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重组HtrA的特性:一种来自不可分型流感嗜血杆菌的中耳炎疫苗候选抗原。

Properties of recombinant HtrA: an otitis media vaccine candidate antigen from non-typeable Haemophilus influenzae.

作者信息

Cates G A, Yang Y P, Klyushnichenko V, Oomen R, Loosmore S M

机构信息

Aventis Pasteur, Toronto, Ontario, Canada.

出版信息

Dev Biol (Basel). 2000;103:201-4.

Abstract

Non-encapsulated or non-typable Haemophilus influenzae (NTHi) is a major cause of middle ear infections in young children. HtrA has been identified as a vaccine candidate antigen from NTHi; therefore physicochemical characterization of this antigen is important for vaccine development. Recombinant NTHi HtrA has been expressed in E. coli and shown to have serine protease activity. Several mutant, recombinant HtrA proteins were expressed and purified to obtain suitable vaccine antigens lacking protease activity. Two mutants with alterations at the putative active site His91 and Ser197, designated H91A and S197A were examined by circular dichroic spectropolarimetry (CD) to evaluate secondary structure. The S197A mutant had a more random secondary structure compared to wild-type rHtrA or H91A. It is likely that improper folding of S197A accounts for its lack of immunoprotective properties in a chinchilla model of otitis media.

摘要

非包膜或不可分型的流感嗜血杆菌(NTHi)是幼儿中耳感染的主要原因。HtrA已被确定为NTHi的一种候选疫苗抗原;因此,对该抗原进行物理化学特性分析对于疫苗开发很重要。重组NTHi HtrA已在大肠杆菌中表达,并显示具有丝氨酸蛋白酶活性。表达并纯化了几种突变的重组HtrA蛋白,以获得缺乏蛋白酶活性的合适疫苗抗原。通过圆二色光谱偏振法(CD)检测了两个在假定活性位点His91和Ser197发生改变的突变体,分别命名为H91A和S197A,以评估其二级结构。与野生型rHtrA或H91A相比,S197A突变体具有更随机的二级结构。在中耳炎的栗鼠模型中,S197A折叠不当可能是其缺乏免疫保护特性的原因。

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