Pore-forming proteins;
Protein folding in membrane;
Lipid reorganization;
Proteo-lipidic pore;
STAPHYLOCOCCAL ALPHA-HEMOLYSIN;
BAX-DERIVED PEPTIDE;
EQUINATOXIN-II;
STICHOLYSIN-II;
PERFRINGOLYSIN-O;
MODEL MEMBRANES;
ANTIMICROBIAL PEPTIDES;
CARDIOLIPIN PROVIDES;
CHOLESTEROL-BINDING;
STRUCTURAL BASIS;
D O I:
10.1007/s00232-015-9820-y
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:
Pore-forming proteins (PFPs) punch holes in their target cell membrane to alter their permeability. Permeabilization of lipid membranes by PFPs has received special attention to study the basic molecular mechanisms of protein insertion into membranes and the development of biotechnological tools. PFPs act through a general multi-step mechanism that involves (i) membrane partitioning, (ii) insertion into the hydrophobic core of the bilayer, (iii) oligomerization, and (iv) pore formation. Interestingly, PFPs and membranes show a dynamic interplay. As PFPs are usually produced as soluble proteins, they require a large conformational change for membrane insertion. Moreover, membrane structure is modified upon PFPs insertion. In this context, the toroidal pore model has been proposed to describe a pore architecture in which not only protein molecules but also lipids are directly involved in the structure. Here, we discuss how PFPs and lipids cooperate and remodel each other to achieve pore formation, and explore new evidences of protein-lipid pore structures.
机构:
Univ Calif San Diego, Div Biol Sci, Sect Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol Sci, Sect Cell & Dev Biol, La Jolla, CA 92093 USA
Hu, Yan
Aroian, Raffi V.
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机构:
Univ Calif San Diego, Div Biol Sci, Sect Cell & Dev Biol, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol Sci, Sect Cell & Dev Biol, La Jolla, CA 92093 USA