TY - JOUR
T1 - Membrane Binding of Ribosomes Occurs at SecYE-based Sites in the Archaea Haloferax volcanii
AU - Ring, Gabriela
AU - Eichler, Jerry
N1 - Funding Information:
The authors thank Miriam Laschover (Weizmann Institute of Science) for her advice on ribosome preparation, and Professor Ada Yonath (Weizmann Institute of Science) for gifts of anti-L11 and anti-L12 antibodies. This work was supported by the Israel Science Foundation.
PY - 2004/3/5
Y1 - 2004/3/5
N2 - Whereas ribosomes bind to membranes at eukaryal Sec61αβγ and bacterial SecYEG sites, ribosomal membrane binding has yet to be studied in Archaea. Accordingly, functional ribosomes and inverted membrane vesicles were prepared from the halophilic archaea Haloferax volcanii. The ability of the ribosomes to bind to the membranes was determined using a flotation approach. Proteolytic pretreatment of the vesicles, as well as quantitative analyses, revealed the existence of a proteinaceous ribosome receptor, with the affinity of binding being comparable to that found in Eukarya and Bacteria. Inverted membrane vesicles prepared from cells expressing chimeras of SecE or SecY fused to a cytoplasmically oriented cellulose-binding domain displayed reduced ribosome binding due to steric hindrance. Pretreatment with cellulose drastically reduced ribosome binding to chimera-containing but not wild-type vesicles. Thus, as in Eukarya and Bacteria, ribosome binding in Archaea occurs at Sec-based sites. However, unlike the situation in the other domains of Life, ribosome binding in haloarchaea requires molar concentrations of salt. Structural information on ribosome-Sec complexes may provide insight into this high salt-dependent binding.
AB - Whereas ribosomes bind to membranes at eukaryal Sec61αβγ and bacterial SecYEG sites, ribosomal membrane binding has yet to be studied in Archaea. Accordingly, functional ribosomes and inverted membrane vesicles were prepared from the halophilic archaea Haloferax volcanii. The ability of the ribosomes to bind to the membranes was determined using a flotation approach. Proteolytic pretreatment of the vesicles, as well as quantitative analyses, revealed the existence of a proteinaceous ribosome receptor, with the affinity of binding being comparable to that found in Eukarya and Bacteria. Inverted membrane vesicles prepared from cells expressing chimeras of SecE or SecY fused to a cytoplasmically oriented cellulose-binding domain displayed reduced ribosome binding due to steric hindrance. Pretreatment with cellulose drastically reduced ribosome binding to chimera-containing but not wild-type vesicles. Thus, as in Eukarya and Bacteria, ribosome binding in Archaea occurs at Sec-based sites. However, unlike the situation in the other domains of Life, ribosome binding in haloarchaea requires molar concentrations of salt. Structural information on ribosome-Sec complexes may provide insight into this high salt-dependent binding.
KW - Archaea
KW - Halophiles
KW - Protein translocation
KW - Ribosomes
KW - Translocon
UR - http://www.scopus.com/inward/record.url?scp=1242272089&partnerID=8YFLogxK
U2 - 10.1016/j.jmb.2004.01.008
DO - 10.1016/j.jmb.2004.01.008
M3 - Article
AN - SCOPUS:1242272089
SN - 0022-2836
VL - 336
SP - 997
EP - 1010
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 5
ER -