Lentil lectin enriched microsomes from the plasma membrane of the human B-lymphocyte cell line H2LCL carry a heavy load of type-1 porin

被引:15
作者
Eben-Brunnen, J
Reymann, S
Awni, LA
Cole, T
Hellmann, T
Hellmann, KP
Paetzold, G
Kleineke, J
Thinnes, FP
Götz, H
Hilschmann, N
机构
[1] Max Planck Inst Expt Med, Dept Immunichem, D-37075 Gottingen, Germany
[2] Max Planck Inst Expt Med, Electron Microscopy Lab, D-37075 Gottingen, Germany
[3] Univ Gottingen, Dept Clin Biochem, Div Internal Med, D-37075 Gottingen, Germany
关键词
affinity chromatography; Lens culinaris; voltage-dependent anion channel; volume regulation;
D O I
10.1515/bchm.1998.379.12.1419
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Using an established biochemical approach, five subcellular fractions of human B lymphocytes were prepared by differential centrifugation. Crude membranes were passed over a lentil lectin column to enrich carbohydrate-coated cell surface microsomes. The lectin-bound fraction contained a high amount of plasma membrane-derived microsomes as indicated by cell surface markers. All subcellular fractions in Western blots proved to contain distinct but variable amounts of porin. There was a strong increase in porin content from crude membranes to plasma membrane-derived vesicles. The porin content of this fraction appeared to be higher than that of mitochondria. In the final step the plasma membrane-derived microsome fraction proved to be devoid of contamination by outer mitochondrial membranes, as revealed by antibodies against the established markers MAO B and Tom20 applied in Western blots. These data prove the extramitochondrial expression of human type-1 porin/type-1 VDAC.
引用
收藏
页码:1419 / 1426
页数:8
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