Fransen M, Terlecky S R, Subramani S
Department of Biology, University of California at San Diego, La Jolla, CA 92093-0322, USA.
Proc Natl Acad Sci U S A. 1998 Jul 7;95(14):8087-92. doi: 10.1073/pnas.95.14.8087.
The discovery of many fatal human disorders resulting from impaired peroxisomal protein import makes the functional characterization of human peroxins critical. As part of our attempt to identify novel human genes and gene products involved in the import of peroxisomal proteins, we raised antisera against peroxisomal membrane proteins. One such antiserum inhibited peroxisomal protein import in semipermeabilized mammalian cells. This "import inhibiting" antiserum, ab-MF3, specifically recognized a 57-kDa protein. Immunoblot analysis of rat liver subcellular fractions demonstrated that this protein was present exclusively in peroxisomal membranes. Functional analysis revealed that this 57-kDa molecule bound the PTS1 receptor, Pex5p, in ligand blots, suggesting it is a docking site on the peroxisomal membrane. Previous studies have identified two yeast proteins, Pex14p and Pex13p, as Pex5p-binding proteins. To facilitate the biochemical analysis of peroxisomal membrane docking proteins, we cloned and expressed the previously unidentified human Pex14p, as well as a human Pex13p that is 39 aa longer than previously reported. Recombinant Pex14p was specifically recognized by the "import inhibiting" ab-MF3 and bound Pex5p and the Src homology 3 (SH3) domain of Pex13p in ligand blots. These studies demonstrate that the ab-MF3-immunoreactive, 57-kDa peroxisomal membrane protein is Pex14p. Furthermore, this peroxin interacts with Pex5p and Pex13p(SH3) and is directly required for peroxisomal protein import.
许多因过氧化物酶体蛋白输入受损而导致的致命人类疾病的发现,使得对人类过氧化物酶进行功能表征变得至关重要。作为我们识别参与过氧化物酶体蛋白输入的新型人类基因和基因产物的尝试的一部分,我们制备了针对过氧化物酶体膜蛋白的抗血清。一种这样的抗血清抑制了半透性哺乳动物细胞中的过氧化物酶体蛋白输入。这种“输入抑制”抗血清,即ab-MF3,特异性识别一种57 kDa的蛋白质。对大鼠肝脏亚细胞组分的免疫印迹分析表明,这种蛋白质仅存在于过氧化物酶体膜中。功能分析显示,这个57 kDa的分子在配体印迹中与过氧化物酶体靶向信号1(PTS1)受体Pex5p结合,表明它是过氧化物酶体膜上的一个停靠位点。先前的研究已经鉴定出两种酵母蛋白Pex14p和Pex13p为Pex5p结合蛋白。为了便于对过氧化物酶体膜停靠蛋白进行生化分析,我们克隆并表达了之前未鉴定的人类Pex14p,以及一种比先前报道的长39个氨基酸的人类Pex13p。重组Pex14p在配体印迹中被“输入抑制”的ab-MF3特异性识别,并与Pex5p和Pex13p的Src同源3(SH3)结构域结合。这些研究表明,ab-MF3免疫反应性的57 kDa过氧化物酶体膜蛋白是Pex14p。此外,这种过氧化物酶与Pex5p和Pex13p(SH3)相互作用,并且是过氧化物酶体蛋白输入直接所需的。