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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
来源:
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.
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页码:479 / 485
页数:7
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