López-Ribot J L, Alloush H M, Masten B J, Chaffin W L
Department of Microbiology and Immunology, Texas Tech University Health Sciences Center, Lubbock 79430, USA.
Infect Immun. 1996 Aug;64(8):3333-40. doi: 10.1128/iai.64.8.3333-3340.1996.
We have previously reported the isolation of several clones from a cDNA expression library from Candida albicans, one of which was associated with a constitutively expressed 70-kDa protein. The moiety was present in the beta-mercaptoethanol extracts of cell walls from both blastoconidia and germ tubes. The surface expression of this moiety was revealed by an indirect immunofluorescence assay using affinity-purified antibody to the fusion protein produced by the clone. The 0.68-kb cDNA insert was sequenced. A database search revealed extensive homology with the 70-kDa family of stress or heat shock proteins (hsps). The 77% homology with another C. albicans HSP70 sequence suggested that this fragment represented a second member of the HSP70 family in this organism. Homology ranging from 65 to 76% was observed with members of four subfamilies (SSA, SSB, SSC, and SSD) of the Saccharomyces cerevisiae HSP70 gene family. The nucleic acid sequence and the deduced amino acid sequence of the open reading frame showed greatest homology with SSA1 and SSA2 sequences, and the gene corresponding to the cDNA clone was designated C. albicans SSA2. The relationship with the SSA family was supported by reactivity of the 70-kDa component with antibody recognizing the Ssa proteins of S. cerevisiae. The presence of an hsp70 in the cell wall was confirmed by two additional methods. Cell wall proteins were biotinylated with a non-membrane-permeable derivative to distinguish extracellular from cytosolic proteins. Biotinylated hsp70 was detected by Western blotting (immunoblotting) among the biotinylated components affinity purified by chromatography on streptavidin, thereby establishing its presence in the cell wall. Immunoelectron microscopy showed that the 70-kDa component was present at the cell surface as well as the outer surface of the plasma membrane and extended through the cell wall, occasionally appearing to reach the cell surface through channels. Northern (RNA) blot analysis showed that the gene was expressed in yeast cells growing in yeast extract-peptone medium at both 25 and 37 degrees C and in Lee medium at 25 degrees C and during formation of germ tubes in Lee medium 37 degrees C. No obvious increase in the expression level was detected after the temperature shift. Members of the hsp70 family have been reported to be immunoreactive. The fusion protein produced by the cDNA clone was recognized by serum from healthy individuals and patients with candidiasis. Since members of the hsp70 family of eucaryotic proteins are associated with chaperone and translocation functions, in addition to being immunogenic, this protein may play a role in the assembly and function of other cell wall proteins.
我们之前报道过从白色念珠菌的cDNA表达文库中分离出几个克隆,其中一个与一种组成型表达的70 kDa蛋白相关。该部分存在于芽生孢子和芽管细胞壁的β-巯基乙醇提取物中。使用针对该克隆产生的融合蛋白的亲和纯化抗体,通过间接免疫荧光测定法揭示了该部分的表面表达。对0.68 kb的cDNA插入片段进行了测序。数据库搜索显示与应激或热休克蛋白(hsps)的70 kDa家族有广泛的同源性。与另一个白色念珠菌HSP70序列77%的同源性表明,该片段代表了该生物体中HSP70家族的第二个成员。与酿酒酵母HSP70基因家族的四个亚家族(SSA、SSB、SSC和SSD)的成员观察到65%至76%的同源性。开放阅读框的核酸序列和推导的氨基酸序列与SSA1和SSA2序列显示出最大的同源性,与该cDNA克隆对应的基因被命名为白色念珠菌SSA2。70 kDa成分与识别酿酒酵母Ssa蛋白的抗体的反应性支持了与SSA家族的关系。通过另外两种方法证实了细胞壁中存在hsp70。用一种非膜渗透性衍生物对细胞壁蛋白进行生物素化,以区分细胞外蛋白和胞质蛋白。通过蛋白质印迹法(免疫印迹法)在通过抗生物素蛋白链菌素色谱法亲和纯化的生物素化成分中检测到生物素化的hsp70,从而确定其在细胞壁中的存在。免疫电子显微镜显示,70 kDa成分存在于细胞表面以及质膜的外表面,并延伸穿过细胞壁,偶尔似乎通过通道到达细胞表面。Northern(RNA)印迹分析表明,该基因在酵母提取物-蛋白胨培养基中于25℃和37℃生长的酵母细胞中、在25℃的Lee培养基中以及在Lee培养基中于37℃形成芽管的过程中均有表达。温度变化后未检测到表达水平有明显增加。据报道,hsp70家族的成员具有免疫反应性。该cDNA克隆产生的融合蛋白被健康个体和念珠菌病患者的血清识别。由于真核生物蛋白的hsp70家族成员除了具有免疫原性外,还与伴侣和转运功能相关,因此该蛋白可能在其他细胞壁蛋白的组装和功能中发挥作用。