首页> 美国卫生研究院文献>Journal of Bacteriology >Identification of a 521-Kilodalton Protein (Gli521) Involved in Force Generation or Force Transmission for Mycoplasma mobile Gliding
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Identification of a 521-Kilodalton Protein (Gli521) Involved in Force Generation or Force Transmission for Mycoplasma mobile Gliding

机译:521-千达尔顿蛋白(Gli521)的鉴定涉及支原体移动滑翔的力产生或力传递

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摘要

Several mycoplasma species are known to glide on solid surfaces such as glass in the direction of the membrane protrusion, but the mechanism underlying this movement is unknown. To identify a novel protein involved in gliding, we raised monoclonal antibodies against a detergent-insoluble protein fraction of Mycoplasma mobile, the fastest glider, and screened the antibodies for inhibitory effects on gliding. Five monoclonal antibodies stopped the movement of gliding mycoplasmas, keeping them on the glass surface, and all of them recognized a large protein in immunoblotting. This protein, named Gli521, is composed of 4,738 amino acids, has a predicted molecular mass of 520,559 Da, and is coded downstream of a gene for another gliding protein, Gli349, which is known to be responsible for glass binding during gliding. Edman degradation analysis indicated that the N-terminal region is processed at the peptide bond between the amino acid residues at positions 43 and 44. Analysis of gliding mutants isolated previously revealed that the Gli521 protein is missing in a nonbinding mutant, m9, where the gli521 gene is truncated by a nonsense mutation at the codon for the amino acid at position 1170. Immunofluorescence and immunoelectron microscopy indicated that Gli521 localizes all around the base of the membrane protrusion, at the “neck,” as previously observed for Gli349. Analysis of the inhibitory effects of the anti-Gli521 antibody on gliding motility revealed that this protein is responsible for force generation or force transmission, a role distinct from that of Gli349, and also suggested conformational changes of Gli349 and Gli521 during gliding.
机译:已知有几种支原体会在诸如玻璃之类的固体表面上沿膜突出的方向滑动,但是这种运动所基于的机制尚不清楚。为了鉴定与滑行有关的新型蛋白质,我们提出了针对最快的滑行器支原体流动性的去污剂不溶蛋白部分的单克隆抗体,并筛选了对滑行具有抑制作用的抗体。五种单克隆抗体阻止了滑动支原体的运动,将它们保持在玻璃表面上,并且它们都在免疫印迹中识别出一种大蛋白。该蛋白质名为Gli521,由4,738个氨基酸组成,预测的分子量为520,559 Da,编码在另一个滑动蛋白Gli349的基因下游,已知该蛋白与滑动过程中的玻璃结合有关。 Edman降解分析表明,N末端区域是在位置43和44的氨基酸残基之间的肽键处加工的。先前对滑动突变体的分析表明,在非结合突变体m9(其中gli521)中缺少Gli521蛋白该基因被1170位氨基酸的密码子无意义突变截断。免疫荧光和免疫电子显微镜检查表明,Gli521定位在整个膜突出基部的整个周围,在“颈部”,如先前对Gli349所观察到的。分析抗Gli521抗体对滑行运动的抑制作用后发现,该蛋白负责产生力或传递力,这与Gli349的作用不同,并且还暗示了滑行过程中Gli349和Gli521的构象变化。

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