Division of Biophysics, Department of Biology, University of Osnabrück, Barbarastrasse 11, 49076 Osnabrück (Germany) http://www.biophysik.uni-osnabrueck.de.
Angew Chem Int Ed Engl. 2014 Jan 27;53(5):1311-5. doi: 10.1002/anie.201306328. Epub 2013 Dec 18.
Lipid analogues carrying three nitrilotriacetic acid (tris-NTA) head groups were developed for the selective targeting of His-tagged proteins into liquid ordered (lo ) or liquid disordered (ld ) lipid phases. Strong partitioning into the lo phase of His-tagged proteins bound to tris-NTA conjugated to saturated alkyl chains (tris-NTA DODA) was achieved, while tris-NTA conjugated to an unsaturated alkyl chain (tris-NTA SOA) predominantly resided in the ld phase. Interestingly, His-tag-mediated lipid crosslinking turned out to be required for efficient targeting into the lo phase by tris-NTA DODA. Robust partitioning into lo phases was confirmed by using viral lipid mixtures and giant plasma membrane vesicles. Moreover, efficient protein targeting into lo and ld domains within the plasma membrane of living cells was demonstrated by single-molecule tracking, thus establishing a highly generic approach for exploring lipid microdomains in situ.
开发了携带三个氮川三乙酸(tris-NTA)头基的脂质类似物,用于将 His 标记的蛋白质选择性靶向到具有有序(lo)或无序(ld)液晶相的脂质相中。与饱和烷基链(tris-NTA DODA)连接的 tris-NTA 与 His 标记的蛋白质结合后强烈分配到 lo 相中,而与不饱和烷基链(tris-NTA SOA)连接的 tris-NTA 主要位于 ld 相中。有趣的是,His 标记介导的脂质交联对于 tris-NTA DODA 有效地靶向 lo 相是必需的。使用病毒脂质混合物和巨大的质膜囊泡证实了稳健的 lo 相分配。此外,通过单分子追踪证明了在活细胞质膜内的 lo 和 ld 域中蛋白质的有效靶向,从而建立了一种探索原位脂质微区的高度通用方法。