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1.
Biosens Bioelectron ; 36(1): 230-5, 2012.
Article in English | MEDLINE | ID: mdl-22565093

ABSTRACT

Biological environmental monitoring (BEM) is a growing field of research which challenges both microfluidics and system automation. The aim is to develop a transportable system with analysis throughput which satisfies the requirements: (i) fully autonomous, (ii) complete protocol integration from sample collection to final analysis, (iii) detection of diluted molecules or biological species in a large real life environmental sample volume, (iv) robustness and (v) flexibility and versatility. This paper discusses all these specifications in order to define an original fluidic architecture based on three connected modules, a sampling module, a sample preparation module and a detection module. The sample preparation module highly concentrates on the pathogens present in a few mL samples of complex and unknown solutions and purifies the pathogens' nucleic acids into a few µL of a controlled buffer. To do so, a two-step concentration protocol based on magnetic beads is automated in a reusable macro-to-micro fluidic system. The detection module is a PCR based miniaturized platform using digital microfluidics, where reactions are performed in 64 nL droplets handled by electrowetting on dielectric (EWOD) actuation. The design and manufacture of the two modules are reported as well as their respective performances. To demonstrate the integration of the complete protocol in the same system, first results of pathogen detection are shown.


Subject(s)
DNA/analysis , Environmental Monitoring/methods , Microfluidic Analytical Techniques/instrumentation , Microfluidic Analytical Techniques/methods , Adenoviruses, Human/isolation & purification , Bacillus subtilis/isolation & purification , Baculoviridae/isolation & purification , Escherichia coli/isolation & purification , Humans , Polymerase Chain Reaction/methods , Sensitivity and Specificity , Streptococcus pneumoniae/isolation & purification
2.
Proc Natl Acad Sci U S A ; 104(19): 7803-8, 2007 May 08.
Article in English | MEDLINE | ID: mdl-17470796

ABSTRACT

Type III secretion systems (T3SS), found in several Gram-negative pathogens, are nanomachines involved in the transport of virulence effectors directly into the cytoplasm of target cells. T3SS are essentially composed of basal membrane-embedded ring-like structures and a hollow needle formed by a single polymerized protein. Within the bacterial cytoplasm, the T3SS needle protein requires two distinct chaperones for stabilization before its secretion, without which the entire T3SS is nonfunctional. The 2.0-A x-ray crystal structure of the PscE-PscF(55-85)-PscG heterotrimeric complex from Pseudomonas aeruginosa reveals that the C terminus of the needle protein PscF is engulfed within the hydrophobic groove of the tetratricopeptide-like molecule PscG, indicating that the macromolecular scaffold necessary to stabilize the T3SS needle is totally distinct from chaperoned complexes between pilus- or flagellum-forming molecules. Disruption of specific PscG-PscF interactions leads to impairment of bacterial cytotoxicity toward macrophages, indicating that this essential heterotrimer, which possesses homologs in a wide variety of pathogens, is a unique attractive target for the development of novel antibacterials.


Subject(s)
Carrier Proteins/chemistry , Molecular Chaperones/chemistry , Amino Acid Sequence , Drug Design , Intercellular Signaling Peptides and Proteins , Molecular Sequence Data , Protein Folding , Protein Structure, Secondary
3.
J Biol Chem ; 280(43): 36293-300, 2005 Oct 28.
Article in English | MEDLINE | ID: mdl-16115870

ABSTRACT

Type III secretion (T3S) systems play key roles in pathogenicity of many Gram-negative bacteria and are employed to inject toxins directly into the cytoplasm of target cells. They are composed of over 20 different proteins that associate into a basal structure that traverses both inner and outer bacterial membranes and a hollow, needle-like structure through which toxins travel. The PscF protein is the main component of the Pseudomonas aeruginosa T3S needle. Here we demonstrate that PscF, when purified on its own, is able to form needle-like fibers of 8 nm in width and >1 microm in length. In addition, we demonstrate for the first time that the T3S needle subunit requires two cytoplasmic partners, PscE and PscG, in P. aeruginosa, which trap PscF in a ternary, 1:1:1 complex, thus blocking it in a monomeric state. Knock-out mutants deficient in PscE and PscG are non-cytotoxic, lack PscF, and are unable to export PscF encoded extrachromosomally. Temperature-scanning circular dichroism measurements show that the PscE-PscF-PscG complex is thermally stable and displays a cooperative unfolding/refolding pattern. Thus, PscE and PscG prevent PscF from polymerizing prematurely in the P. aeruginosa cytoplasm and keep it in a secretion prone conformation, strategies which may be shared by other pathogens that employ the T3S system for infection.


Subject(s)
Bacterial Physiological Phenomena , Carrier Proteins/physiology , Molecular Chaperones/physiology , Pseudomonas aeruginosa/metabolism , Amino Acid Sequence , Antigens, Bacterial/chemistry , Bacterial Outer Membrane Proteins/chemistry , Bacterial Proteins/chemistry , Blotting, Western , Carrier Proteins/genetics , Circular Dichroism , Cytoplasm/metabolism , Genetic Vectors , Immunoblotting , Intercellular Signaling Peptides and Proteins , Mass Spectrometry , Membrane Transport Proteins/chemistry , Microscopy, Electron , Molecular Chaperones/genetics , Molecular Sequence Data , Mutation , Polymers/chemistry , Protein Conformation , Temperature , Time Factors , Transgenes
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