Bump N J, Lee J, Wleklik M, Reichler J, Najjar V A
Proc Natl Acad Sci U S A. 1986 Oct;83(19):7187-91. doi: 10.1073/pnas.83.19.7187.
Tuftsin (Thr-Lys-Pro-Arg) receptor was purified to apparent homogeneity by affinity chromatography, using a pentapeptide analog (Thr-Lys-Pro-Pro-Arg) that binds the receptor more than 4 times as avidly as tuftsin. The analog was covalently linked to a solid support (Affi-Gel 10). Rabbit peritoneal granulocyte membrane solubilized with 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate was applied to the affinity column, the column was washed with 0.1 M ammonium carbonate (pH 7.9) and 0.1 M ammonium acetate (pH 5), and bound material was eluted with 20 nM tuftsin or pentapeptide. The eluate was concentrated and subjected to gel filtration; this yielded one major peak of [3H]tuftsin binding activity corresponding to approximately 500 kDa and a minor peak at approximately 250 kDa. Rechromatography of either peak resulted in the appearance of the same major and minor peaks. NaDodSO4/PAGE of the affinity-purified material under nonreducing conditions showed only two silver-staining bands. Electroblotting followed by [3H]tuftsin overlay and fluorography showed two adjacent radioactive bands corresponding in mobility to the silver-stained bands. Under reducing conditions, NaDodSO4/PAGE yielded molecular mass values 62 kDa and 52 kDa for the two tuftsin receptor subunits. Electron microscopy revealed a homogeneous population of spherical molecules with diameters of 104 A.
通过亲和色谱法将促吞噬素(苏氨酸 - 赖氨酸 - 脯氨酸 - 精氨酸)受体纯化至表观均一,使用一种五肽类似物(苏氨酸 - 赖氨酸 - 脯氨酸 - 脯氨酸 - 精氨酸),该类似物与受体的结合亲和力比促吞噬素高4倍以上。该类似物共价连接到固相载体(Affi - Gel 10)上。用3 - [(3 - 胆酰胺丙基)二甲基铵基]-1 - 丙烷磺酸盐溶解的兔腹膜粒细胞膜应用于亲和柱,用0.1M碳酸铵(pH 7.9)和0.1M醋酸铵(pH 5)洗涤该柱,并用20nM促吞噬素或五肽洗脱结合的物质。洗脱液浓缩后进行凝胶过滤;这产生了一个对应于约500kDa的[3H]促吞噬素结合活性的主要峰和一个约250kDa的次要峰。任一峰的再色谱分离都导致出现相同的主要峰和次要峰。在非还原条件下对亲和纯化物质进行的十二烷基硫酸钠/聚丙烯酰胺凝胶电泳(NaDodSO4/PAGE)仅显示两条银染带。随后进行[3H]促吞噬素覆盖和荧光自显影的电印迹显示两条相邻的放射性带,其迁移率与银染带相对应。在还原条件下,NaDodSO4/PAGE给出了促吞噬素受体两个亚基的分子量值分别为62kDa和52kDa。电子显微镜显示直径为104埃的球形分子群体均一。