Shimokawa N, Mori H, Ito K
Institute for Virus Research, Kyoto University, Sakyo-ku, Japan.
Mol Genet Genomics. 2003 May;269(2):180-7. doi: 10.1007/s00438-003-0804-8. Epub 2003 Feb 11.
To assess the functional importance of the transmembrane regions of SecY, we constructed a series of SecY variants, in which the six central residues of each transmembrane segment were replaced by amino acid residues from either transmembrane segment 3 or 4 of LacY. The SecY function, as assessed by the ability to complement cold-sensitive secYmutants with respect to their growth and translocase defects, was eliminated by the alterations in transmembrane segments 2, 3, 4, 7, 9 and 10. Among them, those in segments 3 and 4 had especially severe effects. In contrast, transmembrane segments 1, 5, 6, and 8 were more tolerant to the sequence alterations. The purified protein with an altered transmembrane segment 6 retained, in large measure, the ability to support SecA-dependent preprotein translocation in vitro. These results will help us to further understand how the SecYEG protein translocation channel functions.
为了评估SecY跨膜区域的功能重要性,我们构建了一系列SecY变体,其中每个跨膜段的六个中心残基被来自LacY跨膜段3或4的氨基酸残基取代。通过补充冷敏感secY突变体的生长和转位酶缺陷能力评估的SecY功能,被跨膜段2、3、4、7、9和10的改变消除。其中,跨膜段3和4的改变具有特别严重的影响。相比之下,跨膜段1、5、6和8对序列改变更具耐受性。跨膜段6改变的纯化蛋白在很大程度上保留了体外支持SecA依赖性前体蛋白转位的能力。这些结果将有助于我们进一步了解SecYEG蛋白转位通道的功能。