Kaback H R, Wu J
Howard Hughes Medical Institute, Departments of Physiology, University of California Los Angeles 90024-1662, USA.
Q Rev Biophys. 1997 Nov;30(4):333-64. doi: 10.1017/s0033583597003387.
The lac permease of E. coli is a paradigm for secondary active transporter proteins that transduce the free energy stored in electrochemical ion gradients into work in the form of a concentration gradient. This hydrophobic, polytopic, cytoplasmic membrane protein catalyses the coupled, stoichiometric translocation of beta-galactosides and H+, and it has been solubilized, purified, reconstituted into artificial phospholipid vesicles and shown to be solely responsible responsible for beta-galactoside transport as a monomer. The lacY gene which encodes the permease has been cloned and sequenced, and all available evidence indicates that the protein has 12 transmembrane domains in alpha-helical configuration that traverse the membrane in zigzag fashion connected by hydrophilic loops with the N and C termini on the cytoplasmic face of the membrane. Extensive use of site-directed and Cys-scanning mutagenesis indicates that very few residues in the permease are directly involved in the transport mechanism, but the permease appears to be a highly flexible protein that undergoes widespread conformational changes during turnover. Based on a variety of site-directed approaches which include second-site suppressor analysis and site-directed mutagenesis, excimer fluorescence, engineered divalent metal binding sites, chemical cleavage, EPR, thiol crosslinking and identification of discontinuous mAb epitopes, a helix packing model has been formulated.A mechanism for the coupled translocate ion of substrate and H+ by the lac permease of E. coli is proposed. Four residues are irreplaceable with respect to coupling, and the residues are paired in the tertiary structure--Arg-302 (helix IX) with Glu-325 (helix 10) and His-322 (helix 10) with Glu-269 (helix VIII). In an adjacent region of the molecule at the interface between helices VIII and V is the substrate translocation pathway in which Glu-126 and Arg-144 appear to play key roles. Because of this arrangement, interfacial changes between helices VIII and V are transmitted to the interface between helices IX and X and vice versa. Upon ligand binding, a structural change at the interface between helices V and VIII disrupts the interaction between Glu-269 and His-322, Glu-269 displaces Glu-325 from Ag-302 and Glu-325 is protonated.Simultaneously, protonated Glu-325 becomes inaccessible to water which drastically increases its pKa. In this configuration, the permease undergoes a freely reversible conformational change that corresponds to translocation of the ternary complex. In order to return to ground state after release of substrate, the Arg-302-Glu-325 interaction must be reestablished which necessitates loss of H+ from Glu-325. The H+ is released into a water-filled crevice between helices IX and X which becomes transiently accessible to both sides of the membrane due to a change in helix tilt, where it is acted upon equally by either the membrane potential or the pH gradient across the membrane. Remarkably few amino-acid residues appear to be critically involved in the transport mechanism of lac permease, suggesting that relatively simple chemistry drives the mechanism. On the other hand, widespread, cooperative conformational changes appear to be involved in turnover. As a whole the data suggest that the 12 helices which comprise the permease are loosely packed with a considerable amount of water in the interstices and that surface contours are important for sliding or tilting motions that occur during turnover. This surmise coupled with the indication that few residues are essential to the mechanism is encouraging in that it suggest that the possibility that a relatively low resolution structure (i.e. helix packing) plus localization of the critical residues and the translocation pathway can provide important insights into the mechanism. (ABSTRACT TRUNCATED)
大肠杆菌的乳糖通透酶是次级主动转运蛋白的范例,它将电化学离子梯度中储存的自由能转化为浓度梯度形式的功。这种疏水性、多结构域的细胞质膜蛋白催化β-半乳糖苷和H⁺的偶联、化学计量转运,它已被溶解、纯化、重组成人工磷脂囊泡,并被证明作为单体单独负责β-半乳糖苷的转运。编码通透酶的lacY基因已被克隆和测序,所有现有证据表明该蛋白具有12个α-螺旋构型的跨膜结构域,这些结构域以锯齿状方式穿过膜,由亲水环连接,N和C末端位于膜的细胞质面。定点诱变和半胱氨酸扫描诱变的广泛应用表明,通透酶中直接参与转运机制的残基很少,但通透酶似乎是一种高度灵活的蛋白,在周转过程中会发生广泛的构象变化。基于多种定点方法,包括第二位点抑制分析和定点诱变、准分子荧光、工程化二价金属结合位点、化学裂解、电子顺磁共振、硫醇交联以及不连续单克隆抗体表位的鉴定,已构建了一个螺旋堆积模型。提出了大肠杆菌乳糖通透酶偶联转运底物和H⁺的机制。有四个残基在偶联方面是不可替代的,这些残基在三级结构中配对——螺旋IX中的精氨酸-302与螺旋10中的谷氨酸-325以及螺旋10中的组氨酸-322与螺旋VIII中的谷氨酸-269。在分子中螺旋VIII和V之间界面的相邻区域是底物转运途径,其中谷氨酸-126和精氨酸-144似乎起关键作用。由于这种排列,螺旋VIII和V之间的界面变化会传递到螺旋IX和X之间的界面,反之亦然。配体结合后,螺旋V和VIII之间界面的结构变化破坏了谷氨酸-269和组氨酸-322之间的相互作用,谷氨酸-269将谷氨酸-325从精氨酸-302上取代,谷氨酸-325被质子化。同时,质子化的谷氨酸-325变得无法与水接触,这极大地提高了其pKa。在这种构型下,通透酶经历一个自由可逆的构象变化,这对应于三元复合物的转运。为了在底物释放后回到基态,必须重新建立精氨酸-302-谷氨酸-325的相互作用,这需要谷氨酸-325失去H⁺。H⁺被释放到螺旋IX和X之间的一个充满水的裂缝中,由于螺旋倾斜的变化,这个裂缝对膜的两侧暂时变得可及,在那里它受到膜电位或跨膜pH梯度的同等作用。明显很少有氨基酸残基似乎在乳糖通透酶的转运机制中起关键作用,这表明相对简单的化学过程驱动了该机制。另一方面,广泛的、协同的构象变化似乎参与了周转。总体而言,数据表明构成通透酶的12个螺旋松散堆积,间隙中有大量的水,并且表面轮廓对于周转过程中发生的滑动或倾斜运动很重要。这种推测加上很少有残基对该机制至关重要的迹象令人鼓舞,因为它表明相对低分辨率的结构(即螺旋堆积)加上关键残基和转运途径的定位有可能为该机制提供重要见解。(摘要截断)