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用凝胶电泳微纯化的细菌脂多糖对小鼠进行免疫接种。

Mice immunization with gel electrophoresis-micropurified bacterial lipopolysaccharides.

作者信息

Pupo E, Aguila A, Santana H, Núñez J F, Castellanos-Serra L, Hardy E

机构信息

Center for Genetic Engineering and Biotechnology, Havana, Cuba.

出版信息

Electrophoresis. 1999 Mar;20(3):458-61. doi: 10.1002/(SICI)1522-2683(19990301)20:3<458::AID-ELPS458>3.0.CO;2-3.

Abstract

Some evidence on the possible use of sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) to elicit antibodies against smooth- or rough-type bacterial lipopolysaccharides (LPS) is shown. Gel-separated LPS were negatively stained with zinc-imidazole to precisely localize the bands of interest under fully reversible conditions. Then the bands of interest were excised and the resulting gel slices washed in a solution of a zinc-complexing agent (e.g., 100 mM EDTA), after which they were extruded through a metal sieve of 32 microm average size contained in a 1 mL syringe, to generate homogeneous gel microparticles. The LPS-containing gel slurries were used directly to immunize female BALB/c mice. Using this procedure, positive mouse polyclonal antibody responses against gel-purified smooth- or rough-LPS forms from Escherichia coli K-235 or Bordetella pertussis were elicited, as tested by a dot-immunoblotting assay. Our results may encourage the use of SDS-PAGE-micropurified LPS to develop optimized immunization procedures for the generation of specific antibodies against LPS bands of defined sizes, and therefore they constitute an intermediate step toward that aim.

摘要

展示了一些关于使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)引发针对光滑型或粗糙型细菌脂多糖(LPS)抗体的可能性的证据。凝胶分离的LPS用锌-咪唑进行负染色,以便在完全可逆的条件下精确地定位感兴趣的条带。然后切下感兴趣的条带,将所得的凝胶切片在锌络合剂溶液(例如100 mM EDTA)中洗涤,之后将其通过1 mL注射器中包含的平均尺寸为32微米的金属筛挤出,以产生均匀的凝胶微粒。含LPS的凝胶浆液直接用于免疫雌性BALB/c小鼠。通过该程序,引发了针对来自大肠杆菌K-235或百日咳博德特氏菌的凝胶纯化的光滑型或粗糙型LPS形式的阳性小鼠多克隆抗体反应,通过斑点免疫印迹分析进行测试。我们的结果可能会鼓励使用SDS-PAGE微纯化的LPS来开发优化的免疫程序,以产生针对特定大小的LPS条带的特异性抗体,因此它们构成了朝着该目标迈出的中间步骤。

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