Pore-Forming Toxins

Structure-Function Studies in the Context of Host-Pathogen Interaction and Immunity

Prof. Kausik Chattopadhyay, PhD, FNASc

Department of Biological Sciences

Indian Institute of Science Education and Research Mohali

IISER Mohali, Sector 81, SAS Nagar, Mohali, Punjab 140306, India.

E-mail: kausik[at]iisermohali.ac.in

Editorial Board Member of Journal of Bacteriology (American Society for Microbiology, ASM)

PhD and post-doctoral research opportunity: in the area of biochemistry/cell-biology/immunobiology of pore-forming protein toxins.

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Highlights:

-Dr. Kausik Chattopadhyay is the recipient of the “C. R. Krishna Murti Award” of Society of Biological Chemists (India) for the year 2021 for his contributions in the field of Biochemistry and Allied Sciences.

-Dr. Kausik Chattopadhyay is elected as a Fellow of National Academy of Sciences, India (NASI) in the year 2019. 

-Book volume co-edited by Dr. Kausik Chattopadhyay: Biochemical and Biophysical Roles of Cell Surface Molecules to by published by Springer in the series Advances in Experimental Medicine and Biology.

-"Interdisciplinary research: personal memoir of a biochemist" by Kausik Chattopadhyay.

-11th International Symposium on Cell Surface Macromolecules (11th ISCSM) at IISER Mohali, 24-28 February 2017.

-Dr. Kausik Chattopadhyay has been selected as the recipient of DBT National BioScience Award for Career Development 2014.


Research Interest of Our Lab: Structure-Function Studies on Pore-Forming Protein Toxins.

Pore-forming protein toxins (PFTs) represent a special class of membrane damaging cytolytic proteins, and they are found in wide spectrum of organisms ranging from bacteria to humans. They exert their toxic effects by punching 'holes' into target cell membrane, thus destroying the natural permeability barrier function of the cell membrane. PFTs are, in general, synthesized as water-soluble monomeric molecules, and in contact with target cell membranes they form membrane-inserted oligomeric pores. However, in spite of sharing this overall general scheme, PFTs differ significantly from each other in the intricate details of their pore formation mechanisms. A major mechanistic challenge associated with the membrane pore formation process by PFTs is elucidating the folding pathways that ensure thermodynamic compatibility of the water-soluble monomeric and the membrane-inserted oligomeric form of the toxin with aqueous and lipid milieu, respectively. One of the major research interests of my group is focused on studying structure-function relationship of some of the prominent bacterial PFTs. The critical issues we address are:

1. Mechanistic details of oligomeric membrane channel formation by PFTs.

2. Mechanism(s) associated with cellular responses triggered by PFTs.


Publications from the lab:

FASEB Journal. 36(10):e22557. doi: 10.1096/fj.202200788R. [#Equal contribution][*Joint corresponding authors].