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利用合成脂肽对流感嗜血杆菌外膜蛋白P6的抗原表位和免疫原表位进行定位

Mapping of antigenic and immunogenic sites of Haemophilus influenzae outer membrane protein P6 using synthetic lipopeptides.

作者信息

Beck-Sickinger A G, Rotering H, Wiesmüller K H, Dorner F, Jung G

机构信息

Institut für Organische Chemie, Universität Tübingen, Germany.

出版信息

Biol Chem Hoppe Seyler. 1994 Mar;375(3):173-82. doi: 10.1515/bchm3.1994.375.3.173.

Abstract

The immune response to the P6 protein of Haemophilus influenzae was characterized with 24 synthetic icosapeptides and 45 dodecapeptides conjugated to the immune stimulator N-palmitoyl-S-[2,3-(bispalmitoyloxy)-(2RS)-propyl]-(R)-cysteinyl-( S)-serine . The antigenicity of these lipopeptides was investigated by enzyme-linked immunosorbent assays with rabbit anti-P6 serum. The epitopes of P6 protein were identified and localized within residues 31-46 and 59-70 and in the C-terminal part of the P6 protein. Mice were immunized with lipoicosapeptides without using additional adjuvants or carriers and the antibody titers were measured with isolated P6 protein and lipopeptides in a dot blot assay. Lipopeptides containing the sequence pattern QILDAHAA (P6 47-54) and the mouse B cell epitope GEYV (P6 43-46) induced high titers of anti P6 antibodies. These murine antibodies were able to neutralize the intact bacterium Haemophilus influenzae.

摘要

用24种合成二十肽和45种十二肽与免疫刺激剂N-棕榈酰-S-[2,3-(双棕榈酰氧基)-(2RS)-丙基] -(R)-半胱氨酰-(S)-丝氨酸偶联,对流感嗜血杆菌P6蛋白的免疫反应进行了表征。通过用兔抗P6血清进行酶联免疫吸附测定,研究了这些脂肽的抗原性。确定了P6蛋白的表位并将其定位在P6蛋白的31-46位残基、59-70位残基以及C末端部分。用脂二十肽免疫小鼠,不使用额外的佐剂或载体,并在斑点印迹试验中用分离的P6蛋白和脂肽测量抗体滴度。含有序列模式QILDAHAA(P6 47-54)和小鼠B细胞表位GEYV(P6 43-46)的脂肽诱导产生高滴度的抗P6抗体。这些鼠源抗体能够中和完整的流感嗜血杆菌。

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