Nelson B D, Traxler B
Department of Microbiology, University of Washington, Seattle 98195-7242, USA.
J Bacteriol. 1998 May;180(9):2507-14. doi: 10.1128/JB.180.9.2507-2514.1998.
The maltose transport complex of Escherichia coli is a well-studied example of an ATP-binding cassette transporter. The complex, containing one copy each of the integral membrane proteins MalG and MalF and two copies of the peripheral cytoplasmic membrane protein MalK, interacts with the periplasmic maltose-binding protein to efficiently translocate maltose and maltodextrins across the bacterial cytoplasmic membrane. To investigate the role of MalG both in MalFGK2 assembly interactions and in subsequent transport interactions, we isolated and characterized 18 different MalG mutants, each containing a 31-residue insertion in the protein. Eight insertions mapping to distinct hydrophilic regions of MalG permitted either assembly or both assembly and transport interactions to occur. In particular, we isolated two insertions mapping to extracytoplasmic (periplasmic) regions of MalG which preserved both assembly and transport abilities, suggesting that these are permissive sites in the protein. Another periplasmic insertion seems to affect only transport-specific interactions between MalG and maltose-binding protein, defining a novel class of MalG mutants. Finally, four MalG mutant proteins, although stably expressed, are unable to assemble into the MalFGK2 complex. These mutants contain insertions in only two different hydrophilic regions of MalG, consistent with the notion that a restricted number of domains in this protein are critical complex assembly determinants. These MalG mutants will allow us to further explore the intermolecular interactions of this model transporter.
大肠杆菌的麦芽糖转运复合体是一种经过充分研究的ATP结合盒式转运蛋白的实例。该复合体包含一份完整膜蛋白MalG和MalF以及两份外周细胞质膜蛋白MalK,它与周质麦芽糖结合蛋白相互作用,以有效地将麦芽糖和麦芽糊精转运穿过细菌细胞质膜。为了研究MalG在MalFGK2组装相互作用以及后续转运相互作用中的作用,我们分离并鉴定了18种不同的MalG突变体,每个突变体在该蛋白中都有一个31个残基的插入。八个插入位点定位于MalG不同的亲水区,允许组装或同时允许组装和转运相互作用发生。特别是,我们分离出两个定位于MalG胞外(周质)区域的插入位点,它们保留了组装和转运能力,这表明这些是该蛋白中的允许位点。另一个周质插入似乎仅影响MalG与麦芽糖结合蛋白之间的转运特异性相互作用,定义了一类新型的MalG突变体。最后,四种MalG突变蛋白虽然稳定表达,但无法组装成MalFGK2复合体。这些突变体仅在MalG的两个不同亲水区有插入,这与该蛋白中有限数量的结构域是关键复合体组装决定因素的观点一致。这些MalG突变体将使我们能够进一步探索这种模型转运蛋白的分子间相互作用。