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发布于:2019-5-16 10:50:14  访问:77 次 回复:0 篇
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Iguration). staggered configuration). Because of this, Hstalks would (partially) dissociate and
However, most recent mechanistic information obtained will not be in direct agreement using the sliding model. Firstly, head/stalk hybrid attachment proteins were reported to preserve F-triggering activity, provided that the stalks along with the F protein originated from the identical virus [139].Iguration). staggered configuration). Because of this, Hstalks PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/20923853 would (partially) dissociate and, in turn, cause the Because of this, H-stalks would (partially) dissociate and, in turn, lead free of charge to undergo the necessary F from disengagement of F from H. Subsequently, F complexes would be towards the disengagement of structural rearrangements to mediate membrane fusion (Figure 4A). H. Subsequently, F complexes would be free of charge to undergo the necessary structural rearrangements to mediate membrane fusion (Figure 4A).Figure four. Models of F activation by paramyxovirus attachment proteins. (A ) Most up-to-date models have Figure four. Models of F activation by paramyxovirus attachment proteins. (A ) Most current models have proposed how attachment protein of various members in the Paramyxovirinae subfamily activates F proposed how attachmentof attachment proteinreceptor binding. Importantly, all models predict a F as a protein of distinct members of the Paramyxovirinae subfamily activates as a consequence consequence of attachment protein-receptor binding. Importantly, all models predict a receptor-induced receptorinduced all round repositioning with the head regions upon receptor engagements, which may all round re-positioning with the head regions upon receptor engagements, which may then act as a then act as a universal core mechanism for F activation (initially described by Bose and colleagues [122]). H tetramers are colored F activation (1st described by Bose and colleagues blue and PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/26344672 tetramers universal core mechanism forin green. Preactivated F and activated F are highlighted in [122]). Hred, respectively. In model (D) (bidentate model) the conformational alterations occurring within the head are colored in green. Pre-activated F and activated F are highlighted in blue and red, respectively. domain prior to heads‘ repositioning are represented by oval structures. The attachment protein stalk In model (D) (bi-dentate model) the conformational alterations occurring within the head domain prior regions which are implicated in F activation are shown as black lines (models B ).to heads‘ re-positioning are represented by oval structures. The attachment protein stalk regions that happen to be implicated in F activation are shown as black lines (models B ). This mechanism infers that MeV Hheads, upon receptor binding, might create particular signalsthat would travel by means of the flexible linkers down towards the stalks for effective F activation. On the other hand, latest mechanistic information obtained are not in direct agreement with the sliding model. Initial of all, head/stalk hybrid attachment proteins have been reported to preserve Ftriggering activity, provided that the stalks and the F protein originated from the identical virus [139]. Contemplating that the entire head/receptor framework is swapped in such chimeric attachment proteins, it really is tricky to think that specific receptorinduced conformational changes could be maintained. Secondly, and mostViruses 2016, 8,13 ofThis mechanism infers that MeV H-heads, upon receptor binding, may well create particular signals that would travel via the versatile linkers down to the stalks for efficient F activation. Even so, newest mechanistic information obtained are usually not in direct agreement (+)-KavainCOA together with the sliding model.
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