Pajor Ana M, Sun Nina N, Joshi Aditya D, Randolph Kathleen M
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California-San Diego, La Jolla, CA 92093-0718, USA.
Biochim Biophys Acta. 2011 Jun;1808(6):1454-61. doi: 10.1016/j.bbamem.2010.11.007. Epub 2010 Nov 10.
Citric acid cycle intermediates, including succinate and citrate, are absorbed across the apical membrane by the NaDC1 Na+/dicarboxylate cotransporter located in the kidney and small intestine. The secondary structure model of NaDC1 contains 11 transmembrane helices (TM). TM7 was shown previously to contain determinants of citrate affinity, and Arg-349 at the extracellular end of the helix is required for transport. The present study involved cysteine scanning mutagenesis of 26 amino acids in TM7 and the associated loops. All of the mutants were well expressed on the plasma membrane, but many had low or no transport activity: 6 were inactive and 7 had activity less than 25% of the parental. Three of the mutants had notable changes in functional properties. F336C had increased transport activity due to an increased Vmax for succinate. The conserved residue F339C had very low transport activity and a change in substrate selectivity. G356C in the putative extracellular loop was the only cysteine mutant that was affected by the membrane-impermeant cysteine reagent, MTSET. However, direct labeling of G356C with MTSEA-biotin gave a weak signal, indicating that this residue is not readily accessible to more bulky reagents. The results suggest that the amino acids of TM7 are functionally important because their replacement by cysteine had large effects on transport activity. However, most of TM7 does not appear to be accessible to the extracellular fluid and is likely to be an outer helix in contact with the lipid bilayer.
柠檬酸循环中间体,包括琥珀酸和柠檬酸,通过位于肾脏和小肠中的NaDC1(Na+/二羧酸盐共转运蛋白)跨顶端膜被吸收。NaDC1的二级结构模型包含11个跨膜螺旋(TM)。先前已表明TM7包含柠檬酸亲和力的决定因素,并且螺旋细胞外端的精氨酸-349是转运所必需的。本研究涉及对TM7及其相关环中26个氨基酸进行半胱氨酸扫描诱变。所有突变体均在质膜上良好表达,但许多突变体具有低转运活性或无转运活性:6个无活性,7个活性低于亲本的25%。其中三个突变体在功能特性上有显著变化。F336C由于琥珀酸的Vmax增加而具有增加的转运活性。保守残基F339C具有非常低的转运活性和底物选择性的变化。推定的细胞外环中的G356C是唯一受膜不透性半胱氨酸试剂MTSET影响的半胱氨酸突变体。然而,用MTSEA-生物素直接标记G356C产生的信号较弱,表明该残基不易被更大的试剂接近。结果表明,TM7的氨基酸在功能上很重要,因为它们被半胱氨酸取代对转运活性有很大影响。然而,TM7的大部分似乎无法接触细胞外液,可能是与脂质双层接触的外部螺旋。