Pupo E, Aguila A, Santana H, Núñez J F, Castellanos-Serra L, Hardy E
Center for Genetic Engineering and Biotechnology, Havana, Cuba.
Electrophoresis. 1999 Mar;20(3):458-61. doi: 10.1002/(SICI)1522-2683(19990301)20:3<458::AID-ELPS458>3.0.CO;2-3.
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.
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。