KR960702522A - 우로키나제 플라스미노겐 활성인자 억제인자의 발현(expression of urokinase plasminogen activator inhibitors) - Google Patents

우로키나제 플라스미노겐 활성인자 억제인자의 발현(expression of urokinase plasminogen activator inhibitors)

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KR960702522A
KR960702522A KR1019950705328A KR19950705328A KR960702522A KR 960702522 A KR960702522 A KR 960702522A KR 1019950705328 A KR1019950705328 A KR 1019950705328A KR 19950705328 A KR19950705328 A KR 19950705328A KR 960702522 A KR960702522 A KR 960702522A
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polypeptide
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plasminogen activator
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로젠버그 스티븐
알.스트라톤-토마스 제니퍼
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로버트 피. 블랙버언
카이론 코퍼레이션
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Abstract

효모로부터 huPA1-48을 발현시킴으로써 우로키나제-타입 플라스미노겐 활성인자 억제인자를 제조하는 방법이 개시되었다.

Description

우로키나제 플라스미노겐 활성인자 억제인자의 발현(EXPRESSION OF UROKINASE PLASMINOGEN ACTIVATOR INHIBITORS)
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (20)

  1. 본질적으로 인간 우로키나제-타입 플라스미노겐 활성인자의 EGF-유사 도메인으로 구성되는 비-푸코실화 폴리펩티드의 제조방법에 있어서, 상기 방법은 본질적으로 인간 우로키나제-타입 플라스미노겐 활성인자의 EGF-유사 도메인으로 구성되는 huPAR 길항제 폴리펩티드 또는 그것의 활성유사체를 코드화하는 올리고뉴클레오티드에 기능적으로 연결된 전사 프로모터를 함유하는 발현 벡터로 형질 전환된 효모숙주를 제공하는 단계; 상기 폴리펩티드의 발현을 촉진하는 조건하에서 상기의 효모숙주를 배양하는 단계; 및 상기 폴리펩티드를 분리하는 단계로 이루어지는 것을 특징으로 하는 방법.
  2. 제1항에 있어서, 상기의 올리고뉴클레오티드는 추가로 상기의 huPAR 길항제 폴리펩티드 또는 유사체에 기능적으로 연결되고, 상기의 숙주세포에서 발현된 폴리펩티드의 분비를 일으키는데 있어 기능적인 시그날 리더 폴리펩티드를 고드화하는 것을 특징으로 하는 방법.
  3. 제2항에 있어서, 상기 시그날 리더는 효모 α-인자 리더로 이루어진 것을 특징으로 하는 방법.
  4. 제3항에 있어서, 상기의 효모 α-인자 리더는 S. cerevisiae α-인자 리더인 것을 특징으로 하는 방법.
  5. 제1항에 있어서, 상기의 숙주세포는 Saccharomyces cerevisiae이 것을 특징으로 하는 방법.
  6. 제1항에 있어서, 상기의 huPAR 길항제 폴리펩티드는 본질적으로 huPA1-48로 구성된 것을 특징으로 하는 방법.
  7. 본질적으로 인간 우로키나제-타입 플라스미노젠 활성인자의 EGF-유사 도메인으로 구성된 비-푸코실화 폴리펩티드 또는 그것의 활성유사체로 이루어진 것을 특징으로 하는 huPAR 길항제 폴리펩티드 조성물.
  8. 제7항에 있어서, 상기의 비-푸코실화 폴리펩티드는 본질적으로 huPAl-48로 구성된 것을 특징으로 하는 조성물.
  9. 제7항에 있어서, 추가로 제약학적으로 허용가능한 부형제를 함유하는 것을 특징으로 하는 조성물.
  10. uPA-매개 장애를 치료하는 방법에 있어서, 상기 방법은 본질적으로 인간 우로키나제-타입 플라스미노겐 활성인자의 EGF-유사 도메인으로 구성되는 비-푸코실화 폴리펩티드 또는 그것의 활성유사체를 이루어진 조성물을 제공하고, 상기 조성물의 유효량을 uPA-매개 장애를 갖는 환자에게 투여하는 것으로 이루어진 것을 특징으로 하는 방법.
  11. 제10항에 있어서, 상기 폴리펩티드는 본질적으로 huPA1-48로 구성된 것을 특징으로 하는 방법.
  12. 제10항에 있어서, 상기의 uPA-매개 장애는 전이, 부적절한 맥관형성, 만성염증으로 구성되는 군으로부터 선택되는 것을 특징으로 하는 방법.
  13. 제12항에 있어서, 상기의 uPA-매개 장애는 카포시 육종, 당뇨명 망막병중, 류머티양 관절염으로 구성되는 군으로부터 선택되는 것을 특징으로 하는 방법.
  14. 제10항에 있어서, 상기 조성물은 눈에의 점적에 의해 투여되는 것을 특징으로 하는 방법.
  15. 표적과의 결합에 대한 스크리닝전에 일가 파지 디스플레이 혼합물을 예비-농화시키는 방법에 있어서, (a) 일가 디스플레이파지와 비-디스플레이파지의 혼합물을 제공하는 단계, 여기서 상기의 일가 디스플레이파지는 후보펩티드와 공통펩티드를 디스플레이하고, 상기 공통펩티드는 각 일가 디스플레이파지에서 동일하고, 상기 후보펩티드는 다른 일가 디스플레이파지에서 다르다; 및 (b) 공통 펩티드를 디스플레이하는 모든 파지를 공통펩티드를 디스플레이하지 않는 파지로부터 분리하는 단계로 이루어지는 것을 특징으로 하는 방법.
  16. 제15항에 있어서, 상기 후보펩티드는 huPA1-48 또는 그것의 활성유사체 또는 활성부분인 것을 특징으로 하는 방법.
  17. 제15항에 있어서, 상기의 공통펩티드는 항체 에피트프로 이루어진 것을 특징으로 하는 방법.
  18. 제17항에 있어서, 상기의 에피토프는 Glu-Tyr-Met-Pro-Met-Glu로 이루어진 것을 특징으로 하는 방법.
  19. 제15항에 있어서, 추가로 (c) 상기의 공통펩티드를 디스플레이하는 상기의 분리된 파지를 상기 표적과 접촉시키는 단계; 및 (d) 상기 표척에 결합한 파지를 상기 표적에 결합하지 않는 파지로부터 분리하는 단계를 더 포함하는 것을 특징으로 하는 방법.
  20. 제19항에 있어서, 상기 표척은 huPAR로 이루어진 것을 특징으로 하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019950705328A 1993-06-01 1994-05-19 우로키나제 플라스미노겐 활성인자 억제인자의 발현(expression of urokinase plasminogen activator inhibitors) KR960702522A (ko)

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US7015393A 1993-06-01 1993-06-01
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PCT/US1994/005669 WO1994028145A2 (en) 1993-06-01 1994-05-19 Expression of urokinase plasminogen activator inhibitors

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US6268341B1 (en) 2001-07-31
ATE239085T1 (de) 2003-05-15
JPH08508172A (ja) 1996-09-03
AU7137994A (en) 1994-12-20
NO954778D0 (no) 1995-11-24
FI955721A (fi) 1995-11-27
CA2162855A1 (en) 1994-12-08
DE69432608D1 (de) 2003-06-12
EP0802983A2 (en) 1997-10-29
NZ268470A (en) 1997-09-22
FI955721A0 (fi) 1995-11-27
WO1994028145A2 (en) 1994-12-08
WO1994028145A3 (en) 1995-10-19
EP0802983B1 (en) 2003-05-02
DE69432608T2 (de) 2004-02-26

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