KR20200090889A - Cdkl5 발현 변이체 및 cdkl5 융합 단백질 - Google Patents
Cdkl5 발현 변이체 및 cdkl5 융합 단백질 Download PDFInfo
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- 229960000604 valproic acid Drugs 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
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Abstract
Description
도 1b 및 도 1c는 합성된 CDKL5 작제물 변이체를 도시한 그래프를 나타내고(도 1b), 범례는 작제물이 어떻게 합성되었는지를 설명하기 위해 관련 아미노산 결실 정보와 함께 폴리펩티드의 길이를 기술한다(도 1c).
도 2a 내지 도 2ad는 CHO 세포 또는 대장균 세포와 같은 세포에서 다양한 융합 단백질을 발현하기 위한 예시적인 플라스미드를 나타낸다.
Claims (44)
- CDKL5 폴리펩티드로서, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11 또는 SEQ ID NO: 12에 대해 적어도 98%의 서열 동일성을 갖는 서열을 포함하는, CDKL5 폴리펩티드.
- 제1항에 있어서, 상기 CDKL5 폴리펩티드는 SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11 또는 SEQ ID NO: 12에 대해 적어도 99%의 서열 동일성을 갖는 서열을 포함하는, CDKL5 폴리펩티드.
- 제1항에 있어서, 상기 CDKL5 폴리펩티드는 SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11 또는 SEQ ID NO: 12에 대해 100%의 서열 동일성을 갖는 서열을 포함하는, CDKL5 폴리펩티드.
- 핵 배출 신호(NES)를 결여한 CDKL5 폴리펩티드.
- 제4항에 있어서, 상기 CDKL5 폴리펩티드는 핵 위치 신호(NLS)를 함유하는, CDKL5 폴리펩티드.
- 제4항에 있어서, 상기 CDKL5 폴리펩티드는 핵 위치 신호(NLS)를 함유하지 않는, CDKL5 폴리펩티드.
- 핵 위치 신호(NLS)를 결여하며 핵 배출 신호(NES)를 함유하는, CDKL5 폴리펩티드.
- 제1항 내지 제7항 중 어느 한 항의 CDKL5 폴리펩티드 및 상기 CDKL5 폴리펩티드에 작동적으로 연결된 리더 신호 폴리펩티드를 포함하는, 융합 단백질.
- 제1항 내지 제7항 중 어느 한 항의 CDKL5 폴리펩티드 및 상기 CDKL5 폴리펩티드에 작동적으로 연결된 세포-침투 폴리펩티드를 포함하는, 융합 단백질.
- 제9항에 있어서, 상기 세포-침투 폴리펩티드는 SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18 또는 SEQ ID NO: 50에 대해 적어도 90%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제9항에 있어서, 상기 세포-침투 폴리펩티드는 SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18 또는 SEQ ID NO: 50에 대해 100%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제9항 내지 제11항 중 어느 한 항에 있어서, 제9항 내지 제11항 중 어느 한 항의 융합 단백질에 작동적으로 연결된 리더 신호 폴리펩티드를 추가로 포함하는, 융합 단백질.
- 제8항 또는 제12항에 있어서, 상기 리더 신호 폴리펩티드는 SEQ ID NO: 48, SEQ ID NO: 49, SEQ ID NO: 51, SEQ ID NO: 52 또는 SEQ ID NO: 53에 대해 적어도 90%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제8항 또는 제12항에 있어서, 상기 리더 신호 폴리펩티드는 SEQ ID NO: 48, SEQ ID NO: 49, SEQ ID NO: 51, SEQ ID NO: 52 또는 SEQ ID NO: 53에 대해 100%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제1항 내지 제7항 중 어느 한 항의 CDKL5 폴리펩티드 또는 제8항 내지 제14항 중 어느 한 항의 융합 단백질; 및
약학적으로 허용되는 담체를 포함하는, 약학 제형. - 제15항의 제형을 이를 필요로 하는 환자에게 투여하는 단계를 포함하는, CDKL5-매개 신경계 장애의 치료 방법.
- 제16항에 있어서, 상기 제형은 척수강내, 정맥내, 수조내, 뇌실내 또는 실질내 투여되는, 방법.
- 제16항 또는 제17항에 있어서, 상기 제형은 척수강내 또는 정맥내 투여되는, 방법.
- 제16항 내지 제18항 중 어느 한 항에 있어서, 상기 CDKL5-매개 신경계 장애는 CDKL5 결핍, 또는 CDKL5 돌연변이 또는 결핍에 의해 야기된 비정형 레트 증후군(Rett Syndrome) 중 하나 이상인, 방법.
- 제1항 내지 제7항 중 어느 한 항의 CDKL5 폴리펩티드 또는 제8항 내지 제14항 중 어느 한 항의 융합 단백질을 제조하는 방법으로서,
상기 CDKL5 폴리펩티드 또는 상기 융합 단백질을 발현시키는 단계; 및
상기 CDKL5 폴리펩티드 또는 상기 융합 단백질을 정제하는 단계를 포함하는, 방법. - 제20항에 있어서, 상기 CDKL5 폴리펩티드 또는 상기 융합 단백질은 차이니즈 햄스터 난소(CHO) 세포, HeLa 세포, 인간 배아 신장(HEK) 세포 또는 대장균 세포에서 발현되는, 방법.
- 제1항 내지 제7항 중 어느 한 항의 CDKL5 폴리펩티드 또는 제8항 내지 제14항 중 어느 한 항의 융합 단백질을 인코딩하는, 폴리뉴클레오티드.
- 제22항의 폴리뉴클레오티드를 포함하는 벡터.
- CDKL5 폴리펩티드 및 함께 작동적으로 연결된 세포-침투 폴리펩티드를 포함하는 융합 단백질로서, 상기 CDKL5 폴리펩티드는 SEQ ID NO: 1 또는 SEQ ID NO: 47에 대해 적어도 98%의 서열 동일성을 갖는 서열을 포함하고, 상기 세포-침투 폴리펩티드는 SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 18 또는 SEQ ID NO: 50에 대해 적어도 90%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제24항에 있어서, 상기 세포-침투 폴리펩티드는 SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 18 또는 SEQ ID NO: 50에 대해 적어도 95%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제25항에 있어서, 상기 세포-침투 폴리펩티드는 SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 18 또는 SEQ ID NO: 50에 대해 100%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제24항 내지 제26항 중 어느 한 항에 있어서, 리더 신호 폴리펩티드를 추가로 포함하는, 융합 단백질.
- 제27항에 있어서, 상기 리더 신호 폴리펩티드는 SEQ ID NO: 48, SEQ ID NO: 49, SEQ ID NO: 51, SEQ ID NO: 52 또는 SEQ ID NO: 53에 대해 적어도 90%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제28항에 있어서, 상기 리더 신호 폴리펩티드는 SEQ ID NO: 48, SEQ ID NO: 49, SEQ ID NO: 51, SEQ ID NO: 52 또는 SEQ ID NO: 53에 대해 100%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- CDKL5 폴리펩티드 및 함께 작동적으로 연결된 리더 신호 폴리펩티드를 포함하는 융합 단백질로서, 상기 CDKL5 폴리펩티드는 SEQ ID NO: 1 또는 SEQ ID NO: 47에 대해 적어도 98%의 서열 동일성을 갖는 서열을 포함하고, 상기 리더 신호 폴리펩티드는 SEQ ID NO: 48, SEQ ID NO: 51, SEQ ID NO: 52 또는 SEQ ID NO: 53에 대해 적어도 90%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제30항에 있어서, 상기 리더 신호 폴리펩티드는 SEQ ID NO: 48, SEQ ID NO: 51, SEQ ID NO: 52 또는 SEQ ID NO: 53에 대해 100%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제30항 또는 제31항에 있어서, 세포-침투 폴리펩티드를 추가로 포함하는, 융합 단백질.
- 제32항에 있어서, 상기 세포-침투 폴리펩티드는 SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18 또는 SEQ ID NO: 50에 대해 적어도 90%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제33항에 있어서, 상기 세포-침투 폴리펩티드는 SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18 또는 SEQ ID NO: 50에 대해 적어도 95%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제34항에 있어서, 상기 세포-침투 폴리펩티드는 SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18 또는 SEQ ID NO: 50에 대해 100%의 서열 동일성을 갖는 서열을 포함하는, 융합 단백질.
- 제24항 내지 제35항 중 어느 한 항의 융합 단백질; 및 약학적으로 허용되는 담체를 포함하는, 약학 제형.
- 제36항의 제형을 이를 필요로 하는 환자에게 투여하는 단계를 포함하는, CDKL5-매개 신경계 장애의 치료 방법.
- 제37항에 있어서, 상기 제형은 척수강내, 정맥내, 수조내, 뇌실내 또는 실질내 투여되는, 방법.
- 제37항 또는 제38항에 있어서, 상기 제형은 척수강내 또는 정맥내 투여되는, 방법.
- 제37항 내지 제39항 중 어느 한 항에 있어서, 상기 CDKL5-매개 신경계 장애는 CDKL5 결핍, 또는 CDKL5 돌연변이 또는 결핍에 의해 야기된 비정형 레트 증후군 중 하나 이상인, 방법.
- 제24항 내지 제35항 중 어느 한 항에 따른 융합 단백질을 제조하는 방법으로서,
상기 융합 단백질을 발현시키는 단계; 및
상기 융합 단백질을 정제하는 단계를 포함하는, 방법. - 제41항에 있어서, 상기 융합 단백질은 차이니즈 햄스터 난소(CHO) 세포, HeLa 세포, 인간 배아 신장(HEK) 세포 또는 대장균 세포에서 발현되는, 방법.
- 제24항 내지 제35항 중 어느 한 항의 융합 단백질을 인코딩하는 폴리뉴클레오티드.
- 제43항의 폴리뉴클레오티드를 포함하는 벡터.
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| Application Number | Priority Date | Filing Date | Title |
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| US201762592936P | 2017-11-30 | 2017-11-30 | |
| US201762592944P | 2017-11-30 | 2017-11-30 | |
| US62/592,936 | 2017-11-30 | ||
| US62/592,944 | 2017-11-30 | ||
| PCT/US2018/063294 WO2019108924A2 (en) | 2017-11-30 | 2018-11-30 | Cdkl5 expression variants and cdkl5 fusion proteins |
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| US (1) | US20200299654A1 (ko) |
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Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT201900008877A1 (it) * | 2019-06-13 | 2020-12-13 | Univ Bologna Alma Mater Studiorum | Nuovi costrutti per terapia genica |
| US20230043046A1 (en) * | 2019-10-30 | 2023-02-09 | Amicus Therapeutics, Inc. | Recombinant CDKL5 Proteins, Gene Therapy and Production Methods |
| KR20230003569A (ko) * | 2020-04-27 | 2023-01-06 | 더 트러스티스 오브 더 유니버시티 오브 펜실베니아 | Cdkl5 결핍 장애 (cdd)의 치료에 유용한 조성물 |
| CN114304068B (zh) * | 2020-09-30 | 2025-07-18 | 中国科学院脑科学与智能技术卓越创新中心 | 癫痫动物模型的制备及其应用 |
| IL303239A (en) | 2020-12-01 | 2023-07-01 | Univ Pennsylvania | Compositions and their uses for the treatment of Engelmann syndrome |
| CN114716569B (zh) * | 2022-04-13 | 2023-11-10 | 浙江大学 | 一种携带目标蛋白自主进入真核细胞的重组蛋白、重组表达载体和重组菌及应用 |
| CN116377050A (zh) * | 2022-12-16 | 2023-07-04 | 湖南家辉生物技术有限公司 | 一种发育性癫痫性脑病2型致病基因cdkl5突变位点的应用及其检测试剂和应用 |
| WO2025050032A1 (en) * | 2023-08-31 | 2025-03-06 | Ultragenyx Pharmaceutical Inc. | Methods of producing cdkl5 proteins and uses of the same |
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| WO2005072470A2 (en) * | 2004-01-28 | 2005-08-11 | Exelixis, Inc | Mbms as modifiers of branching morphogenesis and methods of use |
| US7510850B2 (en) * | 2005-11-10 | 2009-03-31 | Carnegie Institution Of Washington | Isolation of the mitotic spindle matrix and its methods of use |
| WO2008151388A1 (en) * | 2007-06-15 | 2008-12-18 | Cytomatrix Pty Ltd | Methods of initiating insulin production |
| ES2829199T3 (es) * | 2010-11-22 | 2021-05-31 | Amicus Therapeutics Inc | Nuevas secuencias de señalización para mejorar la expresión y segregación de proteínas de enzimas recombinantes y otras proteínas |
| EP2679677A1 (en) * | 2012-06-29 | 2014-01-01 | Lysando Aktiengesellschaft | Composition for use in Mycobacteria therapy |
| US20150093399A1 (en) * | 2013-08-28 | 2015-04-02 | Bioasis Technologies, Inc. | Cns-targeted conjugates having modified fc regions and methods of use thereof |
| SG10202000537RA (en) * | 2014-02-28 | 2020-03-30 | Univ Bologna Alma Mater Studiorum | Tatk-cdkl5 fusion proteins, compositions, formulations, and use thereof |
| CN104086656A (zh) * | 2014-03-27 | 2014-10-08 | 华东理工大学 | 一种TAT-RhoGDI2融合蛋白及其制备方法和应用 |
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- 2018-11-30 US US16/768,511 patent/US20200299654A1/en not_active Abandoned
- 2018-11-30 AU AU2018375754A patent/AU2018375754A1/en not_active Abandoned
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- 2018-11-30 MX MX2020005670A patent/MX2020005670A/es unknown
- 2018-11-30 KR KR1020207018589A patent/KR20200090889A/ko not_active Ceased
- 2018-11-30 TW TW107142931A patent/TW201927825A/zh unknown
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| EP3717642A2 (en) | 2020-10-07 |
| TW201927825A (zh) | 2019-07-16 |
| AU2018375754A1 (en) | 2020-07-16 |
| WO2019108924A2 (en) | 2019-06-06 |
| CN111936624A (zh) | 2020-11-13 |
| US20200299654A1 (en) | 2020-09-24 |
| CA3083951A1 (en) | 2019-06-06 |
| JP2021505135A (ja) | 2021-02-18 |
| MX2020005670A (es) | 2020-11-24 |
| WO2019108924A3 (en) | 2019-08-15 |
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