Becker K, Guiard B, Rassow J, Söllner T, Pfanner N
Institut für Physiologische Chemie, Universität München, Federal Republic of Germany.
J Biol Chem. 1992 Mar 15;267(8):5637-43.
To analyze the role of cytosolic cofactors in mitochondrial protein targeting, we prepared a chemically pure mitochondrial preprotein. When diluted out of 7 M urea, this precursor protein was efficiently imported into mitochondria without the addition of cytosolic cofactors. Extensive prewashing of mitochondria (up to 2 M KCl) did not reduce its import. Import of the purified precursor showed the characteristics of authentic mitochondrial import including use of the receptor MOM19, requirement for a membrane potential, and proteolytic processing. When the precursor was preincubated at a low concentration of urea, cytosolic cofactors were needed to preserve its import competence. We conclude that targeting of this preprotein via the mitochondrial master receptor MOM19 does not require a cytosolic signal recognition factor; cytosolic cofactors apparently have chaperone-like functions in mitochondrial protein uptake. Moreover, we found that a cleavable presequence was sufficient to direct protein import via MOM19. Together with the cofactor-independent function of MOM19, it is thus conceivable that MOM19 functions as mitochondrial presequence receptor.
为了分析胞质辅因子在线粒体蛋白靶向中的作用,我们制备了一种化学纯的线粒体前体蛋白。当从7M尿素中稀释出来时,这种前体蛋白无需添加胞质辅因子就能高效地导入线粒体。对线粒体进行大量预洗涤(高达2M KCl)并不会降低其导入效率。纯化前体的导入显示出真正线粒体导入的特征,包括使用受体MOM19、对膜电位的需求以及蛋白水解加工。当前体在低浓度尿素中预孵育时,需要胞质辅因子来维持其导入能力。我们得出结论,通过线粒体主要受体MOM19对这种前体蛋白进行靶向不需要胞质信号识别因子;胞质辅因子显然在线粒体蛋白摄取中具有类似伴侣的功能。此外,我们发现一个可裂解的前导序列足以通过MOM19指导蛋白导入。因此,结合MOM19的辅因子非依赖性功能,可以设想MOM19作为线粒体前导序列受体发挥作用。