Department of Biochemistry, University of Delhi, New Delhi, India.
PLoS One. 2010 Feb 15;5(2):e9222. doi: 10.1371/journal.pone.0009222.
Mycobacterium tuberculosis (Mtb), a dreaded pathogen, has a unique cell envelope composed of high fatty acid content that plays a crucial role in its pathogenesis. Acetyl Coenzyme A Carboxylase (ACC), an important enzyme that catalyzes the first reaction of fatty acid biosynthesis, is biotinylated by biotin acetyl-CoA carboxylase ligase (BirA). The ligand-binding loops in all known apo BirAs to date are disordered and attain an ordered structure only after undergoing a conformational change upon ligand-binding. Here, we report that dehydration of Mtb-BirA crystals traps both the apo and active conformations in its asymmetric unit, and for the first time provides structural evidence of such transformation. Recombinant Mtb-BirA was crystallized at room temperature, and diffraction data was collected at 295 K as well as at 120 K. Transfer of crystals to paraffin and paratone-N oil (cryoprotectants) prior to flash-freezing induced lattice shrinkage and enhancement in the resolution of the X-ray diffraction data. Intriguingly, the crystal lattice rearrangement due to shrinkage in the dehydrated Mtb-BirA crystals ensued structural order of otherwise flexible ligand-binding loops L4 and L8 in apo BirA. In addition, crystal dehydration resulted in a shift of approximately 3.5 A in the flexible loop L6, a proline-rich loop unique to Mtb complex as well as around the L11 region. The shift in loop L11 in the C-terminal domain on dehydration emulates the action responsible for the complex formation with its protein ligand biotin carboxyl carrier protein (BCCP) domain of ACCA3. This is contrary to the involvement of loop L14 observed in Pyrococcus horikoshii BirA-BCCP complex. Another interesting feature that emerges from this dehydrated structure is that the two subunits A and B, though related by a noncrystallographic twofold symmetry, assemble into an asymmetric dimer representing the ligand-bound and ligand-free states of the protein, respectively. In-depth analyses of the sequence and the structure also provide answers to the reported lower affinities of Mtb-BirA toward ATP and biotin substrates. This dehydrated crystal structure not only provides key leads to the understanding of the structure/function relationships in the protein in the absence of any ligand-bound structure, but also demonstrates the merit of dehydration of crystals as an inimitable technique to have a glance at proteins in action.
结核分枝杆菌(Mtb)是一种令人恐惧的病原体,它具有独特的细胞包膜,其高脂肪酸含量在其发病机制中起着至关重要的作用。乙酰辅酶 A 羧化酶(ACC)是催化脂肪酸生物合成第一步反应的重要酶,由生物素酰基辅酶 A 羧化酶连接酶(BirA)生物素化。迄今为止,所有已知的 apo BirA 的配体结合环都是无序的,并且只有在配体结合后经历构象变化才能获得有序结构。在这里,我们报告说,Mtb-BirA 晶体的脱水会在其不对称单元中捕获 apo 和活性构象,并且首次提供了这种转化的结构证据。重组 Mtb-BirA 在室温下结晶,衍射数据在 295 K 以及 120 K 下收集。在将晶体转移到石蜡和 paraffinone-N 油(cryoprotectants)之前进行闪光冷冻会导致晶格收缩,并提高 X 射线衍射数据的分辨率。有趣的是,由于脱水 Mtb-BirA 晶体的晶格重排,apo BirA 中原本柔性的配体结合环 L4 和 L8 变得有序。此外,晶体脱水导致柔性环 L6 约 3.5 A 的移动,L6 是 Mtb 复合物特有的富含脯氨酸的环,以及 L11 区域周围。脱水后 C 末端结构域中 L11 环的移动模拟了与蛋白配体 ACCA3 的生物素羧基载体蛋白(BCCP)域形成复合物的作用。这与在 Pyrococcus horikoshii BirA-BCCP 复合物中观察到的 L14 环的参与相反。另一个有趣的特征是,两个亚基 A 和 B 虽然通过非晶体学的两倍对称相关,但组装成不对称二聚体,分别代表蛋白的配体结合和配体自由状态。对序列和结构的深入分析也为 Mtb-BirA 对 ATP 和生物素底物的报道的较低亲和力提供了答案。这种脱水晶体结构不仅为在没有任何配体结合结构的情况下理解蛋白的结构/功能关系提供了关键线索,而且还证明了晶体脱水作为一种独特的技术来观察蛋白活性的优点。