In vitro systems in the study of peroxisomal protein import.

Experientia Pub Date : 1996-12-15 DOI:10.1007/BF01952102
A Baker
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引用次数: 3

Abstract

Our level of understanding of peroxisome biogenesis in comparison with other cellular organelles is rudimentary, yet the fragments of information available indicate that the targeting and import of peroxisomal proteins occur by fundamentally different mechanisms. Genetic studies have identified a number of genes required for peroxisome assembly, but in most cases the functions of the gene products remain unknown. In vitro protein translocation systems have played a prominent role in unravelling the biochemistry of protein translocation into other organelles. This review considers some of the requirements for establishing a bona fide peroxisomal import assay and discusses the findings which have emerged as a result of using such experimental systems.

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体外系统中过氧化物酶体蛋白进口的研究。
与其他细胞器相比,我们对过氧化物酶体生物发生的理解水平是初步的,但现有的信息片段表明,过氧化物酶体蛋白的靶向和输入是通过根本不同的机制发生的。遗传学研究已经确定了一些过氧化物酶体组装所需的基因,但在大多数情况下,基因产物的功能仍然未知。在体外,蛋白质易位系统在揭示蛋白质易位到其他细胞器的生物化学过程中发挥了重要作用。本综述考虑了建立真正的过氧化物酶体进口测定的一些要求,并讨论了由于使用这种实验系统而出现的发现。
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Immunogenetics. Cytosolic factors in mitochondrial protein import. Regulated protein degradation in mitochondria. The mitochondrial processing peptidase: function and specificity. Allosteric proteins after thirty years: the binding and state functions of the neuronal alpha 7 nicotinic acetylcholine receptors.
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