کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5533217 1402108 2017 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Methods NotesBLaTM 2.0, a Genetic Tool Revealing Preferred Antiparallel Interaction of Transmembrane Helix 4 of the Dual-Topology Protein EmrE
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Methods NotesBLaTM 2.0, a Genetic Tool Revealing Preferred Antiparallel Interaction of Transmembrane Helix 4 of the Dual-Topology Protein EmrE
چکیده انگلیسی


- TMD helix-helix interactions direct the oligomerization and folding of membrane proteins.
- BLaTM 2.0 is a novel genetic tool to measure antiparallel TMD helix interactions.
- The antiparallel interaction of the EmrE TMD4 is much stronger than the parallel one.
- The BLaTM systems allow the comparison of parallel and antiparallel TMD interactions.

Parallel and antiparallel transmembrane helix-helix interactions support the folding and non-covalent assembly of many integral membrane proteins. While several genetic tools are currently in use to study parallel transmembrane helix-helix interactions, antiparallel associations have been difficult to determine. Here, we present a novel genetic approach, termed BLaTM 2.0, which can be used in combination with the recently presented BLaTM 1.2 to compare the efficiency of antiparallel and parallel transmembrane domain (TMD) interactions in a natural membrane. In a practical application of the BLaTM system, we find that the antiparallel interaction of TMD4, the known dimerization domain of the dual-topology small multidrug transporter EmrE, is sequence-specific and much stronger than the parallel one. This suggests that TMD4 has evolved to favor the formation of dual-topology EmrE dimers over single-topology dimers.

Graphical Abstract237

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Biology - Volume 429, Issue 11, 2 June 2017, Pages 1630-1637
نویسندگان
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