a) Single molecule RNA FISH in Bacillus subtilis
-smFISH was established and tested on several classes of mRNAs. Firstly, several localized proteins (cell division, polar, cytoskeletal proteins) of B. subtilis were fused to GFP and checked for their correct localization within the cell. Multiple fluorescent DNA probes were designed to bind and detect GFP mRNA. Fusion of GFP to the desired targets therefore allowed us visualize individual mRNAs for any GFP tagged gene using the same set of fluorescent probes. However, the mRNA localization of several target proteins did not co-localize with their respective mRNAs. The results of smFISH were disseminated at the general meeting of Bacterial Cell biology labs at the host Institute (SILS, University of Amsterdam) and 1st year bachelor students of microbiology course at University of Amsterdam as a lecture.
b) Mem-seq: A novel technique to identify membrane proximal RNAs
-A new cross-linking based approach was developed to fix the localized mRNA to the bacterial membrane. After several iterations using different fixative agents, I was able to optimize the fixation and extraction of localized mRNAs from purified bacterial membrane. Next generation sequencing analysis of the isolated RNA revealed enrichment of several mRNAs encoding for inner membrane proteins in the membrane fraction compared to the total RNA analysis. The results from this technique were presented at the Amsterdam microbiology lecture series (AMZA 2018) and annual day of the host Institute (SILS day 2018).