Wilson M, Moore J, Kieser J B
J Clin Periodontol. 1986 Sep;13(8):743-7. doi: 10.1111/j.1600-051x.1986.tb00876.x.
A new approach has been developed to circumvent the problems of false positive reactions in the Limulus Amoebocyte Lysate (LAL) assay for lipopolysaccharide (LPS) in root surface materials. These LAL-reactive materials include thrombin, thromboplastin, ribonuclease, ribonucleic acid, lipoteichoic acid and peptidoglycan fragments. In the present study, hot phenol/water extraction of these substances followed by ultracentrifugation of the resulting aqueous phases reduced their concentrations to very low levels. Furthermore, the application of Polymyxin B/Sepharose 4B affinity chromatography to these extracts enabled their intrinsic LAL-activity to be determined. Use of these techniques to assay root surface materials has identified LPS as being the major LAL-reactive material present. The mean LPS yield for the periodontally involved teeth was 4.13 micrograms/tooth, representing 2.82 micrograms/root. In contrast, the mean yield of LPS for the periodontally uninvolved teeth was 3.12 ng/tooth.
已经开发出一种新方法来规避在检测牙根表面材料中脂多糖(LPS)的鲎试剂(LAL)试验中出现假阳性反应的问题。这些与LAL反应的物质包括凝血酶、凝血活酶、核糖核酸酶、核糖核酸、脂磷壁酸和肽聚糖片段。在本研究中,用热酚/水萃取这些物质,然后对所得水相进行超速离心,可将其浓度降低至非常低的水平。此外,将多粘菌素B/琼脂糖4B亲和色谱法应用于这些提取物,能够测定其内在的LAL活性。使用这些技术检测牙根表面材料已确定LPS是主要的LAL反应性物质。牙周受累牙齿的平均LPS产量为4.13微克/颗牙,相当于2.82微克/根。相比之下,牙周未受累牙齿的LPS平均产量为3.12纳克/颗牙。