Basic amino acids in a distinct subset of signal peptides promote interaction with the signal recognition particle

被引:66
作者
Peterson, JH [1 ]
Woolhead, CA [1 ]
Bernstein, HD [1 ]
机构
[1] NIDDK, Genet & Biochem Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1074/jbc.M309082200
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
Previous studies have demonstrated that signal peptides bind to the signal recognition particle (SRP) primarily via hydrophobic interactions with the 54-kDa protein subunit. The crystal structure of the conserved SRP ribonucleoprotein core, however, raised the surprising possibility that electrostatic interactions between basic amino acids in signal peptides and the phosphate backbone of SRP RNA may also play a role in signal sequence recognition. To test this possibility we examined the degree to which basic amino acids in a signal peptide influence the targeting of two Escherichia coli proteins, maltose binding protein and OmpA. Whereas both proteins are normally targeted to the inner membrane by SecB, we found that replacement of their native signal peptides with another moderately hydrophobic but unusually basic signal peptide (DeltaEspP) rerouted them into the SRP pathway. Reduction in either the net positive charge or the hydrophobicity of the DeltaEspP signal peptide decreased the effectiveness of SRP recognition. A high degree of hydrophobicity, however, compensated for the loss of basic residues and restored SRP binding. Taken together, the data suggest that the formation of salt bridges between SRP RNA and basic amino acids facilitates the binding of a distinct subset of signal peptides whose hydrophobicity falls slightly below a threshold level.
引用
收藏
页码:46155 / 46162
页数:8
相关论文
共 39 条
[21]  
LESLEY SA, 1991, J BIOL CHEM, V266, P2632
[22]   Evidence for a novel GTPase priming step in the SRP protein targeting pathway [J].
Lu, Y ;
Qi, HY ;
Hyndman, JB ;
Ulbrandt, ND ;
Teplyakov, A ;
Tomasevic, N ;
Bernstein, HD .
EMBO JOURNAL, 2001, 20 (23) :6724-6734
[23]   SECRETORY PROTEIN TRANSLOCATION ACROSS MEMBRANES - THE ROLE OF THE DOCKING PROTEIN [J].
MEYER, DI ;
KRAUSE, E ;
DOBBERSTEIN, B .
NATURE, 1982, 297 (5868) :647-650
[24]   GTP-BINDING AND HYDROLYSIS BY THE SIGNAL RECOGNITION PARTICLE DURING INITIATION OF PROTEIN TRANSLOCATION [J].
MILLER, JD ;
WILHELM, H ;
GIERASCH, L ;
GILMORE, R ;
WALTER, P .
NATURE, 1993, 366 (6453) :351-354
[25]   Signal sequences specify the targeting route to the endoplasmic reticulum membrane [J].
Ng, DTW ;
Brown, JD ;
Walter, P .
JOURNAL OF CELL BIOLOGY, 1996, 134 (02) :269-278
[26]  
NOTHWEHR SF, 1990, J BIOL CHEM, V265, P17202
[27]   Functional analysis of the signal recognition particle in Escherichia coli by characterization of a temperature-sensitive ffh mutant [J].
Park, SK ;
Jiang, FL ;
Dalbey, RE ;
Phillips, GJ .
JOURNAL OF BACTERIOLOGY, 2002, 184 (10) :2642-2653
[28]   AN ESCHERICHIA-COLI RIBONUCLEOPROTEIN CONTAINING 4.5S RNA RESEMBLES MAMMALIAN SIGNAL RECOGNITION PARTICLE [J].
PORITZ, MA ;
BERNSTEIN, HD ;
STRUB, K ;
ZOPF, D ;
WILHELM, H ;
WALTER, P .
SCIENCE, 1990, 250 (4984) :1111-1117
[29]   CORRELATION OF COMPETENCE FOR EXPORT WITH LACK OF TERTIARY STRUCTURE OF THE MATURE SPECIES - A STUDY INVIVO OF MALTOSE-BINDING PROTEIN IN ESCHERICHIA-COLI [J].
RANDALL, LL ;
HARDY, SJS .
CELL, 1986, 46 (06) :921-928
[30]   FUNCTIONS OF SIGNAL AND SIGNAL ANCHOR SEQUENCES ARE DETERMINED BY THE BALANCE BETWEEN THE HYDROPHOBIC SEGMENT AND THE N-TERMINAL CHARGE [J].
SAKAGUCHI, M ;
TOMIYOSHI, R ;
KUROIWA, T ;
MIHARA, K ;
OMURA, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (01) :16-19