Deziel M R, Jung C Y, Rothstein A
Biochim Biophys Acta. 1985 Sep 25;819(1):83-92. doi: 10.1016/0005-2736(85)90198-1.
A preparation of band 4.5 protein of the red cell membrane, containing largely the sugar transporter, was labelled with the sulfhydryl reagent N-ethyl [14C]maleimide. In preparations denatured with sodium dodecyl sulfate (SDS), all five sulfhydryl groups present in the peptide, Mr 45 000 to 60 000, react with the alkylating agent within 20 min at 37 degrees C. If the peptide is reconstituted in lipid vesicles and cleaved with trypsin before extraction and denaturation with SDS, three sulfhydryl groups are found in a 30 kDa fragment and two in a 19 kDa fragment. In 'native' reconstituted protein only three groups react, even after two hours of exposure, two in the 30 kDa fragment and one in the 19 kDa fragment. Thus, one sulfhydryl group is cryptic, inaccessible to N-ethylmaleimide in each fragment. In intact cells, the single reactive group of the 19 kDa fragment can be protected against reaction with N-ethylmaleimide by the impermeant sulfhydryl reagent, p-chloromercuribenzene sulfonate (PCMBS). It is, therefore, considered to be exposed on the outer face of the membrane. The two reactive groups of the 30 kDa fragment are not protected by PCMBS and are, therefore, not considered to be exposed to the outside medium. Cytochalasin B, a competitive inhibitor of sugar transport affords temporary protection of the exofacial group of the 19 kDa against reaction with N-ethylmaleimide, and affords longer term protection of one of the reactive groups of the 30 kDa fragment. These findings allow conclusions about the topology of the sugar transport protein in the bilayer. Both proteolytic fragments must cross the bilayer. One of three reactive sulfhydryl groups is exofacial and two may be cytoplasmic. The two cryptic groups may be located within the bilayer.
一种主要包含糖转运蛋白的红细胞膜4.5带蛋白制剂,用巯基试剂N - 乙基[¹⁴C]马来酰亚胺进行标记。在用十二烷基硫酸钠(SDS)变性的制剂中,该肽段(分子量45000至60000)中存在的所有五个巯基在37℃下20分钟内与烷基化剂反应。如果该肽段在脂质小泡中重构,并在用SDS提取和变性之前用胰蛋白酶切割,在一个30 kDa片段中发现三个巯基,在一个19 kDa片段中发现两个巯基。在“天然”重构蛋白中,即使暴露两小时后也只有三个基团反应,其中两个在30 kDa片段中,一个在19 kDa片段中。因此,每个片段中有一个巯基是隐蔽的,不能被N - 乙基马来酰亚胺接近。在完整细胞中,19 kDa片段的单个反应性基团可以被不透膜的巯基试剂对氯汞苯磺酸盐(PCMBS)保护,使其不与N - 乙基马来酰亚胺反应。因此,它被认为暴露在膜的外表面。30 kDa片段的两个反应性基团不受PCMBS保护,因此不被认为暴露于外部介质。细胞松弛素B是糖转运的竞争性抑制剂,它能暂时保护19 kDa片段的外表面基团不与N - 乙基马来酰亚胺反应,并能长期保护30 kDa片段的一个反应性基团。这些发现有助于得出关于糖转运蛋白在双层膜中拓扑结构的结论。两个蛋白水解片段都必须穿过双层膜。三个反应性巯基中的一个是外表面的,两个可能是细胞质的。两个隐蔽基团可能位于双层膜内。