Page 42 - Annual report 2021-22
P. 42

Annual Report 2021-22 |






               Swarnendu Bag

                                                                                                                  25


               Swarnendu  Bag’s  lab  focuses  on  the  study  of  Proteomics  and  Metabolomics  for  early  detection,
               prognosis  and  predictive  marker  discovery  of  different  types  of  cancer  and  metabolic  disorders.
               Presently,  his  lab  is  working  on  cancer  proteomics  and  metabolomics  with  special  reference  to
               immunotherapy in the light of spatiotemporal dimension at single-cell resolution. Tumor cells follow
               different strategies to suppress the immune cells’ metabolism leading to inhibit the functionality of
               immune cells. But the metabolic cross-talk between tumor cells & immune cells was not fully explored.
               Henceforth, to decode these ambiguities regarding the metabolic competition amongst tumor cells
               and  various  types  of  immune  cells  in  the  heterogeneous  niche  of  tumor  microenvironment,  a
               standardized immune-metabolomic & proteomic study‐protocol is very necessary.

                In this work, he will be developing methods for isolating, analyzing and quantifying metabolites and
               proteins from sorted single-type immune cells. This will involve LC-MS/MS method development. In
               the  preliminary  standardization  phase,  isolation  of  total  PBMC  from  normal  human  blood  was
               performed by using lymphoprep reagent (density gradient medium). After counting the total PBMC,
               shorting of CD4+ & CD8+ cells were done by using the FACS system. An LC-MS/MS method to identify
               most  of  the  amino  acids  (Glycine,  Alanine,  Serine,  Proline,  Valine,  Threonine,  Cysteine,  Leucine,
               Asparagine, Glutamine, Lysine, Glutamate, Methionine, Histidine, Phenylalanine, Arginine, Tyrosine &
               Tryptophan) and lactate has been standardized which works optimally for even 0.2 million CD8+ cells
               and  around  1  million  CD4+  cells.  The  lab  is  now  working  towards  method  development  for  the
               detection of TCA intermediate metabolites, lipids, and proteins from less than 0.5 million single-type
               immune cells.













               “A  discovery  must  be  by  definition,  at  variance  with  existing

               knowledge.” — Albert Szent-Gyorgyi
   37   38   39   40   41   42   43   44   45   46   47