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首页> 外文期刊>Biochimica et Biophysica Acta. Molecular and cell biology of Lipids >Formation of molecular species of mitochondrial cardiolipin 2. A mathematical model of pattern formation by phospholipid transacylation.
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Formation of molecular species of mitochondrial cardiolipin 2. A mathematical model of pattern formation by phospholipid transacylation.

机译:线粒体心磷脂2分子种类的形成。通过磷脂转酰化形成图案的数学模型。

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摘要

Formation of the unique molecular species of mitochondrial cardiolipin requires tafazzin, a transacylase that exchanges acyl groups between phospholipid molecular species without strict specificity for acyl groups, head groups, or carbon positions. However, it is not known whether phospholipid transacylations can cause the accumulation of specific fatty acids in cardiolipin. Here, a model is shown in linear algebra representation, in which acyl specificity emerges from the transacylation equilibrium of multiple molecular species, provided that different species have different free energies. The model defines the conditions and energy terms, under which transacylations may generate the characteristic composition of mitochondrial cardiolipin. It is concluded that acyl-specific cardiolipin patterns could arise from phospholipid transacylations in the tafazzin domain, even if tafazzin itself does not have substrate specificity.
机译:线粒体心磷脂独特分子种类的形成需要tafazzin,它是一种在磷脂分子种类之间交换酰基而对酰基,头基或碳位置没有严格特异性的转酰基转移酶。但是,尚不知道磷脂酰转氨作用是否会引起特定脂肪酸在心磷脂中的积累。在此,以线性代数表示形式显示了一个模型,其中酰基特异性从多种分子物种的转酰基反应平衡中产生,只要不同的物种具有不同的自由能。该模型定义了条件和能量条件,在这些条件和能量条件下,酰化作用可能产生线粒体心磷脂的特征成分。结论是,即使tafazzin本身不具有底物特异性,酰基特异性心磷脂模式也可能由tafazzin域中的磷脂转酰作用引起。

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