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光交联剂-聚合物介导的单克隆抗体、F(ab')2和F(ab')片段的固定化。

Photolinker-polymer-mediated immobilization of monoclonal antibodies, F(ab')2 and F(ab') fragments.

作者信息

Gao H, Kislig E, Oranth N, Sigrist H

机构信息

Institute of Biochemistry, University of Bern, Switzerland.

出版信息

Biotechnol Appl Biochem. 1994 Oct;20(2):251-63.

PMID:7986381
Abstract

Photolinker-polymer-mediated covalent immobilization of antibodies, F(ab') and F(ab')2 fragments has been achieved by light-dependent coupling procedures. Anti-alpha-foetoprotein (anti-AFP) monoclonal antibodies were covalently linked to microplates by layer-coating procedures, which entail antibody photoimmobilization to a photolinker-polymer-precoated surface. In this and the co-coating procedure described, diazirine-functionalized BSA (T-BSA) served as the multifunctional light-activatable linking agent (photolinker polymer). Prior to photo-activation, F(ab')2 or F(ab') fragments derived from anti-(prostate-specific antigen) monoclonal antibodies were mixed and co-coated with the photolinker polymer on to polystyrene microplates. The immunoreagents remained immunologically active after 350 nm irradiation (irradiance 0.7 mW.cm-2 for 20 min). Immuno-responses of photoimmobilized monoclonal anti-AFP antibodies were equivalent to signal intensities obtained with physically adsorbed antibodies. Photoimmobilization of anti-PSA F(ab') fragments in the presence of T-BSA revealed exponential binding characteristics indicating stabilizing molecular co-operativity of the BSA constituent. Co-coating procedures yielded 62 and 65% binding of applied 14C-labelled F(ab')2 and F(ab') fragments respectively. Covalency of antibody binding was inferred from: (i) the strict dependence of photoreagent availability; (ii) the light-dependence of the immobilization process; and (iii) the reversibility of immunocomplexation after acid treatment.

摘要

通过光依赖偶联程序实现了光交联剂聚合物介导的抗体、F(ab')和F(ab')2片段的共价固定。抗甲胎蛋白(抗AFP)单克隆抗体通过层涂程序共价连接到微孔板上,该程序需要将抗体光固定到预先涂有光交联剂聚合物的表面。在本程序以及所述的共涂程序中,重氮烷基化功能化牛血清白蛋白(T-BSA)用作多功能光可激活连接剂(光交联剂聚合物)。在光激活之前,将源自抗(前列腺特异性抗原)单克隆抗体的F(ab')2或F(ab')片段与光交联剂聚合物混合并共涂到聚苯乙烯微孔板上。在350nm照射后(辐照度0.7mW·cm-2,持续20分钟),免疫试剂仍保持免疫活性。光固定的抗AFP单克隆抗体的免疫反应与物理吸附抗体获得的信号强度相当。在T-BSA存在下抗PSA F(ab')片段的光固定显示出指数结合特性,表明BSA成分具有稳定的分子协同作用。共涂程序分别使应用的14C标记的F(ab')2和F(ab')片段的结合率达到62%和65%。抗体结合的共价性可从以下方面推断:(i)光试剂可用性的严格依赖性;(ii)固定过程的光依赖性;以及(iii)酸处理后免疫复合物形成的可逆性。

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