López-Llano Jon, Maldonado Susana, Bueno Marta, Lostao Anabel, Angeles-Jiménez Maria, Lillo Mariá P, Sancho Javier
Biocomputation and Complex Systems Physics Institute, Universidad de Zaragoza, Zaragoza, Spain.
J Biol Chem. 2004 Nov 5;279(45):47177-83. doi: 10.1074/jbc.M405792200. Epub 2004 Aug 17.
Flavodoxins are well known one-domain alpha/beta electron-transfer proteins that, according to the presence or absence of a approximately 20-residue loop splitting the fifth beta-strand of the central beta-sheet, have been classified in two groups: long and short-chain flavodoxins, respectively. Although the flavodoxins have been extensively used as models to study electron transfer, ligand binding, protein stability and folding issues, the role of the loop has not been investigated. We have constructed two shortened versions of the long-chain Anabaena flavodoxin in which the split beta-strand has been spliced to remove the original loop. The two variants have been carefully analyzed using various spectroscopic and hydrodynamic criteria, and one of them is clearly well folded, indicating that the long loop is a peripheral element of the structure of long flavodoxins. However, the removal of the loop (which is not in contact with the cofactor in the native structure) markedly decreases the affinity of the apoflavodoxin-FMN complex. This seems related to the fact that, in long flavodoxins, the adjacent tyrosine-bearing FMN binding loop (which is longer and thus more flexible than in short flavodoxins) is stabilized in its competent conformation by interactions with the excised loop. The modest role played by the long loop of long flavodoxins in the structure of these proteins (and in its conformational stability, see Lopez-Llano, J., Maldonado, S., Jain, S., Lostao, A., Godoy-Ruiz, R., Sanchez-Ruiz, Cortijo, M., Fernandez-Recio, J., and Sancho, J. (2004) J. Biol. Chem. 279, 47184-47191) opens the possibility that its conservation in so many species is related to a functional role yet to be discovered. In this respect, we discuss the possibility that the long loop is involved in the recognition of some flavodoxin partners. In addition, we report on a structural feature of flavodoxins that could indicate that the short flavodoxins derive from the long ones.
黄素氧还蛋白是众所周知的单结构域α/β电子传递蛋白,根据是否存在一个约20个残基的环(该环将中央β折叠的第五条β链分开),可分为两组:长链黄素氧还蛋白和短链黄素氧还蛋白。尽管黄素氧还蛋白已被广泛用作研究电子传递、配体结合、蛋白质稳定性和折叠问题的模型,但该环的作用尚未得到研究。我们构建了长链鱼腥藻黄素氧还蛋白的两个缩短版本,其中分开的β链已被拼接以去除原始环。使用各种光谱和流体动力学标准对这两个变体进行了仔细分析,其中一个明显折叠良好,表明长环是长链黄素氧还蛋白结构的外围元件。然而,去除该环(在天然结构中不与辅因子接触)显著降低了脱辅基黄素氧还蛋白 - FMN复合物的亲和力。这似乎与以下事实有关:在长链黄素氧还蛋白中,相邻的含酪氨酸的FMN结合环(比短链黄素氧还蛋白中的更长,因此更灵活)通过与切除的环相互作用而稳定在其有效构象中。长链黄素氧还蛋白的长环在这些蛋白质的结构中所起的适度作用(以及其构象稳定性,见Lopez - Llano, J., Maldonado, S., Jain, S., Lostao, A., Godoy - Ruiz, R., Sanchez - Ruiz, Cortijo, M., Fernandez - Recio, J., and Sancho, J. (2004) J. Biol. Chem. 279, 47184 - 47191)使得其在如此多物种中的保守性可能与尚未发现的功能作用有关。在这方面,我们讨论了长环参与识别某些黄素氧还蛋白伴侣的可能性。此外,我们报道了黄素氧还蛋白的一个结构特征,该特征可能表明短链黄素氧还蛋白源自长链黄素氧还蛋白。