Protein secretion is an essential cellular process. Signal sequences, RNA-containing targeting factors (Signal Recognition Particle, SRP), and a translocation machinery that contains a heterotrimeric complex o membrane proteins have been discovered in all three domains of life. In Escherichia coli, signal sequences are found on proteins destined for the inner or outer membranes, the periplasmic space located between these lipid bilayers, and on proteins that are secreted into the growth media. The prokaryotic SEP (pSRP) containsa protein, Ffh and 4.5S RNA, and the heterotrimeric membrane protein complex is comprised of SecY (PrlA), SecE (PrlG), and SecG (PrlH). Secretory components that are unique to bacteria include the secretion specific chaperone, SecB, and a translocation ATPase, SecA (PrlD). The prl alleles of the various sec genes are suppressor mutations that restore the secretion o: preproteins with defective signal sequences. We have shown that PrlA and PrlG act by abolishing a signal sequence proofreading function, and we will test our hypothesis that signal sequences interact directly with transmembrane helix 7 of SecY. In vivo crosslinking of SecY and SecE by disulfide bonding, and depletion of Ffh cause similar phenotypes. We will test whether this indicates a more fundamental role for pSRP. We will also explore the possibility that a novel mutation,prlFl, affects a targeting activity of SecYEG for inner membrane proteins. We have discovered partially overlapping signal transduction pathways (Cpx and aE) that control the synthesis of periplasmic protein folding factors and a protease. We will continue our search for additiona factors and we will investigate how these molecules function in outer membrane biogenesis. In addition, we will determinethe mechanism by which the histidinekinase CpxA senses envelope stress, and we will test our prediction that Cpx is the master regulator of the """"""""attached"""""""" phase during urinary tract infection. Results o: these studies may suggest new ways to treat or prevent certain types of bacterial infections.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37GM034821-23
Application #
7219532
Study Section
Special Emphasis Panel (NSS)
Program Officer
Shapiro, Bert I
Project Start
1985-04-01
Project End
2009-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
23
Fiscal Year
2007
Total Cost
$617,099
Indirect Cost
Name
Princeton University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
002484665
City
Princeton
State
NJ
Country
United States
Zip Code
08544
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Sutterlin, Holly A; Shi, Handuo; May, Kerrie L et al. (2016) Disruption of lipid homeostasis in the Gram-negative cell envelope activates a novel cell death pathway. Proc Natl Acad Sci U S A 113:E1565-74
Lee, James; Xue, Mingyu; Wzorek, Joseph S et al. (2016) Characterization of a stalled complex on the ?-barrel assembly machine. Proc Natl Acad Sci U S A 113:8717-22

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