Eukaryotic cells are characterized by numerous membrane-bounded compartments that perform specialized functions essential for the cell. Protein targeting and translocation systems maintain the proper composition of these compartments. Mis-targeting of proteins can lead to disease. Examples of this are I-cell and hyperoxaluria I, where enzymes are localized to the wrong compartment. The long range goal of our research is to understand the molecular basis and biochemical mechanisms of a variety of targeting and translocation systems. The investigator's are particularly interested in the evolution of translocation systems to accommodate assembly requirements of their substrates. Eukaryotic cells consist of protein import systems and protein export systems. The latter derive from systems present in the bacterial cell membrane. During the last two years, two new export systems have been described. One, called the Delta pH system, was originally discovered in the thylakoied membrane of chloroplasts, but appears to be widely present in prokaryotes and also in eukaryotic organelles. The Delta pH system specifically transports a subset of proteins to the lumen in parallel with the well-studied SecA/SecY system. The identified components of the Delta pH system are unlike those of the Sec system. The proposed work aims to determine the basis for the existence of these two parallel systems and to elucidate the mechanisms by which the Delta pH system recognizes and transports it proteins. The first specific aim is to determine if the Delta pH system can transport folded proteins and if substrates of the Delta pH system need to be folded during transport. The second specific aim is to investigate the mechanism of the Delta pH system by characterizing two intermediates of the pathway. Finally, they propose experiments to develop in vitro and in vivo assays that will examine the functions and the functional motifs of components of the Delta pH system. Genetic studies have revealed the in vivo necessity of multiple protein transport systems in a number of cell membranes. Therefore, results of the proposed studies will be generally applicable and relevant to basic cell biology and human health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM046951-12
Application #
6636043
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Shapiro, Bert I
Project Start
1992-02-01
Project End
2004-02-29
Budget Start
2003-03-01
Budget End
2004-02-29
Support Year
12
Fiscal Year
2003
Total Cost
$156,143
Indirect Cost
Name
University of Florida
Department
Miscellaneous
Type
Schools of Earth Sciences/Natur
DUNS #
969663814
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Aldridge, Cassie; Ma, Xianyue; Gerard, Fabien et al. (2014) Substrate-gated docking of pore subunit Tha4 in the TatC cavity initiates Tat translocase assembly. J Cell Biol 205:51-65
Ma, Xianyue; Cline, Kenneth (2013) Mapping the signal peptide binding and oligomer contact sites of the core subunit of the pea twin arginine protein translocase. Plant Cell 25:999-1015
Celedon, Jose M; Cline, Kenneth (2013) Intra-plastid protein trafficking: how plant cells adapted prokaryotic mechanisms to the eukaryotic condition. Biochim Biophys Acta 1833:341-51
Celedon, Jose M; Cline, Kenneth (2012) Stoichiometry for binding and transport by the twin arginine translocation system. J Cell Biol 197:523-34
Aldridge, Cassie; Storm, Amanda; Cline, Kenneth et al. (2012) The chloroplast twin arginine transport (Tat) component, Tha4, undergoes conformational changes leading to Tat protein transport. J Biol Chem 287:34752-63
Skalitzky, Courtney A; Martin, Jonathan R; Harwood, Jessica H et al. (2011) Plastids contain a second sec translocase system with essential functions. Plant Physiol 155:354-69
Rodrigues, Ricardo A O; Silva-Filho, Marcio C; Cline, Kenneth (2011) FtsH2 and FtsH5: two homologous subunits use different integration mechanisms leading to the same thylakoid multimeric complex. Plant J 65:600-9
Colquhoun, Thomas A; Schimmel, Bernardus C J; Kim, Joo Young et al. (2010) A petunia chorismate mutase specialized for the production of floral volatiles. Plant J 61:145-55
Ma, Xianyue; Cline, Kenneth (2010) Multiple precursor proteins bind individual Tat receptor complexes and are collectively transported. EMBO J 29:1477-88
Martin, Jonathan R; Harwood, Jessica H; McCaffery, Michael et al. (2009) Localization and integration of thylakoid protein translocase subunit cpTatC. Plant J 58:831-42

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