کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1944192 1053188 2014 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Strong dimerization of wild-type ErbB2/Neu transmembrane domain and the oncogenic Val664Glu mutant in mammalian plasma membranes
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Strong dimerization of wild-type ErbB2/Neu transmembrane domain and the oncogenic Val664Glu mutant in mammalian plasma membranes
چکیده انگلیسی


• This is the first quantitative study of ErbB2/Neu TM domain dimerization in mammalian membranes.
• We observe surprisingly strong dimerization propensity of ErbB2/Neu in mammalian membranes.
• The V664E mutation is causing a small, but statistically significant change in dimer structure.
• The results point to a significant role of the TM domain in ErbB2/Neu dimerization and signaling.

Here, we study the homodimerization of the transmembrane domain of Neu, as well as an oncogenic mutant (V664E), in vesicles derived from the plasma membrane of mammalian cells. For the characterization, we use a Förster resonance energy transfer (FRET)-based method termed Quantitative Imaging-FRET (QI-FRET), which yields the donor and acceptor concentrations in addition to the FRET efficiencies in individual plasma membrane-derived vesicles. Our results demonstrate that both the wild-type and the mutant are 100% dimeric, suggesting that the Neu TM helix dimerizes more efficiently than other RTK TM domains in mammalian membranes. Furthermore, the data suggest that the V664E mutation causes a very small, but statistically significant change in dimer structure. This article is part of a Special Issue entitled: Interfacially Active Peptides and Proteins. Guest Editors: William C. Wimley and Kalina Hristova.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Biomembranes - Volume 1838, Issue 9, September 2014, Pages 2326–2330
نویسندگان
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