TETRA-FUNCTIONAL CHEMICAL PROBE AND METHOD FOR IDENTIFYING TARGET MEMBRANE PROTEIN FROM LIVING CELL OR LIVING TISSUE BY USING SAID PROBE
This tetra-functional compound is formed by linking, via a spacer as needed, a ligand binding site (A) or a ligand, a reactive site (D), a potential cleavage site (E), and a biotin site (B), wherein: the ligand binding site (A) is an active functional group such as an amine reactive group or a react...
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Zusammenfassung: | This tetra-functional compound is formed by linking, via a spacer as needed, a ligand binding site (A) or a ligand, a reactive site (D), a potential cleavage site (E), and a biotin site (B), wherein: the ligand binding site (A) is an active functional group such as an amine reactive group or a reactive functional group such as -COOH; the reactive site (D) is a group having a structure of a compound such as 2-aryl-5-carboxy-tetrazole; the potential cleavage site (E) is a group having a structure of a compound such as 1-(4 4-dimethyl-2 6-dioxocyclohex-1-ylidene)ethyl; and the spacer is a group obtained by substitution with a cross-linking group such as a linear or branched alkylene group having 1 or more carbon atoms.
一种四官能性化合物,其根据需要通过间隔物连接配体结合性位点(A)或配体、反应性位点(D)、潜在的可切割位点(E)和生物素位点(B)而形成,其中:所述配体结合性位点(A)是活化的官能团例如胺反应性基团或反应性官能团例如-COOH;所述反应性位点(D)是具有化合物例如2-芳基-5-羧基四唑的结构的基团;所述潜在的可切割位点(E)是具有化合物例如1-(4,4-二甲基-2,6-二氧代环己-1-亚基)乙基的结构的基团;并且所述间隔物是通过用交联基团取代获得的基团,例如具有一个或多个碳原子的直链或支链亚烷基。 |
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