1 / 15

Exploring Molecular Dynamics through Time: A Strategy for Understanding Biological Processes

Delve into the realm of molecular kinetics and mechanisms by tracking molecules/cells over time to study synthesis, degradation, and precursor relationships in various experimental conditions. Learn about classic pulse-chase experiments and equilibrium density gradient sedimentation techniques, shedding light on DNA replication processes in E. coli.

tevy
Download Presentation

Exploring Molecular Dynamics through Time: A Strategy for Understanding Biological Processes

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Following Molecules/Cells through TIME to Understand Processing and Processes

  2. An experimental strategy for investigating • kinetics of synthesis or degradation of a molecule • precursor/product relationships • molecular mechanisms (e.g. DNA replication, signal transduction) • which cells give rise to particular structures during development?

  3. Experimental Conditions I • a means of differentially marking a population of molecules or cells • a method for following them through time. Must distinguish labeled from unlabeled at various time points.

  4. Marking a Population of • Molecules • radioactivity (e.g. 35S, 32P) • density • fluorescence • Cells • enzyme expression • morphology (e.g. chick versus quail) • fluorescence

  5. Experimental Conditions II • rapid labeling • the label must be transparent to the process • minimal redistribution of the label during the course of the experiment

  6. Pulse/Chase Is a Prototypical Example for Molecules • cells are initially grown in a medium deficient in a metabolite that will be subsequently used as a label, so that stores are depleted. • add labeled metabolite for a discrete interval and then add an excess of unlabeled metabolite.

  7. Means of detecting population of marked molecules: • Dana and Nathans used polyacrylamide gel electrophoresis and autoradiography with quantitation of counts in bands. • Schroeter et al. used immunoprecipitation, SDS-PAGE and autoradiography • Meselson and Stahl used equilibrium density gradient centrifugation

  8. Meselson & Stahl:a classic pulse chase experiment Question: What is the mechanism (process) by which E. coli DNA is replicated?

  9. conservative distributive semi-conservative

  10. Equilibrium Density Gradient Sedimentation • Pioneered by Meselson, Stahl and Vinograd • Gradient of concentration of salt (CsCl in this case) set up by gravitational force field leading to a density gradient. This occurs relatively rapidly. • DNA travels under the influence of gravitational force until it reaches a point where the density is equal to its own- can't go further into more dense material. • Countervailing process is diffusion of DNA down its concentration gradient. The band width is inversely proportional to molecular weight of the substance because of diffusion.

  11. How would you answer this question today? Look directly at the DNA molecule? Resolution is an issue. Maybe atomic force microscopy What about BrdU labeling? Resolution wouldn’t be good enough to distinguish strands.

More Related