The topic of how a protein folds has been a major area of research for several decades; however, important details about this process are still undetermined. Experimental limitations in the study of protein folding are a result of no technique possessing both the necessary spatial and temporal resolution. This Thesis presents several studies conducted with the goal of expanding upon the experimentalist\u27s toolbox, involving new methods of interrogating and/or perturbing protein systems of interest. The early chapters of this Thesis describe our efforts using established synthetic methods to extend the utility of infrared spectroscopy in the study of protein folding. Specifically, we show that, using the strategy of cysteine alkylation, we...