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21.
Mechanical properties of biological membranes are known to regulate membrane protein function. Despite this, current models of protein communication typically feature only direct protein-protein or protein-small molecule interactions. Here we show for the first time that, by harnessing nanoscale mechanical energy within biological membranes, it is possible to promote controlled communication between proteins. By coupling lipid-protein modules and matching their response to the mechanical properties of the membrane, we have shown that the action of phospholipase A(2) on acyl-based phospholipids triggers the opening of the mechanosensitive channel, MscL, by generating membrane asymmetry. Our findings confirm that the global physical properties of biological membranes can act as information pathways between proteins, a novel mechanism of membrane-mediated protein-protein communication that has important implications for (i) the underlying structure of signaling pathways, (ii) our understanding of in vivo communication networks, and (iii) the generation of building blocks for artificial protein networks.  相似文献   
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Uncountable Cofinalities of Permutation Groups   总被引:2,自引:0,他引:2  
A sufficient criterion is found for certain permutation groupsG to have uncountable strong cofinality, that is, they cannotbe expressed as the union of a countable, ascending chain (Hi)i  相似文献   
24.
It is shown that each group is the outer automorphism groupof a simple group. Surprisingly, the proof is mainly based onthe theory of ordered or relational structures and their symmetrygroups. By a recent result of Droste and Shelah, any group isthe outer automorphism group Out (Aut T) of the automorphismgroup Aut T of a doubly homogeneous chain (T, ). However, AutT is never simple. Following recent investigations on automorphismgroups of circles, it is possible to turn (T, ) into a circleC such that Out (Aut T) Out (Aut C). The unavoidable normalsubgroups in Aut T evaporate in Aut C, which is now simple,and the result follows.  相似文献   
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