Abstract:
:We report the crystal structure of a bromide-bound form of the D85S mutant of bacteriorhodopsin, bR(D85S), a protein that uses light energy rather than ATP to pump halide ions across the cell membrane. Comparison of the structure of the halide-bound and halide-free states reveals that both displacements of individual side-chain positions and concerted helical movements occur on the extracellular side of the protein. Analysis of these structural changes reveals how this ion pump first facilitates ion uptake deep within the cell membrane and then prevents the backward escape of ions later in the pumping cycle. Together with the information provided by structures of intermediate states in the bacteriorhodopsin photocycle, this study also suggests the overall design principles that are necessary for ion pumping.
journal_name
Biophys Jjournal_title
Biophysical journalauthors
Facciotti MT,Cheung VS,Nguyen D,Rouhani S,Glaeser RMdoi
10.1016/S0006-3495(03)74490-7subject
Has Abstractpub_date
2003-07-01 00:00:00pages
451-8issue
1eissn
0006-3495issn
1542-0086pii
S0006-3495(03)74490-7journal_volume
85pub_type
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