Molecular Biology Commons^™

Nf-Kappab Signaling Pathways In Mammalian And Insect Innate Immunity, Neal S. Silverman, Tom Maniatis

Neal Silverman

In this review, we discuss recent advances in understanding the signaling pathways in mammalian and Drosophila innate immunity, with emphasis on the mechanisms by which NF-kappaB/Rel family proteins are activated.

Role Of A Conserved Glutamate Residue In The Escherichia Coli Seca Atpase Mechanism, Don Oliver

Don Oliver

Escherichia coli SecA uses ATP to drive the transport of proteins across cell membranes. Glutamate 210 in the "DEVD" Walker B motif of the SecA ATP-binding site has been proposed as the catalytic base for ATP hydrolysis (Hunt, J. F., Weinkauf, S., Henry, L., Fak, J. J., McNicholas, P., Oliver, D. B., and Deisenhofer, J. (2002) Science 297, 2018-2026). Consistent with this hypothesis, we find that mutation of glutamate 210 to aspartate results in a 90-fold reduction of the ATP hydrolysis rate compared with wild type SecA, 0.3 s(-1) versus 27 s(-1), respectively. SecA-E210D also releases ADP at a slower …

Dimeric Seca Is Essential For Protein Translocation, Don Oliver

Don Oliver

SecA facilitates bacterial protein translocation by its association with presecretory or membrane proteins and the SecYEG translocon channel. Once assembled, SecA ATPase undergoes cycles of membrane insertion and retraction at SecYEG that drive protein translocation in a stepwise fashion. SecA exists in equilibrium between a monomer and dimer, and association with its translocation ligands shifts this equilibrium dramatically. Here, we examined the proposal that protein translocation can occur by means of a SecA monomer. We produced a mutant SecA protein lacking residues 2-11, which was found to exist mostly as a monomer, and it was unable to complement a conditional-lethal …

Reexamination Of The Role Of The Amino Terminus Of Seca In Promoting Its Dimerization And Functional State, Don Oliver

Don Oliver

No abstract provided.

Seca Dimer Cross-Linked At Its Subunit Interface Is Functional For Protein Translocation, Don Oliver

Don Oliver

SecA facilitates protein transport across the eubacterial plasma membrane by its association with cargo proteins and the SecYEG translocon, followed by ATP-driven conformational changes that promote protein translocation in a stepwise manner. Whether SecA functions as a monomer or a dimer during this process has been the subject of considerable controversy. Here we utilize cysteine-directed mutagenesis along with the crystal structure of the SecA dimer to create a cross-linked dimer at its subunit interface, which was normally active for in vitro protein translocation.

In Vivo Membrane Topology Of Escherichia Coli Seca Atpase Reveals Extensive Periplasmic Exposure Of Multiple Functionally Important Domains Clustering On One Face Of Seca, Don Oliver

Don Oliver

No abstract provided.

A Feedback Circuit Involving Let-7-Family Mirnas And Daf-12 Integrates Environmental Signals And Developmental Timing In Caenorhabditis Elegans, Christopher M. Hammell, Xantha Karp, Victor R. Ambros

Victor R. Ambros

Animal development is remarkably robust; cell fates are specified with spatial and temporal precision despite physiological and environmental contingencies. Favorable conditions cause Caenorhabditis elegans to develop rapidly through four larval stages (L1-L4) to the reproductive adult. In unfavorable conditions, L2 larvae can enter the developmentally quiescent, stress-resistant dauer larva stage, enabling them to survive for prolonged periods before completing development. A specific progression of cell division and differentiation events occurs with fidelity during the larval stages, regardless of whether an animal undergoes continuous or dauer-interrupted development. The temporal patterning of developmental events is controlled by the heterochronic genes, whose products …

Uv Resonance Raman And Circular Dichroism Studies Of A Dna Duplex Containing An A3t3 Tract: Evidence For A Premelting Transition And Three-Centered H-Bonds, Ishita Mukerji

Ishita Mukerji

The presence of A(n) and A(n)T(n) tracts in double-helical sequences perturbs the structural properties of DNA molecules, resulting in the formation of an alternate conformation to standard B-DNA known as B'-DNA. Evidence for a transition occurring prior to duplex melting in molecules containing A(n) tracts was previously detected by circular dichroism (CD) and calorimetric studies. This premelting transition was attributed to a conformational change from B'- to B-DNA. Structural features of A(n) and A(n)T(n) tracts revealed by X-ray crystallography include a large degree of propeller twisting of adenine bases, narrowed minor grooves, and the formation of three-centered H-bonds between dA …

Spectroscopic And Molecular Dynamics Evidence For A Sequential Mechanisms For The A-To-B Transition In Dna, Ishita Mukerji

Ishita Mukerji

The A-to-B form transition has been examined in three DNA duplexes, d(CGCGAATTCGCG)2, d(CGCGAATTGCGC), and d(CGCAAATTTCGC), using circular dichroism spectroscopy, ultraviolet resonance Raman (UVRR) spectroscopy, and molecular dynamics (MD) simulation. Circular dichroism spectra confirm that these molecules adopt the A form under conditions of reduced water activity. UVRR results, obtained under similar conditions, suggest that the transition involves a series of intermediate forms between A and B. Cooperative and distinct transitions were observed for the bases and the sugars. Independent MD simulations on d(CGCGAATTCGCG)2 show a spontaneous change from the A to B form in aqueous solution and describe a kinetic …

Integration Host Factor (Ihf) Dictates The Structure Of Polyamine-Dna Condensates: Implications For The Role Of Ihf In The Compaction Of Bacterial Chromatin, Ishita Mukerji

Ishita Mukerji

No abstract provided.

Effects Of Hu Binding On The Equilibrium Cyclization Of Mismatched, Curved And Normal Dna, Ishita Mukerji

Ishita Mukerji

No abstract provided.

Conserved Residues In The Delta Subunit Help The E. Coli Clamp Loader, Gamma Complex, Target Primer-Template Dna For Clamp Assembly, Manju Hingorani

Manju Hingorani

The Escherichia coli clamp loader, gamma complex (gamma(3)deltadelta'lambdapsi), catalyzes ATP-driven assembly of beta clamps onto primer-template DNA (p/tDNA), enabling processive replication. The mechanism by which gamma complex targets p/tDNA for clamp assembly is not resolved. According to previous studies, charged/polar amino acids inside the clamp loader chamber interact with the double-stranded (ds) portion of p/tDNA. We find that dsDNA, not ssDNA, can trigger a burst of ATP hydrolysis by gamma complex and clamp assembly, but only at far higher concentrations than p/tDNA. Thus, contact between gamma complex and dsDNA is necessary and sufficient, but not optimal, for the reaction, and …

Protein Purification For Structural Genomics, Rachele M. Hendricks-Sturrup

Rachele M Hendricks-Sturrup