Abramson Jeff, Smirnova Irina, Kasho Vladimir, Verner Gillian, Kaback H Ronald, Iwata So
Department of Biological Sciences, Imperial College London, London SW7 2AZ, UK.
Science. 2003 Aug 1;301(5633):610-5. doi: 10.1126/science.1088196.
Membrane transport proteins that transduce free energy stored in electrochemical ion gradients into a concentration gradient are a major class of membrane proteins. We report the crystal structure at 3.5 angstroms of the Escherichia coli lactose permease, an intensively studied member of the major facilitator superfamily of transporters. The molecule is composed of N- and C-terminal domains, each with six transmembrane helices, symmetrically positioned within the permease. A large internal hydrophilic cavity open to the cytoplasmic side represents the inward-facing conformation of the transporter. The structure with a bound lactose homolog, beta-D-galactopyranosyl-1-thio-beta-D-galactopyranoside, reveals the sugar-binding site in the cavity, and residues that play major roles in substrate recognition and proton translocation are identified. We propose a possible mechanism for lactose/proton symport (co-transport) consistent with both the structure and a large body of experimental data.
能将电化学离子梯度中储存的自由能转化为浓度梯度的膜转运蛋白是一类主要的膜蛋白。我们报告了大肠杆菌乳糖通透酶的3.5埃晶体结构,该通透酶是转运蛋白主要促进剂超家族中经过深入研究的成员。该分子由N端和C端结构域组成,每个结构域都有六个跨膜螺旋,在通透酶内对称定位。一个通向细胞质侧的大的内部亲水腔代表了转运蛋白的内向构象。结合了乳糖类似物β-D-吡喃半乳糖基-1-硫代-β-D-吡喃半乳糖苷的结构揭示了腔内的糖结合位点,并确定了在底物识别和质子转运中起主要作用的残基。我们提出了一种与结构和大量实验数据相一致的乳糖/质子同向转运(共转运)的可能机制。