JP2002535966A5 - - Google Patents
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- Publication number
- JP2002535966A5 JP2002535966A5 JP2000591070A JP2000591070A JP2002535966A5 JP 2002535966 A5 JP2002535966 A5 JP 2002535966A5 JP 2000591070 A JP2000591070 A JP 2000591070A JP 2000591070 A JP2000591070 A JP 2000591070A JP 2002535966 A5 JP2002535966 A5 JP 2002535966A5
- Authority
- JP
- Japan
- Prior art keywords
- smez
- rspe
- changed
- positions
- smez2
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 108010016626 Dipeptides Proteins 0.000 description 2
- 231100000765 Toxin Toxicity 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003053 toxin Substances 0.000 description 2
- 108020003112 toxins Proteins 0.000 description 2
- 230000001809 detectable Effects 0.000 description 1
- 230000002297 mitogenic Effects 0.000 description 1
- 230000003389 potentiating Effects 0.000 description 1
Images
Description
SMEZとSMEZ−2の間の最も有意な差異は、位置96〜100の交換されたペンタペプチド配列であって、そこではSMEZのEEPMS配列がSMEZ−2ではKTSIPに変えられている(図1)。第2の差異は位置111〜112であり、そこではRRジペプチドがSMEZではGKに変えられている。残りの10個の異なる残基は、ほぼ一次配列全体に広がっている。
SMEZとSMEZ−2の間の最も有意な差異は、位置96〜100のペンタペプチド配列の交換であって、そこではSMEZのEEPMS配列がSMEZ2ではKTSIPに変えられている(図1)。第2のクラスターは位置111〜112であり、RPジペプチドがSMEZ−2ではGKに変えられている。残りの10の異なる残基は一次配列のほぼ全体に広がっている。
rSPE−GおよびrSPE−Hについての1/2最大反応は、それぞれ2pg/mlおよび50pg/mlであった。各々0.02pg/mlおよび0.1pg/ml未満では活性は検出されなかった。したがって双方の毒素は、rSPE−Cよりも効力が低かった。組換えSMEZはrSPE−Cと効力において同様であり、P50%値は0.08pg/mlで、0.5fg/ml未満では検出可能な増殖はなかった。組換えSMEZ−2は、測定されたすべての、あるいは他に述べられた測定可能な限りの毒素よりも強い分裂促進能を示した。 P50%値は0.02pg/mlと測定され、rSMEZ−2は少なくとも0.1fg/ml未満においてもまだ活性があった。すべてのP50%値は表1にまとめられている。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NZ33358998 | 1998-12-24 | ||
NZ333589 | 1998-12-24 | ||
PCT/NZ1999/000228 WO2000039159A1 (en) | 1998-12-24 | 1999-12-24 | Superantigens |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2002535966A JP2002535966A (ja) | 2002-10-29 |
JP2002535966A5 true JP2002535966A5 (ja) | 2006-10-19 |
Family
ID=19927091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000591070A Pending JP2002535966A (ja) | 1998-12-24 | 1999-12-24 | 超抗原 |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1141000A4 (ja) |
JP (1) | JP2002535966A (ja) |
AU (1) | AU764650B2 (ja) |
CA (1) | CA2356755A1 (ja) |
WO (1) | WO2000039159A1 (ja) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ519371A (en) * | 2002-06-04 | 2004-11-26 | Auckland Uniservices Ltd | Immunomodulatory constructs and their uses |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE325617T1 (de) * | 1997-12-02 | 2006-06-15 | Idaho Res Found | Nicht-toxische immun-stimulierende enterotoxin- zusammensetzungen |
-
1999
- 1999-12-24 CA CA002356755A patent/CA2356755A1/en not_active Abandoned
- 1999-12-24 EP EP99962603A patent/EP1141000A4/en not_active Withdrawn
- 1999-12-24 AU AU19010/00A patent/AU764650B2/en not_active Ceased
- 1999-12-24 WO PCT/NZ1999/000228 patent/WO2000039159A1/en active IP Right Grant
- 1999-12-24 JP JP2000591070A patent/JP2002535966A/ja active Pending
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