Invention Grant
US07811771B2 Method for the functional determination of mannan-binding-lectin associated serine proteases (MASPs) and complexes thereof
有权
甘露聚糖结合凝集素相关丝氨酸蛋白酶(MASP)及其复合物的功能测定方法
- Patent Title: Method for the functional determination of mannan-binding-lectin associated serine proteases (MASPs) and complexes thereof
- Patent Title (中): 甘露聚糖结合凝集素相关丝氨酸蛋白酶(MASP)及其复合物的功能测定方法
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Application No.: US11793851Application Date: 2005-12-19
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Publication No.: US07811771B2Publication Date: 2010-10-12
- Inventor: Johan Hendrikus Verheijen , Jan Roeland Occo Hanemaaijer , Natascha Alexandra Van Lent , Johannes Hendrikus Nicolaas Lindeman , Mohamed Rahoef Daha , Johanna Roos
- Applicant: Johan Hendrikus Verheijen , Jan Roeland Occo Hanemaaijer , Natascha Alexandra Van Lent , Johannes Hendrikus Nicolaas Lindeman , Mohamed Rahoef Daha , Johanna Roos
- Applicant Address: NL Delft
- Assignee: Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO
- Current Assignee: Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO
- Current Assignee Address: NL Delft
- Agency: Weingarten, Schurgin, Gagnebin & Lebovici LLP
- Priority: EP04078507 20041223
- International Application: PCT/NL2005/000874 WO 20051219
- International Announcement: WO2006/068469 WO 20060629
- Main IPC: G01N33/53
- IPC: G01N33/53

Abstract:
This invention relates to the field of determining, assaying or quantifying activity of components of the complement system. More particularly, the invention relates to methods for detecting the presence or level of activity in a sample of mannan-binding-lectin associated serine proteases (MASPs) or complexes of such proteases with lectins and to detection of the particular lectins themselves. Provided is a method for determining the activity of a MASP in a sample, comprising incubating the sample with a pro-urokinase comprising at its activation site the consensus sequence Arg/Leu/Gly-Yyy-Arg/Lys-Ile/Leu/Val-Zzz-Gly-Gly cleavable by a MASP, wherein Yyy can be any amino acid and Zzz is preferably an aliphatic amino acid, and determining proteolytic activation of said pro-urokinase.
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