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3: Protein Engineering (Module 2) - Biology

3: Protein Engineering (Module 2) - Biology


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Instructors: Alan Jasanoff and Agi Stachowiak

In this experiment, you will modify a protein called inverse pericam (developed by Nagai, et al.) in order to affect its functions as a sensor. Inverse pericam (IPC) comprises a permuted fluorescent protein linked to a calcium sensor. The "inverse" in the name refers to the fact that this protein shines brightly in the absence of calcium, but dimly once calcium is added. The dissociation constant KD of wild-type IPC with respect to calcium is reported to be 0.2 μM (see also figure below). Your goal will be to shift this titration curve or change its steepness by altering one of the calcium binding sites in IPC's calcium sensor portion. You will modify inverse pericam at the gene level using a process called site-directed mutagenesis, express the resultant protein in a bacterial host, and finally purify your mutant protein and assay its calcium-binding activity via fluorescence. In the course of this module, we will consider the benefits and drawbacks of different approaches to protein design, and the types of scientific investigations and applications enabled by fluorescently tagged biological molecules.

Reference: Nagai, T., et al. "Circularly Permuted Green Fluorescent Proteins Engineered to Sense Ca2+." PNAS 98, no. 6 (March 6, 2001): 3197-3202. [Open Access]

We gratefully acknowledge 20.109 instructor Natalie Kuldell for helpful discussions during the development of this module, as well as for her prior work in developing a related module in the Spring 2007 course.


Watch the video: Genetic circuit walkthrough of Module 2: Encapsulation of the proteins of interest (October 2022).