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米尔滕贝格III类、IV类和V类人红细胞膜中异常的血型Ss活性唾液糖蛋白。

Abnormal blood-group-Ss-active sialoglycoproteins in the membrane of Miltenberger class III, IV and V human erythrocytes.

作者信息

Anstee D J, Mawby W J, Tanner M J

出版信息

Biochem J. 1979 Nov 1;183(2):193-203. doi: 10.1042/bj1830193.

Abstract
  1. We have studied the inherited changes occurring in the sialoglycoproteins of membranes from erythrocytes of type Miltenberger Class III (Mi.III), Miltenberger Class IV (Mi.IV) and Miltenberger Class V (Mi.V) by using sodium dodecyl sulphate/polyacrylamide gel electrophoresis and lactoperoxidase radioiodination. 2. Mi.III erythrocytes lack the normal blood-group-Ss-active sialoglycoprotein but contain an unusual s-active sialoglycoprotein of higher apparent molecular weight. A similar abnormal S-active sialoglycoprotein appears to occur in Mi.IV erythrocytes. 3. The Mi.V condition is associated with the hemizygous absence of both the normal blood-group-MN-active sialoglycoprotein and the normal Ss-active sialoglycorprotein. However, a new sialoglycoprotein component is present in these cells that has properties characteristic of both the MN-active and Ss-active sialoglycoproteins. 4. Our results suggest that the new sialoglycorportein present in Mi.V erythrocytes is a hybrid of the normal MN sialoglycoprotein and an s-active sialoglycoprotein that has properties similar to the s-active sialoglycoprotein found in Mi.III erythrocytes. We suggest that the unusual Mi.V sialoglycoprotein is derived from chromosomal misalignment with unequal crossing-over between the genes for the MN- and Ss-active sialoglycoproteins in a manner similar to that which gives rise to haemoglobin Lepore. 5. Further studies of S-s-erythrocytes confirm that these cells lack normal Ss-active sialoglycoprotein, but contain an unusual component that shows some of the properties of the normal Ss-active sialoglycoprotein. 6. Analysis of erythrocytes of type Mk/Mi.III confirms that, in addition to the known hemizygous lack of the MN-active sialoglycoprotein, the Mk condition is also associated with a loss of the Ss-active sialoglycoprotein. 7. In order to facilitate discussion of the complex changes that occur in these variant erythrocytes, a new unified nomenclature is used for the erythrocyte sialoglycoproteins.
摘要
  1. 我们通过十二烷基硫酸钠/聚丙烯酰胺凝胶电泳和乳过氧化物酶放射性碘化法,研究了米尔滕贝格III类(Mi.III)、米尔滕贝格IV类(Mi.IV)和米尔滕贝格V类(Mi.V)红细胞膜唾液糖蛋白发生的遗传性变化。2. Mi.III红细胞缺乏正常的血型Ss活性唾液糖蛋白,但含有一种表观分子量较高的异常S活性唾液糖蛋白。类似的异常S活性唾液糖蛋白似乎也存在于Mi.IV红细胞中。3. Mi.V情况与正常血型MN活性唾液糖蛋白和正常Ss活性唾液糖蛋白的半合子缺失有关。然而,这些细胞中存在一种新的唾液糖蛋白成分,它具有MN活性和Ss活性唾液糖蛋白的特征。4. 我们的结果表明,Mi.V红细胞中存在的新唾液糖蛋白是正常MN唾液糖蛋白和一种S活性唾液糖蛋白的杂合体,该S活性唾液糖蛋白的性质与Mi.III红细胞中发现的S活性唾液糖蛋白相似。我们认为,异常的Mi.V唾液糖蛋白是由MN和Ss活性唾液糖蛋白基因之间的染色体错配和不等交换产生的,其方式类似于产生血红蛋白Lepore的方式。5. 对S-s-红细胞的进一步研究证实,这些细胞缺乏正常的Ss活性唾液糖蛋白,但含有一种异常成分,该成分表现出正常Ss活性唾液糖蛋白的一些性质。6. 对Mk/Mi.III型红细胞的分析证实,除了已知的半合子缺乏MN活性唾液糖蛋白外,Mk情况还与Ss活性唾液糖蛋白的缺失有关。7. 为了便于讨论这些变异红细胞中发生的复杂变化,对红细胞唾液糖蛋白采用了一种新的统一命名法。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d908/1161547/abc93a3254e3/biochemj00452-0013-a.jpg

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