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Studies on human porin: XIII. The type‐1 VDAC ‘Porin 31HL’ biotinylated at the plasmalemma of Trypan blue excluding human B lymphocytes

Christian JakobMax-Planck-Institut für experimentelle Medizin, Abt. Immunchemie, Göttingen, GermanyHilde GötzMax-Planck-Institut für experimentelle Medizin, Abt. Immunchemie, Hermann-Rein Str.3, D-37075 Göttingen, GermanyThea HellmannMax-Planck-Institut für experimentelle Medizin, Abt. Immunchemie, Hermann-Rein Str.3, D-37075 Göttingen, GermanyKlaus P. HellmannMax-Planck-Institut für experimentelle Medizin, Abt. Immunchemie, Hermann-Rein Str.3, D-37075 Göttingen, GermanySusanne ReymannMax-Planck-Institut für experimentelle Medizin, Abt. Immunchemie, Hermann-Rein Str.3, D-37075 Göttingen, GermanyHarald FlörkeMax-Planck-Institut für experimentelle Medizin, Abt. Immunchemie, Hermann-Rein Str.3, D-37075 Göttingen, GermanyFriedrich P. ThinnesMax-Planck-Institut für experimentelle Medizin, Abt. Immunchemie, Hermann-Rein Str.3, D-37075 Göttingen, GermanyN HilschmannMax-Planck-Institut für experimentelle Medizin, Abt. Immunchemie, Hermann-Rein Str.3, D-37075 Göttingen, Germany
1995en
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In 1989, we demonstrated for the first time the expression of the VDAC 'Porin 31HL' in the plasmalemma of human B lymphocytes, then giving first evidence of a multi-topological expression of VDAC. Meanwhile, data from this and other laboratories support our proposal of a multi-compartment distribution of the channel in mammalian tissues. Here, by biotinylation of plasmalemma-integrated proteins of proven living B lymphocytes, followed by two-dimensional electrophoresis, immuno- and streptavidin affinity blotting, we show that part of the channel molecules can be labelled at the outer membrane of the cells. Thus, by a relevant approach our results invalidate objections concerning putative cross-reactivity of anti-human Type-1 porin antibodies with non-VDAC proteins at the outer cell membrane.

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