Kaldi K, Diestelkötter P, Stenbeck G, Auerbach S, Jäkle U, Mägert H J, Wieland F T, Just W W
Institut für Biochemie I, Universität Heidelberg, Germany.
FEBS Lett. 1993 Jan 11;315(3):217-22. doi: 10.1016/0014-5793(93)81167-x.
In order to study the membrane topology and the possible function of the rat liver 22 kDa integral peroxisomal membrane protein (PMP 22) at a molecular level, we have cloned PMP 22 from a lambda gt11 expression library and sequenced its cDNA. Hydropathy analysis of the deduced primary structure indicates 4 putative transmembrane segments. The accessibility to exogenous aminopeptidase of PMP 22 in intact peroxisomes suggests that the N-terminus faces the cytosol. A model of the topology of PMP 22 in the peroxisomal membrane is discussed. Homology studies revealed a striking similarity with the Mpv 17 gene product. Lack of this membrane protein causes nephrotic syndrome in mice.
为了在分子水平上研究大鼠肝脏22 kDa整合型过氧化物酶体膜蛋白(PMP 22)的膜拓扑结构及其可能的功能,我们从λgt11表达文库中克隆了PMP 22并对其cDNA进行了测序。对推导的一级结构进行亲水性分析表明有4个推定的跨膜区段。完整过氧化物酶体中PMP 22对外源氨肽酶的可及性表明其N端面向细胞质溶胶。讨论了PMP 22在过氧化物酶体膜中的拓扑结构模型。同源性研究显示与Mpv 17基因产物有显著相似性。缺乏这种膜蛋白会导致小鼠出现肾病综合征。