ASSEMBLY OF THE PREPROTEIN RECEPTOR MOM72/MAS70 INTO THE PROTEIN IMPORT COMPLEX OF THE OUTER-MEMBRANE OF MITOCHONDRIA

被引:34
作者
SCHLOSSMANN, J [1 ]
NEUPERT, W [1 ]
机构
[1] UNIV MUNICH,INST PHYSIOL CHEM,D-80336 MUNICH,GERMANY
关键词
D O I
10.1074/jbc.270.45.27116
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane integration and assembly of MOM72 from Neurospora crassa and its yeast homolog MAS70 was studied with isolated mitochondria. After synthesis in vitro, the precursors of MOM72/MAS70 are tightly folded and expose only their N-terminal amino acid residues comprising the targeting and the membrane anchor domain. Insertion of the protein into the mitochondrial outer membrane (MOM) occurs in a time- and temperature-dependent manner and is stimulated by ATP. MOM72/MAS70 is then assembled into the outer membrane MOM complex. Whereas membrane insertion occurred independently of the presence of protease-sensitive surface components, the assembly reaction depended on such components. In the MOM complex MOM72 and MAS70 were found in the neighborhood of different components in yeast and N. crassa mitochondria, MOM72 was found in association with MOM22 in N. crassa mitochondria, whereas MAS70 was in proximity to a 37-kDa component in yeast outer mitochondrial membrane. The interaction with the 37-kDa protein is important for integration of MAS70 into the MOM complex. Thus, the 37-kDa protein plays an important role in the biogenesis of MAS70.
引用
收藏
页码:27116 / 27121
页数:6
相关论文
共 43 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   THE PURIFIED ESCHERICHIA-COLI INTEGRAL MEMBRANE-PROTEIN SECY/E IS SUFFICIENT FOR RECONSTITUTION OF SECA-DEPENDENT PRECURSOR PROTEIN TRANSLOCATION [J].
BRUNDAGE, L ;
HENDRICK, JP ;
SCHIEBEL, E ;
DRIESSEN, AJM ;
WICKNER, W .
CELL, 1990, 62 (04) :649-657
[3]   YDJ1P FACILITATES POLYPEPTIDE TRANSLOCATION ACROSS DIFFERENT INTRACELLULAR MEMBRANES BY A CONSERVED MECHANISM [J].
CAPLAN, AJ ;
CYR, DM ;
DOUGLAS, MG .
CELL, 1992, 71 (07) :1143-1155
[4]  
DAUM G, 1982, J BIOL CHEM, V257, P3028
[5]   A SUBFAMILY OF STRESS PROTEINS FACILITATES TRANSLOCATION OF SECRETORY AND MITOCHONDRIAL PRECURSOR POLYPEPTIDES [J].
DESHAIES, RJ ;
KOCH, BD ;
WERNERWASHBURNE, M ;
CRAIG, EA ;
SCHEKMAN, R .
NATURE, 1988, 332 (6167) :800-805
[6]   MAS37P, A NOVEL RECEPTOR SUBUNIT FOR PROTEIN IMPORT INTO MITOCHONDRIA [J].
GRATZER, S ;
LITHGOW, T ;
BAUER, RE ;
LAMPING, E ;
PALTAUF, F ;
KOHLWEIN, SD ;
HAUCKE, V ;
JUNNE, T ;
SCHATZ, G ;
HORST, M .
JOURNAL OF CELL BIOLOGY, 1995, 129 (01) :25-34
[7]   A CRUCIAL ROLE OF THE MITOCHONDRIAL PROTEIN IMPORT RECEPTOR MOM19 FOR THE BIOGENESIS OF MITOCHONDRIA [J].
HARKNESS, TAA ;
NARGANG, FE ;
VANDERKLEI, I ;
NEUPERT, W ;
LILL, R .
JOURNAL OF CELL BIOLOGY, 1994, 124 (05) :637-648
[8]  
HARKNESS TAA, 1994, GENETICS, V136, P107
[9]  
HASHIYA N, 1994, EMBO J, V13, P5146
[10]   PROTEIN IMPORT INTO YEAST MITOCHONDRIA IS ACCELERATED BY THE OUTER-MEMBRANE PROTEIN MAS70 [J].
HINES, V ;
BRANDT, A ;
GRIFFITHS, G ;
HORSTMANN, H ;
BRUTSCH, H ;
SCHATZ, G .
EMBO JOURNAL, 1990, 9 (10) :3191-3200