Distance Regulated Vesicle Fusion and Docking Mediated by -Peptide Nucleic Acid SNARE Protein Analogues

被引:17
|
作者
Sadek, Muheeb [1 ]
Berndt, Daniel [1 ]
Milovanovic, Dragomir [2 ]
Jahn, Reinhard [2 ]
Diederichsen, Ulf [1 ]
机构
[1] Univ Gottingen, Inst Organ & Biomol Chem, Tammannstr 2, D-370770 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Abt Neurobiol, Fassberg 11, D-37077 Gottingen, Germany
关键词
beta-peptide; membranes; protein-protein interactions; SNARE proteins; transmembrane domains; vesicles; ANTIMICROBIAL BETA-PEPTIDES; HELICAL SECONDARY STRUCTURE; DE-NOVO DESIGN; MEMBRANE-FUSION; SIDE-CHAINS; UNILAMELLAR VESICLES; RECOGNITION; PRINCIPLES; FOLDAMERS; SEQUENCES;
D O I
10.1002/cbic.201500517
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Artificial SNARE analogues derived from SNARE proteins, which mediate synaptic membrane fusion, are of interest. They mimic the tetrameric -helix bundle of the SNARE motif with various bio-oligomer recognition units. Interaction between complementary oligomers linked to the respective membrane by lipid or peptide anchors leads to proximity of vesicles and to fusion of lipid bilayers. -Peptide nucleic acids were introduced as hybrid oligomers with the native SNARE protein transmembrane/linker sequence, in order to evaluate a fusion system that allows distance tuning of approaching membranes. Formation of a four-base pair -PNA double strand with 20 angstrom length is sufficient for vesicle membrane fusion. Elongation of the recognition -PNA duplex in the linker region yielded a 40 angstrom -peptide duplex and provided a vesicle-vesicle distance that only supported hemifusion of vesicle membranes.
引用
收藏
页码:479 / 485
页数:7
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