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利用来自乳酸杆菌的新型细胞壁锚定蛋白,在乳酸乳球菌和植物乳杆菌中进行人乳头瘤病毒16型E7抗原的细胞表面展示。

Cell-surface display of E7 antigen from human papillomavirus type-16 in Lactococcus lactis and in Lactobacillus plantarum using a new cell-wall anchor from lactobacilli.

作者信息

Cortes-Perez Naima G, Azevedo Vasco, Alcocer-González Juan M, Rodriguez-Padilla Cristina, Tamez-Guerra Reyes S, Corthier Gérard, Gruss Alexandra, Langella Philippe, Bermúdez-Humarán Luis G

机构信息

Unité de Recherches Laitières et de Génétique Appliquée, INRA, Domaine de Vilvert, 78352, Jouy-en-Josas, cedex, France.

出版信息

J Drug Target. 2005 Feb;13(2):89-98. doi: 10.1080/10611860400024219.

Abstract

The human papillomavirus type-16 (HPV-16) E7 protein is considered a major viral oncoprotein involved in cervical cancer (CxCa) and a potential candidate for the development of a vaccine against this neoplasia. Here, two lactic acid bacteria (the model one Lactococcus lactis and a probiotic one Lactobacillus plantarum) were engineered to deliver an E7 mutant protein (E7mm), which has a reduced transforming activity and consequently, could fit better to therapeutic use in humans than the native form of E7. An efficient cell-surface display of E7mm was obtained in L. lactis using an expression cassette encoding a precursor composed of (i) the signal peptide and the first 15 amino acids of the mature part of the lactococcal Usp45 protein; (ii) E7mm and (iii) the cell-wall anchor of the Streptococcus pyogenes M6 protein (CWA(M6)). This hybrid precursor was produced but not cell-wall anchored in Lb. plantarum. We thus replaced CWA(M6) by the cell-wall anchor of a Lb. plantarum protein which allows an efficient cell-wall anchoring of E7mm in this bacterium. The E7mm production and cell-surface display in both L. lactis and a probiotic bacterium, Lb. plantarum, represent one more step towards the development of a safe and effective treatment against CxCa.

摘要

人乳头瘤病毒16型(HPV-16)E7蛋白被认为是参与宫颈癌(CxCa)的主要病毒癌蛋白,也是开发针对这种肿瘤的疫苗的潜在候选物。在此,对两种乳酸菌(模式菌乳酸乳球菌和益生菌植物乳杆菌)进行改造,以递送一种E7突变蛋白(E7mm),该蛋白的转化活性降低,因此与天然形式的E7相比,可能更适合用于人类治疗。使用编码由以下部分组成的前体的表达盒,在乳酸乳球菌中实现了E7mm在细胞表面的高效展示:(i)信号肽和乳酸乳球菌Usp45蛋白成熟部分的前15个氨基酸;(ii)E7mm;(iii)化脓性链球菌M6蛋白的细胞壁锚定结构域(CWA(M6))。这种杂交前体在植物乳杆菌中产生但未锚定在细胞壁上。因此,我们用一种植物乳杆菌蛋白的细胞壁锚定结构域取代了CWA(M6),该结构域可使E7mm在这种细菌中高效锚定在细胞壁上。在乳酸乳球菌和益生菌植物乳杆菌中生产E7mm并将其展示在细胞表面,是朝着开发安全有效的CxCa治疗方法又迈进了一步。

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