Prof G. R. Desiraju's Lab

From OpenWetWare

Revision as of 07:24, 10 July 2006 by Tejenderthakur (Talk | contribs)
Jump to: navigation, search

Drug Design and Discovery

Computational Approaches from X-ray Crystallography

     Intermolecular interactions, especially hydrogen bonds, manifest themselves in somewhat similar ways both in crystals of small organic molecules and large biological macromolecules. We are trying to analyse crystal structures of biological macromolecules with respect to intermolecular interactions and to establish some general principles for their assembly using ideas and concepts of crystal engineering. The possible application of such a study is in the field of drug design. Where drug design is concerned, an overall knowledge is vital to obtain safer drugs. Especially, with the current importance of virtual screening, there is an urgent need to develop methods to efficiently study the chemical space of drug molecules. Our research aims at understanding the overall chemical nature of drug molecules through the study of databases of small molecules (drugs and non-drugs). In this respect there is a continuing effort in our group to develop methods for analysing drug-like and non-drug molecules.

Traditionally drug design has relied more on serendipity than on rational design, especially in the early stages of lead molecule identification. But recent developments in the field of genomics and proteomics have forced the researcher to adopt more rational approaches to drug design to convert the huge amount of raw data into medicinally important information. We follow a dual strategy using both analog and structure based drug design based on the type of information available. In the analog based approach we use 3D-QSAR, pharmacophore generation and de novo design methods. On the other hand the structure based methods include molecular docking and molecular dynamics simulations to understand the basic nature of drug-receptor interactions. When the target structure is not known we try to model it through a computational approach (see illustration) Rational drug design with a flavour of strong and weak intermolecular interactions is being applied to design novel inhibitors targeting diseases like tuberculosis and cancer.   

<img src="Drugdiscovery.png"</img>



and weak hydrogen bonds in the crystal structure of the anti-cancer

drug erlotinib in the kinase domain of EGFR

last updated 10th july 2006 by Tejender thakur email: web address:

Personal tools