SEARCH · Search NASA
Results for “FRETTING”
Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Fast, Ratiometric FRET from Quantum Dot Conjugated Stabilized Single Chain Variable Fragments for Quantitative Botulinum Neurotoxin Sensing
Explore the source record for details and available documents.
Quantum Dot–DNA FRET Conjugates for Direct Analysis of Methylphosphonic Acid in Complex Media
Not Available
Conformational Ensembles of an Intrinsically Disordered Protein Consistent with NMR, SAXS, and Single-Molecule FRET
Abstract not provided
Determination of cellulase colocalization on cellulose fiber with quantitative FRET measured by acceptor photobleaching and spectrally unmixing fluorescence microscopy
Explore the source record for details and available documents.
Sequential data assimilation for single-molecule FRET photon-counting data
Data assimilation is a statistical method designed to improve the quality of numerical simulations in combination with real observations. Here, we develop a sequential data assimilation method that incorporates one-dimensional time-series data of smFRET (single-molecule Förster resonance energy transfer) photon-counting into conformational ensembles of biomolecules derived from “replicated” molecular dynamics (MD) simulations. A particle filter using a large number of “replicated” MD simulations with a likelihood function for smFRET photon-counting data is employed to screen the conformational ensembles that match the experimental data. We examine the performance of the method using emulated smFRET data and coarse-grained (CG) MD simulations of a dye-labeled polyproline-20. The method estimates the dynamics of the end-to-end distance from smFRET data as well as revealing that of latent conformational variables. The particle filter is also able to correct model parameter dependence in CG MD simulations. We discuss the applicability of the method to real experimental data for conformational dynamics of biomolecules.
Förster resonance energy transfer: Role of diffusion of fluorophore orientation and separation in observed shifts of FRET efficiency
Not Available
FRET Based Biosensors for CBRN Threat Detection
Biosensors are devices used to detect the presence/concentration of a biological analyte. Biosensors consist of three parts: 1) a component that recognizes the analyte and produces a signal, 2) a signal transducer, and 3) a reader device. A multiplexed biosensor combines different biosensors for increased detection capabilities.
FRET-based reporters for the direct visualization of abscisic acid concentration changes and distribution in Arabidopsis
Not Available
Single-molecule FRET unveils induced-fit mechanism for substrate selectivity in flap endonuclease 1
Human flap endonuclease 1 (FEN1) and related structure-specific 5’nucleases precisely identify and incise aberrant DNA structures during replication, repair and recombination to avoid genomic instability. Yet, it is unclear how the 5’nuclease mechanisms of DNA distortion and protein ordering robustly mediate efficient and accurate substrate recognition and catalytic selectivity. Here, single-molecule sub-millisecond and millisecond analyses of FEN1 reveal a protein-DNA induced-fit mechanism that efficiently verifies substrate and suppresses off-target cleavage. FEN1 sculpts DNA with diffusion-limited kinetics to test DNA substrate. This DNA distortion mutually ‘locks’ protein and DNA conformation and enables substrate verification with extreme precision. Strikingly, FEN1 never misses cleavage of its cognate substrate while blocking probable formation of catalytically competent interactions with noncognate substrates and fostering their pre-incision dissociation. These findings establish FEN1 has practically perfect precision and that separate control of induced-fit substrate recognition sets up the catalytic selectivity of the nuclease active site for genome stability.
Characterizing 3D RNA structure by single molecule FRET
Explore the source record for details and available documents.
Investigation of Fretting Corrosion by Microscopic Observation
Explore the source record for details and available documents.
Coefficient of Friction and Damage to Contact Area During the Early Stages of Fretting I : Glass, Copper, or Steel Against Copper
Explore the source record for details and available documents.
Coefficient of Friction and Damage to Contact Area During the Early Stages of Fretting II : Steel, Iron, Iron Oxide, and Glass Combinations
Explore the source record for details and available documents.
A Fundamental Investigation of Fretting Corrosion
Explore the source record for details and available documents.
Formalizing and Analyzing Requirements with FRET
Formal verification and simulation are powerful tools to validate requirements against complex systems. Requirements are developed in early stages of the software lifecycle and are typically written in ambiguous natural language. There is a gap between such requirements and formal notations that can be used by verification tools, and lack of support for proper association of requirements with software artifacts for verification. We propose to write requirements in an intuitive, structured natural language with formal semantics, and to support formalization and model/code verification as a smooth, well-integrated process. To this end, we have developed an end-to-end, open source requirements analysis framework that checks Simulink models against requirements written structured natural language.
Capturing & Analyzing Requirements with FRET
Explore the source record for details and available documents.