کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1944192 | 1053188 | 2014 | 5 صفحه PDF | دانلود رایگان |

• 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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Journal: Biochimica et Biophysica Acta (BBA) - Biomembranes - Volume 1838, Issue 9, September 2014, Pages 2326–2330