Abstract: Methods are disclosed utilizing single-molecule proteomics with dynamic probes to accomplish a variety of protein analytic applications. A panel of probes, when used in combination, can resolve and quantify a proteome in a simple assay detecting transient binding to single protein targets.

Abstract: A method for detecting point mutations in DNA using a fluorescently labeled oligomeric probe and Forster resonance energy transfer (FRET) is disclosed. The selected probe is initially labeled at each end with a fluorescence dye, which act together as a donor/acceptor pair for FRET. The fluorescence emission from the dyes changes dramatically from the duplex stage, wherein the probe is hybridized to the complementary strand of DNA, to the single strand stage, when the probe is melted to become detached from the DNA. The change in fluorescence is caused by the dyes coming into closer proximity after melting occurs and the probe becomes detached from the DNA strand. The change in fluorescence emission as a function of temperature is used to calculate the melting temperature of the complex or Tm. In the case where there is a base mismatch between the probe and the DNA strand, indicating a point mutation, the Tm has been found to be significantly lower than the Tm for a perfectly match probe/stand duplex.

Abstract: A method for detecting point mutations in DNA using a fluorescently labeled oligomeric probe and Forster resonance energy transfer (FRET) is disclosed. The selected probe is initially labeled at each end with a fluorescence dye, which act together as a donor/acceptor pair for FRET. The fluorescence emission from the dyes changes dramatically from the duplex stage, wherein the probe is hybridized to the complementary strand of DNA, to the single strand stage, when the probe is melted to become detached from the DNA. The change in fluorescence is caused by the dyes coming into closer proximity after melting occurs and the probe becomes detached from the DNA strand. The change in fluorescence emission as a function of temperature is used to calculate the melting temperature of the complex or Tm. In the case where there is a base mismatch between the probe and the DNA strand, indicating a point mutation, the Tm has been found to be significantly lower than the Tm for a perfectly match probe/stand duplex.

Abstract: A method for detecting point mutations in DNA using a fluorescently labeled oligomeric probe and Forster resonance energy transfer (FRET) is disclosed. The selected probe is initially labeled at each end with a fluorescence dye, which act together as a donor/acceptor pair for FRET. The fluorescence emission from the dyes changes dramatically from the duplex stage, wherein the probe is hybridized to the complementary strand of DNA, to the single strand stage, when the probe is melted to become detached from the DNA. The change in fluorescence is caused by the dyes coming into closer proximity after melting occurs and the probe becomes detached from the DNA strand. The change in fluorescence emission as a function of temperature is used to calculate the melting temperature of the complex or Tm. In the case where there is a base mismatch between the probe and the DNA strand, indicating a point mutation, the Tm has been found to be significantly lower than the Tm for a perfectly match probelstand duplex.