IgG恆定域為IgG1a、IgG1b或IgG2之恆定域。
- 如請求項1之經修飾之IgG,其中該IgG恆定域包含具有CH3域之Fc恆定區。
- 如請求項1之經修飾之IgG,其中該IgG恆定域包含具有CH2及CH3域之Fc恆定區。
- 一種醫藥組合物,其包含如請求項1至8中任一項之經修飾之IgG及醫藥學上可接受之載劑。
- 一種套組,其包含於容器中之如請求項1至8中任一項之經修飾之IgG及使用說明書。
- 一種多肽,其包含貓IgG恆定域,該貓IgG恆定域相對於野生型貓IgG恆定域包含至少二個胺基酸取代,其中該至少二個胺基酸取代係根據如Kabat之EU索引編號的位置428之絲胺酸經白胺酸取代(S428L)和位置434之絲胺酸經組胺酸取代(S434H)。
- 如請求項11之多肽,其中與該野生型貓IgG恆定域之多肽之半衰期相比,該多肽具有延長的半衰期。
- 如請求項11之多肽,其中與具有該野生型貓IgG恆定域之IgG之多肽相比,該多肽具有對FcRn之較高親和力。
- 如請求項11之多肽,其中該多肽為貓或貓類化IgG之多肽。
- 如請求項14之多肽,其中該IgG為IgG1a、IgG1b或IgG2。
- 如請求項11之多肽,其中該IgG恆定域為IgG1a、IgG1b或IgG2之恆定域。
- 如請求項11之多肽,其中該IgG恆定域包含具有CH3域之Fc恆定區。
- 如請求項11之多肽,其中該IgG恆定域包含具有CH2及CH3域之Fc恆定區。
- 一種醫藥組合物,其包含如請求項11至 18中任一項之多肽及醫藥學上可接受之載劑。
- 一種套組,其包含於容器中之如請求項11至18中任一項之多肽及使用說明書。
- 一種抗體,其包含貓IgG恆定域,該貓IgG恆定域相對於野生型貓IgG恆定域包含至少二個胺基酸取代,其中該至少二個胺基酸取代係根據如Kabat之EU索引編號的位置428之絲胺酸經白胺酸取代(S428L)和位置434之絲胺酸經組胺酸取代(S434H)。
- 如請求項21之抗體,其中與具有該野生型貓IgG恆定域之抗體之半衰期相比,該抗體具有延長的半衰期。
- 如請求項21之抗體,其中與具有該野生型貓IgG恆定域之抗體相比,該抗體具有對FcRn之較高親和力。
- 如請求項21之抗體,其中該抗體為貓或貓類化抗體。
- 如請求項21之抗體,其中該抗體為IgG1a、IgG1b或IgG2。
- 如請求項21之抗體,其中該IgG恆定域為IgG1a、IgG1b或IgG2之恆定域。
- 如請求項21之抗體,其中該IgG恆定域包含具有CH3域之Fc恆定區。
- 如請求項21之抗體,其中該IgG恆定域包含具有CH2及CH3域之Fc恆定區。
- 一種醫藥組合物,其包含如請求項21至28中任一項之抗體及醫藥學上可接受之載劑。
- 一種套組,其包含於容器中之如請求項21至28中任一項之抗體及使用說明書。
- 一種載體,其包含核酸序列,該核酸序列編碼如請求項21至28中任一項之抗體之胺基酸序列。
- 一種經分離之細胞,其包含如請求項31之載體。
- 一種製造如請求項21至28中任一項之抗體之方法,該方法包含:提供如請求項32之細胞;及培養該細胞。
- 一種如請求項21至28中任一項之抗體於製造藥物或套組之用途,該藥物或套組係用於延長貓之抗體血清半衰期。
- 如請求項34之用途,其中與具有該野生型貓IgG恆定域之抗體之半衰期相比,該抗體具有延長的半衰期。
- 如請求項34之用途,其中與具有該野生型貓IgG恆定域之抗體相比,該抗體具有對FcRn之較高親和力。
- 如請求項34之用途,其中該抗體為貓或貓類化抗體。
- 如請求項34之用途,其中該抗體為IgG1a、IgG1b或IgG2。
- 如請求項34之用途,其中該IgG恆定域為IgG1a、IgG1b或IgG2之恆定域。
- 如請求項34之用途,其中該IgG恆定域包含具有CH3域之Fc恆定區。
- 如請求項34之用途,其中該IgG恆定域包含具有CH2及CH3域之Fc恆定區。
- 如請求項21至28中任一項之抗體,其中該抗體為抗TGFβ抗體。
- 如請求項29之醫藥組合物,其中該抗體為抗TGFβ抗體。
- 如請求項30之套組,其中該抗體為抗TGFβ抗體。
- 如請求項33之方法,其中該抗體為抗TGFβ抗體。
- 如請求項34至41中任一項之用途,其中該抗體為抗TGFβ抗體。
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020082048A1 (en) * | 2018-10-18 | 2020-04-23 | Kindred Biosciences, Inc. | Fc variants with altered binding to neonatal fc receptor (fcrn) for veterinary use |
WO2020116560A1 (ja) * | 2018-12-05 | 2020-06-11 | 株式会社バイカ・セラピュティクス | 抗体のFc領域改変体 |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8308235D0 (en) | 1983-03-25 | 1983-05-05 | Celltech Ltd | Polypeptides |
US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
US5807715A (en) | 1984-08-27 | 1998-09-15 | The Board Of Trustees Of The Leland Stanford Junior University | Methods and transformed mammalian lymphocyte cells for producing functional antigen-binding protein including chimeric immunoglobulin |
GB8422238D0 (en) | 1984-09-03 | 1984-10-10 | Neuberger M S | Chimeric proteins |
US5225539A (en) | 1986-03-27 | 1993-07-06 | Medical Research Council | Recombinant altered antibodies and methods of making altered antibodies |
US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
US5530101A (en) | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
US6284471B1 (en) | 1991-03-18 | 2001-09-04 | New York University Medical Center | Anti-TNFa antibodies and assays employing anti-TNFa antibodies |
US5698762A (en) | 1994-12-09 | 1997-12-16 | Dauerman; Leonard | Microwave-assisted pyrolysis of waste polyaromatic hydrocarbons |
US20030031671A1 (en) | 2001-08-01 | 2003-02-13 | Sydney Welt | Methods of treating colon cancer utilizing tumor-specific antibodies |
KR20070057839A (ko) | 2004-08-19 | 2007-06-07 | 제넨테크, 인크. | 변경된 이펙터 기능을 갖는 폴리펩티드 변이체 |
US8367805B2 (en) | 2004-11-12 | 2013-02-05 | Xencor, Inc. | Fc variants with altered binding to FcRn |
AU2005304624B2 (en) | 2004-11-12 | 2010-10-07 | Xencor, Inc. | Fc variants with altered binding to FcRn |
US8546543B2 (en) | 2004-11-12 | 2013-10-01 | Xencor, Inc. | Fc variants that extend antibody half-life |
EP4269443A3 (en) * | 2007-12-26 | 2023-12-27 | Xencor, Inc. | Fc variants with altered binding to fcrn |
ES2665954T3 (es) | 2010-08-19 | 2018-04-30 | Zoetis Belgium S.A. | Anticuerpos anti-NGF y su uso |
US8790651B2 (en) | 2011-07-21 | 2014-07-29 | Zoetis Llc | Interleukin-31 monoclonal antibody |
WO2013184871A1 (en) | 2012-06-06 | 2013-12-12 | Zoetis Llc | Caninized anti-ngf antibodies and methods thereof |
WO2019113123A1 (en) * | 2017-12-04 | 2019-06-13 | Precithera, Inc. | TGF-ß RECEPTOR FUSION PROTEINS AND OTHER TGF-ß ANTAGONISTS FOR REDUCING TGF-ß SIGNALING |
IL297290A (en) * | 2020-04-17 | 2022-12-01 | Zoetis Services Llc | Feline antibody variants |
-
2021
- 2021-09-29 US US18/246,725 patent/US20230382986A1/en active Pending
- 2021-09-29 JP JP2023519633A patent/JP2023542737A/ja active Pending
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- 2021-09-29 AU AU2021352395A patent/AU2021352395A1/en active Pending
- 2021-09-29 KR KR1020237014648A patent/KR20230091914A/ko unknown
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2023
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- 2023-04-25 EC ECSENADI202330307A patent/ECSP23030307A/es unknown
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020082048A1 (en) * | 2018-10-18 | 2020-04-23 | Kindred Biosciences, Inc. | Fc variants with altered binding to neonatal fc receptor (fcrn) for veterinary use |
WO2020116560A1 (ja) * | 2018-12-05 | 2020-06-11 | 株式会社バイカ・セラピュティクス | 抗体のFc領域改変体 |
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US20230382986A1 (en) | 2023-11-30 |
CA3195049A1 (en) | 2022-04-07 |
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CL2023000914A1 (es) | 2023-10-20 |
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CL2024000789A1 (es) | 2024-07-19 |
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TW202413413A (zh) | 2024-04-01 |
WO2022072446A1 (en) | 2022-04-07 |
KR20230091914A (ko) | 2023-06-23 |
CN116457369A (zh) | 2023-07-18 |
AU2021352395A1 (en) | 2023-04-27 |
CO2023004107A2 (es) | 2023-04-27 |
PE20240110A1 (es) | 2024-01-22 |
JP2023542737A (ja) | 2023-10-11 |
IL301414A (en) | 2023-05-01 |
TW202222830A (zh) | 2022-06-16 |
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