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脂质A中的四糖L-α-D-庚糖1→2-L-α-D-庚糖1→3-L-α-D-庚糖1→(3-脱氧-D-甘露糖辛酮酸)和磷酸定义了被单克隆抗体识别的嗜血杆菌脂多糖中的保守表位。

The tetrasaccharide L-alpha-D-heptose1-->2-L-alpha-D-heptose1--> 3-L-alpha-D-heptose1-->(3-deoxy-D-manno-octulosonic acid) and phosphate in lipid A define the conserved epitope in Haemophilus lipopolysaccharides recognized by a monoclonal antibody.

作者信息

Borrelli S, Hegedus O, Shaw D H, Jansson P E, Lindberg A A

机构信息

Department of Immunology, Microbiology, Pathology and Infectious Diseases, Karolinska Institute, Huddinge, Sweden.

出版信息

Infect Immun. 1995 Sep;63(9):3683-92. doi: 10.1128/iai.63.9.3683-3692.1995.

Abstract

A murine monoclonal antibody, MAHI 3 (immunoglobulin G2b), that is broadly reactive with Haemophilus influenzae lipopolysaccharides (LPSs) but nonreactive with all enterobacterial LPSs tested was generated by fusing mouse myeloma cells with spleen cells of BALB/c mice immunized with azide-killed H. influenzae RM.7004. MAHI 3 bound to all H. influenzae, all other human Haemophilus spp., all Bordetella pertussis and Bordetella parapertussis, and all Aeromonas spp. tested but not to any Neisseria or Moraxella catarrhalis strains, as determined by enzyme immunoassay, colony dot immunoblotting, and immunoblotting. In an inhibition enzyme immunoassay, MAHI 3 reacted with all 45 H. influenzae LPSs tested but not with the LPS from the rough mutant I69 Rd-/b+, which has only 3-deoxy-D-manno-octulosonic acid (P) [Kdo(P)] and lipid A. The antibody was not inhibited by H. influenzae lipid A or lipid-free polysaccharide isolated after mild acid hydrolysis. Only native LPSs show positive inhibitory activity, indicating that part of lipid A is involved in the binding of MAHI 3. From the results, it is indicated that the structural element recognized by MAHI 3 is Hep alpha 1-->2Hep alpha 1-->3Hep alpha 1-->Kdo together with part of lipid A, including the phosphate.

摘要

通过将小鼠骨髓瘤细胞与用叠氮化钠杀死的流感嗜血杆菌RM.7004免疫的BALB/c小鼠的脾细胞融合,产生了一种鼠单克隆抗体MAHI 3(免疫球蛋白G2b),它与流感嗜血杆菌脂多糖(LPS)具有广泛反应性,但与所有测试的肠杆菌LPS无反应。通过酶免疫测定、菌落斑点免疫印迹和免疫印迹确定,MAHI 3与所有流感嗜血杆菌、所有其他人类嗜血杆菌属、所有百日咳博德特氏菌和副百日咳博德特氏菌以及所有测试的气单胞菌属结合,但不与任何奈瑟菌或卡他莫拉菌菌株结合。在抑制酶免疫测定中,MAHI 3与所有测试的45种流感嗜血杆菌LPS反应,但不与粗糙突变体I69 Rd-/b+的LPS反应,该突变体仅具有3-脱氧-D-甘露糖辛酮酸(P)[Kdo(P)]和脂质A。该抗体不受流感嗜血杆菌脂质A或轻度酸水解后分离的无脂质多糖的抑制。只有天然LPS显示出阳性抑制活性,表明脂质A的一部分参与了MAHI 3的结合。从结果表明,MAHI 3识别的结构元件是Hepα1→2Hepα1→3Hepα1→Kdo以及脂质A的一部分,包括磷酸。

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