KR20200035115A - 입체형태적으로 안정화된 rsv 융합전 f 단백질 - Google Patents
입체형태적으로 안정화된 rsv 융합전 f 단백질 Download PDFInfo
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Abstract
Description
도 2. 198Y-226Y DT 가교 결합("디자인 1") 및 185Y-428Y DT 가교 결합(디자인 2)를 포함하는 돌연변이 RSV F 분자의 개략도. 항원 부위 Ø, IV, 및 V가 분자의 구조와 관련하여 표시되어 있다.
도 3a 내지 도 3b. 도 3a - DT 가교결합 반응을 수행한 후, 198Y와 226Y 사이의 분자내 가교결합("디자인 1")에 의해 도입된 안정성을, 부위 Ø에 결합하는 융합전-특이적 mAb인 D25를 사용하여 ELISA에 의해 2주에 걸쳐 4℃에서 측정하였다. 도 3b - 185Y와 428Y 사이의 분자간 DT 결합 형성("디자인 2")을, WT(모타비주맙(Motavizumab)이 1차 Ab임)와 비교함으로써, 웨스턴 블롯팅에 의해 검정하였다. F1 단백질은 삼량체(TM)의 크기로 이동한다.
도 4. DT-가교결합된 AVR02의 생성을 위한 예시적인 프로토콜의 개략도.
도 5a 내지 도 5b. 정규화를 위해 모타비주맙을 사용하고, 입체형태 완전성을 평가하기 위해 항원 부위 IV/V에 결합하는 항체(도 5a) 및 부위 Ø에 결합하는 항체(도 5b)를 사용한, ELISA에 의한 428Y RSV F 돌연변이체(AVR02)의 가교결합되지 않은 버전인 DS-Cav1과, 428Y 돌연변이체의 DT 가교결합된 버전(DT-AVR02)의 입체형태 완전성의 비교.
도 6a 내지 도 6c. 100시간 37℃ 열-공격 후의 부위 Ø 항원성. 도 6a. 4℃ 및 37℃에서 인큐베이션 후 428Y RSV F 돌연변이체(AVR02) 및 428Y RSV F 돌연변이체의 DT 가교결합된 버전(DT-AVR02)으로의 5C4(부위 Ø)의 결합의 유지 비교. 도 6b. 37℃에서 100시간 인큐베이션 후의 DS-Cav1 및 DT-AVR02으로의 5C4 및 D25 결합 유지. 각 쌍의 왼쪽 막대는 5C4이다. 각 쌍의 오른쪽 막대는 D25이다. 도 6c. 4℃에서 5 주 후의 428Y RSV F 돌연변이체(AVR02)로의 5C4(부위 Ø)의 결합 유지.
도 7. 마우스 생체내에서의 DT 가교결합된 428Y RSV F 돌연변이체(DT-AVR02 또는 DT-preF)의 효능. 중화 역가. 명반 상의 DSCAV1 또는 DT-AVR02로 백신접종된 동물로부터의 RSV-RenillaLuc 중화 역가.
도 8. 예시적인 백신접종 일정의 개략도.
도 9. 코튼 래트 생체내에서의 DT 가교결합된 428Y RSV F 돌연변이체(DT-AVR02 또는 DT-preF로 지칭됨)의 효능. +39일째의 코 세척액 중의 RSV/A/트레이시(Tracy) 역가에 미치는 Alhydrogel 2%로 애쥬번트 처리된 DT 가교결합된 428Y RSV F 돌연변이체의 영향. RSV 역가는 표시된 대조표준 및 처리 그룹 각각에 대해 도시되어 있다.
도 10. 코튼 래트 생체내에서의 DT 가교결합된 428Y RSV F 돌연변이체(DT-AVR02/DT-preF)의 효능. +39일째의 폐 세척액 중의 RSV/A/트레이시 역가에 대한 Alhydrogel 2%로 애쥬번트 처리된 DT 가교결합된 428Y RSV F 돌연변이체. RSV 역가는 표시된 대조표준 및 처리 그룹 각각에 대해 도시되어 있다.
도 11. 코튼 래트 생체내에서의 DT 가교결합된 428Y RSV F 돌연변이체(DT-AVR02/DT-preF)의 효능. RSV/A/트레이시 혈청 중화 항체의 생성에 미치는 Alhydrogel 2%로 애쥬번트 처리된 DT-preF의 영향.
도 12. 코튼 래트 생체내에서의 DT 가교결합된 428Y RSV F 돌연변이체(DT-AVR02/DT-preF)의 효능. RSV/B/1853 교차-반응 중화 항체의 생성에 미치는 Alhydrogel 2%로 애쥬번트 처리된 DT-preF의 영향.
도 13a 내지 도 13d. 427(447Y) 대신 위치 428(428Y)에서의 티로신 치환은 RSV F 돌연변이체의 항원 프로파일을 현격하게 개선시킨다. 스트렙탁틴(Streptactin) 정제된 가용성 427Y(DT-Cav1) 돌연변이체(도 13a 내디 도 13b) 또는 428Y(DT-AVR02) 돌연변이체(도 13c 내지 도 13d)를 DT 가교결합시키고, 정제하고, 표시된 mAb를 사용하여 항원성을 분석하였다. ELISA를 모타비주맙을 사용하여 총 단백질에 대해 정규화하고, Ni-NTA 코팅된 플레이트 상에서 수행하였다. DSCav1을 양성 대조표준으로 사용하였다. 융합전 구조를 2개의 입체형태 항체, 즉, 부위 Ø에 특이적인 mAb 및 항원 부위 IV/V 중간에 결합하는 융합전 특이적 mAb로 프로빙(probing)하였다.
도 14a 내지 도 14c. 크기 배제 크로마토그래피(SEC) 및 SDS-PAGE 분석은 DT 가교결합된 427Y RSV F 돌연변이체(DT-Cav1)와 DT 가교결합된 428Y RSV F 돌연변이체(DT-AVR02)의 현저하게 다른 프로파일을 나타낸다. 디-티로신 가교결합 반응 직후의 표시된 RSV F 돌연변이체(상부 좌측에 있는 도 14a의 427Y/DT-Cav1 및 하부 좌측에 있는 도 14b의 428Y/DT-AVR02)의 크기 배제 크로마토그래피 프로파일이 도시되어 있다. 428Y 돌연변이는 가교결합 반응 후 고차 종(higher-order species)의 현격한 감소를 달성한다. SDS-PAGE 겔 상에서 환원 및 변성 조건 하에서 분리하고, 이어서 쿠마시(Coomassie) 염색한 후의 최종 생성물이 도 14c에 도시되어 있다(우측). 화살표는 고차 종(427Y/DT-Cav1) 및 가교결합된 삼량체 종(428Y/DT-AVR02)을 나타낸다.
도 15a 내지 도 15b. DT 가교결합된 428Y RSV F 돌연변이체(DT-AVR02)로 백신접종된 동물의 혈청 중화 역가는 DT 가교결합된 427Y RSV F 돌연변이체(DT-Cav1)로 백신접종된 동물의 혈청 중화 역가보다 현격하게 높다. 동물을 10 ug(마이크로그램)의 DS-Cav1 대조표준(벤치마크(benchmark) 비교물질) 또는 표시된 DT 가교결합된 분자(도 15a의 427Y/DT-Cav1(좌측) 및 도 15b의 428Y/DT-AVR02(우측))로 프라임-부스트 요법으로 백신접종하였다. 부스트 후 혈청을 채취하고, 열-비활성화시키고, RSV-레닐라(Renilla) 루시퍼라제 리포터 바이러스를 사용하여 중화 역가를 수득하였다. 표시된 바와 같은 중화 역가는 그룹당 5마리 동물의 평균이며, 루시퍼라제 활성의 50% 억제를 가져오는 혈청 희석률의 역수로서 계산된다.
도 16a 내지 도 16b. 수크로스를 사용한 제형화는 RSV F 응집체의 형성을 감소시킨다. DT-가교결합된 428Y 돌연변이체(DT-AVR02)를 사용하여 실험을 수행하였다. 최종 농축 후, 분석용 크기-배제 크로마토그래피(SEC)를 수행하였다. 도 16a에 도시된 바와 같이, 3개의 피크가 확인되었고,이 중 피크 C는 삼량체이고, 피크 A 및 B는 응집체이다. 정제 단계의 용리 동안 10% 수크로스를 사용한 DT-AVR02 분자의 제형화는 응집체의 형성을 제거하는 것으로 나타났다. 도 16b에 도시된 바와 같이, 10% 수크로스를 사용하여 제형화된 샘플에서 피크 C(삼량체)는 남아 있었지만 피크 A 및 B(응집체)는 명백하지 않았다.
Claims (65)
- 아미노산 잔기 428, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 잔기 428에 상응하는 아미노산에서의 티로신으로의 점 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제1항에 있어서, 아미노산 잔기 185, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 잔기 185에 상응하는 아미노산에서의 티로신으로의 점 돌연변이를 추가로 포함하는, 돌연변이 RSV F 분자.
- 제1항에 있어서, 아미노산 잔기 226, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 잔기 226에 상응하는 아미노산에서의 티로신으로의 점 돌연변이를 추가로 포함하는, 돌연변이 RSV F 분자.
- 제1항에 있어서, (a) 아미노산 잔기 185, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 잔기 185에 상응하는 아미노산에서의 티로신으로의 점 돌연변이, 및 (b) 아미노산 잔기 226, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 잔기 226에 상응하는 아미노산에서의 티로신으로의 점 돌연변이를 추가로 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제4항 중 어느 한 항에 있어서, 막관통 도메인 및 세포질 도메인을 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제4항 중 어느 한 항에 있어서, 상기 분자는 막관통 도메인 또는 세포질 도메인을 포함하지 않는, 돌연변이 RSV F 분자.
- 제1항 내지 제6항 중 어느 한 항에 있어서, 상기 분자는 RSV 타입 A 또는 RSV 타입 B 분자인, 돌연변이 RSV F 분자.
- 제1항 내지 제7항 중 어느 한 항에 있어서, 상기 분자는 융합전 특이적 항체에 결합하는, 돌연변이 RSV F 분자.
- 제1항 내지 제8항 중 어느 한 항에 있어서, 상기 분자는 항원 부위 Ø를 인식하는 항체에 결합하는, 돌연변이 RSV F 분자.
- 제1항 내지 제9항 중 어느 한 항에 있어서, 상기 분자는 D25, 5C4, AM22 및 AM14로 이루어진 군으로부터 선택된 항체에 결합하는, 돌연변이 RSV F 분자.
- 제1항 내지 제10항 중 어느 한 항에 있어서, 상기 분자는 F2 폴리펩티드 및 F1 폴리펩티드를 포함하고, 상기 F2 폴리펩티드의 C-말단은 이황화물 결합에 의해 상기 F1 폴리펩티드의 N-말단에 연결되는, 돌연변이 RSV F 분자.
- 제1항 내지 제11항 중 어느 한 항에 있어서, 상기 분자는 F2 폴리펩티드 및 F1 폴리펩티드를 포함하고, 상기 F2 폴리펩티드의 C-말단은 인공적으로 도입된 펩티드 링커에 의해 상기 F1 폴리펩티드의 N-말단에 연결되는, 돌연변이 RSV F 분자.
- 제1항 내지 제12항 중 어느 한 항에 있어서, 대략 84개 아미노산 잔기의 F2 폴리펩티드 및 대략 375개 아미노산 잔기의 F1 폴리펩티드를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제13항 중 어느 한 항에 있어서, 대략 74개 내지 84개 아미노산 잔기의 F2 폴리펩티드 및 대략 365개 내지 375개 아미노산 잔기의 F1 폴리펩티드를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제14항 중 어느 한 항에 있어서, (a) SEQ ID NO. 21 내지 SEQ ID NO. 81 중 어느 하나의 아미노산 잔기 26-109를 포함하거나 이로 이루어진 F2 폴리펩티드, 및 (b) SEQ ID NO. 21 내지 SEQ ID NO. 81 중 어느 하나의 아미노산 잔기 137-513을 포함하거나 이로 이루어진 F1 폴리펩티드를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제15항 중 어느 한 항에 있어서, (a) SEQ ID NO. 21 내지 SEQ ID NO. 81 중 어느 하나의 아미노산 잔기 26-109로부터의 대략 74개 내지 84개의 아미노산을 포함하거나 이로 이루어진 F2 폴리펩티드, 및 (b) SEQ ID NO. 21 내지 SEQ ID NO. 81 중 어느 하나의 아미노산 잔기 137-513으로부터의 대략 365개 내지 375개의 아미노산을 포함하거나 이로 이루어진 F1 폴리펩티드를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제16항 중 어느 한 항에 있어서, (a) SEQ ID NO. 81의 아미노산 잔기 26-109를 포함하거나 이로 이루어진 F2 폴리펩티드, 및 (b) SEQ ID NO. 81의 아미노산 잔기 137-513을 포함하거나 이로 이루어진 F1 폴리펩티드를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제17항 중 어느 한 항에 있어서, (a) SEQ ID NO. 81의 아미노산 잔기 26-109 중 대략 74개 내지 84개의 아미노산을 포함하거나 이로 이루어진 F2 폴리펩티드, 및 (b) SEQ ID NO. 81의 아미노산 잔기 137-513 중 대략 365개 내지 375개의 아미노산을 포함하거나 이로 이루어진 F1 폴리펩티드를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제18항 중 어느 한 항에 있어서, 상기 분자는 하나 이상의 디-티로신 가교 결합에 의해 융합전 입체형태로 안정화되는, 돌연변이 RSV F 분자.
- 제1항 내지 제19항 중 어느 한 항에 있어서, 상기 분자는 성숙 RSV F 삼량체인, 돌연변이 RSV F 분자.
- 제1항 내지 제20항 중 어느 한 항에 있어서, 상기 분자는 3개 이상의 디-티로신 가교 결합에 의해 융합전 입체형태로 안정화된 성숙 RSV F 삼량체인, 돌연변이 RSV F 분자.
- 제1항 내지 제21항 중 어느 한 항에 있어서, 상기 분자는 (a) 아미노산 잔기 428, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신, 및 (b) 아미노산 잔기 185, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신 사이의 디-티로신 가교 결합을 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제22항 중 어느 한 항에 있어서, 상기 분자는 (a) 아미노산 잔기 198, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신, 및 (b) 아미노산 잔기 226, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신 사이의 디-티로신 가교 결합을 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제23항 중 어느 한 항에 있어서, 상기 분자는 (i) 아미노산 잔기 198 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신과, 아미노산 잔기 226 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신 사이의 디-티로신 가교 결합, 및 (ii) 아미노산 잔기 428 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신과, 아미노산 잔기 185 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신 사이의 디-티로신 가교 결합 모두를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제24항 중 어느 한 항에 있어서, 상기 분자는 3개의 디-티로신 가교 결합 - 이들 각각은 (a) 아미노산 잔기 428, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신과, (b) 아미노산 잔기 185, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신 사이에 존재함 -을 포함하는 성숙 RSV F 삼량체인, 돌연변이 RSV F 분자.
- 제1항 내지 제25항 중 어느 한 항에 있어서, 상기 분자는 3개의 디-티로신 가교 결합 - 이들 각각은 (a) 아미노산 잔기 198, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신과, (b) 아미노산 잔기 226, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신 사이에 존재함 -을 포함하는 성숙 RSV F 삼량체인, 돌연변이 RSV F 분자.
- 제1항 내지 제26항 중 어느 한 항에 있어서, 상기 분자는 6개의 디-티로신 가교 결합을 포함하는 성숙 RSV F 삼량체이며, 상기 6개의 디-티로신 가교 결합 중 (i) 3개는 아미노산 잔기 198, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신과, 아미노산 잔기 226, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신 사이에 존재하고, (ii) 3개는 아미노산 잔기 428, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신과, 아미노산 잔기 185, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에 있는 티로신 사이에 존재하는, 돌연변이 RSV F 분자.
- 제1항 내지 제27항 중 어느 한 항에 있어서, 상기 분자는 하나 이상의 인공적으로 도입된 비-DT 가교 결합을 추가로 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제28항 중 어느 한 항에 있어서, 상기 분자는 하나 이상의 인공적으로 도입된 이황화물 결합을 추가로 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제29항 중 어느 한 항에 있어서, 상기 분자는 하나 이상의 시스테인으로의 점 돌연변이를 추가로 포함하는, 돌연변이 RSV F 분자.
- 제29항에 있어서, 상기 이황화물 결합은 2개의 시스테인 - 이들 중 하나 또는 둘 모두는 점 돌연변이에 의해 도입됨 - 사이에 형성되는, 돌연변이 RSV F 분자.
- 제1항 내지 제31항 중 어느 한 항에 있어서, 상기 분자는 아미노산 잔기 155, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 시스테인으로의 점 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제32항 중 어느 한 항에 있어서, 상기 분자는 아미노산 잔기 290, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 시스테인으로의 점 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제33항 중 어느 한 항에 있어서, 상기 분자는 (a) 아미노산 잔기 155, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 시스테인으로의 점 돌연변이, 및 (b) 아미노산 잔기 290, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 시스테인으로의 점 돌연변이 모두를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제34항 중 어느 한 항에 있어서, 상기 분자는 하나 이상의 인공적으로 도입된 빈 곳-채움(cavity-filling) 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제35항에 있어서, 상기 분자는 아미노산 잔기 190, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 페닐알라닌으로의 점 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제35항에 있어서, 상기 분자는 아미노산 잔기 207, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 류신으로의 점 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제35항에 있어서, 상기 분자는 (a) 아미노산 잔기 190, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 페닐알라닌으로의 점 돌연변이, 및 (b) 아미노산 잔기 207, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 류신으로의 점 돌연변이 모두를 포함하는, 돌연변이 RSV F 분자.
- 제35항에 있어서, 상기 분자는 58W, 83W, 87F, 90L, 153W, 190F, 203W, 207L, 220L, 260W, 296F, 및 298L로 이루어진 군으로부터 선택된 하나 이상의 빈 곳-채움 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제39항 중 어느 한 항에 있어서, 상기 분자는 이종성 올리고머화 도메인을 포함하는, 돌연변이 RSV F 분자.
- 제40항에 있어서, 상기 이종성 올리고머화 도메인은 삼량체화 도메인인, 돌연변이 RSV F 분자.
- 제41항에 있어서, 상기 삼량체화 도메인은 폴돈(foldon) 도메인, GCN4 도메인, 또는 T4 피브리니틴 도메인인, 돌연변이 RSV F 분자.
- 제41항에 있어서, 상기 삼량체화 도메인은 SEQ ID NO. 93을 포함하는 폴돈 도메인인, 돌연변이 RSV F 분자.
- 제1항 내지 제43항 중 어느 한 항에 있어서, 상기 분자는 상기 RSV F 분자의 검출에 유용한 하나 이상의 태그를 포함하는, 돌연변이 RSV F 분자.
- 제1항 내지 제44항 중 어느 한 항에 있어서, 상기 분자는 상기 RSV F 분자의 정제에 유용한 하나 이상의 태그를 포함하는, 돌연변이 RSV F 분자.
- 제44항 또는 제45항에 있어서, 상기 태그는 Strep 태그, Strep II 태그, FLAG 태그, 글루타티온 S-트랜스퍼라제(GST) 태그, 녹색 형광 단백질(GFP) 태그, 헤마글루티닌 A(HA) 태그, 히스티딘(His) 태그, 루시퍼라제 태그, 말토스-결합 단백질(MBP) 태그, c-Myc 태그, 단백질 A 태그, 및 단백질 G 태그로 이루어진 군으로부터 선택되는, 돌연변이 RSV F 분자.
- 제44항 또는 제45항에 있어서, 상기 태그는 SEQ ID NO. 95를 포함하는, 돌연변이 RSV F 분자.
- 제44항 또는 제45항에 있어서, 상기 태그는 SEQ ID NO. 96을 포함하는, 돌연변이 RSV F 분자.
- 제44항 내지 제48항 중 어느 한 항에 있어서, 상기 태그는 단백질분해적으로 절단 가능한 태그인, 돌연변이 RSV F 분자.
- (a) 아미노산 잔기 428, (b) 아미노산 잔기 226, 및 (c) 아미노산 잔기 185, 또는 SEQ ID NO.1에 대한 정렬에 의해 결정된 바와 같은 이들 중 어느 하나에 상응하는 아미노산 각각에서의 티로신으로의 점 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제50항에 있어서, SEQ ID NO. 81의 아미노산 잔기 26-109 및 아미노산 잔기 137-513을 포함하는, 돌연변이 RSV F 분자.
- (i) (a) 아미노산 잔기 428, (b) 아미노산 잔기 226, 및 (c) 아미노산 잔기 185, 또는 SEQ ID NO.1에 대한 정렬에 의해 결정된 바와 같은 이들 중 어느 하나에 상응하는 아미노산 각각에서의 티로신으로의 점 돌연변이, (ii) 아미노산 잔기 190, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 페닐알라닌으로의 점 돌연변이, 및 (iii) 아미노산 잔기 207, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 류신으로의 점 돌연변이를 포함하는, 돌연변이 RSV F 분자.
- 제52항에 있어서, SEQ ID NO. 81의 아미노산 잔기 26-109 및 아미노산 잔기 137-513을 포함하는, 돌연변이 RSV F 분자.
- (a) 아미노산 잔기 428, (b) 아미노산 잔기 226, 및 (c) 아미노산 잔기 185, 또는 SEQ ID NO.1에 대한 정렬에 의해 결정된 바와 같은 이들 중 어느 하나에 상응하는 아미노산 각각에서의 티로신으로의 점 돌연변이를 포함하는, 가용성 성숙 삼량체 RSV F 분자.
- 제54항에 있어서, SEQ ID NO. 81의 아미노산 잔기 26-109 및 아미노산 잔기 137-513을 포함하는, 가용성 성숙 삼량체 RSV F 분자.
- (i) (a) 아미노산 잔기 428, (b) 아미노산 잔기 226, 및 (c) 아미노산 잔기 185, 또는 SEQ ID NO.1에 대한 정렬에 의해 결정된 바와 같은 이들 중 어느 하나에 상응하는 아미노산 각각에서의 티로신으로의 점 돌연변이, (ii) 아미노산 잔기 190, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 페닐알라닌으로의 점 돌연변이, 및 (iii) 아미노산 잔기 207, 또는 SEQ ID NO. 1에 대한 정렬에 의해 결정된 바와 같은 이에 상응하는 아미노산 잔기에서의 류신으로의 점 돌연변이를 포함하는, 가용성 성숙 삼량체 RSV F 분자.
- 제56항에 있어서, SEQ ID NO. 81의 아미노산 잔기 26-109 및 아미노산 잔기 137-513을 포함하는, 가용성 성숙 삼량체 RSV F 분자.
- 제50항 내지 제57항 중 어느 한 항에 있어서, 상기 분자는 하나 이상의 DT 가교 결합을 포함하고, pre-F 입체형태로 안정화되는, RSV F 분자.
- 제1항 내지 제58항 중 어느 한 항에 따른 돌연변이 RSV F 분자를 인코딩하는 핵산.
- 제59항에 따른 핵산 분자를 포함하는 벡터.
- 제59항의 핵산 분자를 포함하는 세포.
- 제60항의 벡터를 포함하는 세포.
- 제1항 내지 제58항 중 어느 한 항에 따른 돌연변이 RSV 분자를 포함하는 약학 조성물.
- 제63항에 있어서, 애쥬번트를 추가로 포함하는, 약학 조성물.
- 유효량의 제64항의 약학 조성물을 이를 필요로하는 대상체에게 투여하는 단계를 포함하는, RSV에 대해 백신접종하는 방법.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2023055154A1 (ko) * | 2021-09-29 | 2023-04-06 | 에스케이바이오사이언스 주식회사 | 재조합된 약독화 rsv 생백신 및 이를 제조하는 방법 |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2773309T3 (es) | 2013-07-25 | 2020-07-10 | Calder Biosciences Inc | Proteínas F de pre-fusión de VRS estabilizadas conformacionalmente |
WO2019032480A1 (en) * | 2017-08-07 | 2019-02-14 | Avatar Medical, Llc | PROTEINS F PRE-FUSION OF RSV STABILIZED IN TERMS OF CONFORMATION |
WO2019178521A1 (en) | 2018-03-16 | 2019-09-19 | University Of Pittsburgh-Of The Commonwealth System Of Higher Education | Compositions and methods for vaccination against respiratory syncitial virus infection |
WO2020205986A1 (en) * | 2019-04-02 | 2020-10-08 | Sanofi | Antigenic multimeric respiratory syncytial virus polypeptides |
CN110054668B (zh) * | 2019-04-25 | 2021-09-10 | 北京交通大学 | 一种呼吸道合胞病毒融合前f蛋白及其应用 |
CN112552380B (zh) * | 2020-12-10 | 2021-12-24 | 武汉博沃生物科技有限公司 | 一种SARS-CoV-2病毒的免疫原及其应用 |
WO2022122036A1 (zh) * | 2020-12-10 | 2022-06-16 | 武汉博沃生物科技有限公司 | 一种SARS-CoV-2病毒的免疫原、药物组合物及其应用 |
CN117715923A (zh) * | 2022-04-29 | 2024-03-15 | 北京新合睿恩生物医疗科技有限公司 | Rsv f蛋白突变体及其应用 |
WO2024078597A1 (en) * | 2022-10-13 | 2024-04-18 | Rvac Medicines (Us) , Inc. | Rsv f protein variants and uses thereof |
CN116478296B (zh) * | 2022-10-17 | 2024-02-23 | 厦门大学 | 截短的呼吸道合胞病毒f蛋白及其用途 |
WO2024193380A1 (zh) * | 2023-03-17 | 2024-09-26 | 成都威斯克生物医药有限公司 | 抗呼吸道合胞病毒感染的疫苗 |
CN118930654A (zh) * | 2023-05-12 | 2024-11-12 | 中国科学院微生物研究所 | 一种呼吸道合胞病毒抗原制备方法和应用 |
CN117050149A (zh) * | 2023-05-19 | 2023-11-14 | 珠海丽凡达生物技术有限公司 | 包含人呼吸道合胞病毒抗原的免疫组合物及其制备方法和应用 |
CN117720628A (zh) * | 2023-10-12 | 2024-03-19 | 中国科学院微生物研究所 | 一种呼吸道合胞病毒二价抗原制备方法和应用 |
WO2025092933A1 (zh) * | 2023-10-31 | 2025-05-08 | 上海蓝鹊生物医药有限公司 | 一种rsv抗原、核酸、重组表达载体、药物组合物及其应用 |
CN117304279B (zh) * | 2023-11-28 | 2024-04-16 | 江苏瑞科生物技术股份有限公司 | 一种重组rsv f蛋白及其应用 |
CN117304281B (zh) * | 2023-11-28 | 2024-04-16 | 江苏瑞科生物技术股份有限公司 | 一种重组rsv f蛋白及其应用 |
CN118146321B (zh) * | 2024-03-27 | 2024-08-27 | 普大生物科技(泰州)有限公司 | 一种rsv重组蛋白疫苗及其制备方法 |
CN119305277B (zh) * | 2024-12-13 | 2025-03-18 | 湖南省长城铭泰新材料科技有限公司 | 高阻隔抗菌型软包装材料及其制备方法 |
CN119569836B (zh) * | 2025-02-07 | 2025-07-15 | 复星安特金(成都)生物制药有限公司 | Rsv f蛋白突变体及其应用 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE513056T1 (de) | 1999-10-15 | 2011-07-15 | Avatar Medical L L C | Stabilisierte proteine |
US20050054572A1 (en) | 2003-07-03 | 2005-03-10 | Marshall Christopher P. | Methods for obtaining molecules with reduced immunogenicity |
US20120083008A1 (en) | 2004-07-06 | 2012-04-05 | Marshall Christopher P | Methods for obtaining molecules with reduced immunogenicity |
EP3109258B1 (en) | 2007-12-24 | 2019-01-23 | ID Biomedical Corporation of Quebec | Recombinant rsv antigens |
PL3178490T3 (pl) | 2009-07-15 | 2022-08-01 | Glaxosmithkline Biologicals S.A. | Kompozycje białka f rsv i sposoby ich wytwarzania |
WO2011066221A1 (en) | 2009-11-24 | 2011-06-03 | International Aids Vaccine Initiative | Immunogen prioritization for vaccine design |
US20130236905A1 (en) | 2010-05-18 | 2013-09-12 | Christopher Marshall | Assay for identifying antigens that activate b cell receptors comprising neutralizing antibodies |
SMT201700569T1 (it) | 2011-05-13 | 2018-01-11 | Glaxosmithkline Biologicals Sa | Antigeni f di pre-fusione di rsv |
US20130302366A1 (en) | 2012-05-09 | 2013-11-14 | Christopher Marshall | Conformationally Specific Viral Immunogens |
CA2902877A1 (en) * | 2013-03-13 | 2014-10-02 | Jeffrey Boyington | Prefusion rsv f proteins and their use |
US9738689B2 (en) | 2013-03-13 | 2017-08-22 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Prefusion RSV F proteins and their use |
ES2773309T3 (es) * | 2013-07-25 | 2020-07-10 | Calder Biosciences Inc | Proteínas F de pre-fusión de VRS estabilizadas conformacionalmente |
CA2920016A1 (en) | 2013-08-03 | 2015-02-12 | Avatar Medical, Llc | Influenza hemagglutinin proteins and methods of use thereof |
SG11201804148TA (en) | 2015-12-23 | 2018-07-30 | Pfizer | Rsv f protein mutants |
WO2019032480A1 (en) * | 2017-08-07 | 2019-02-14 | Avatar Medical, Llc | PROTEINS F PRE-FUSION OF RSV STABILIZED IN TERMS OF CONFORMATION |
WO2019178521A1 (en) * | 2018-03-16 | 2019-09-19 | University Of Pittsburgh-Of The Commonwealth System Of Higher Education | Compositions and methods for vaccination against respiratory syncitial virus infection |
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WO2023055154A1 (ko) * | 2021-09-29 | 2023-04-06 | 에스케이바이오사이언스 주식회사 | 재조합된 약독화 rsv 생백신 및 이를 제조하는 방법 |
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