Aug
12
Mon
2013
Invited Talk: Discovery, engineering and applications of Blue Fish Protein with Red Flourescence @ Sathyam Hall
Aug 12 @ 10:00 am – 10:15 am

RamaswamyS. Ramaswamy, Ph.D.
CEO of c-CAMP, Dean, inStem, NCBS, Bangalore, India


Discovery, engineering and applications of Blue Fish Protein with Red Fluorescence

Swagatha Ghosh, Chi-Li Yu, Daniel Ferraro,  Sai Sudha, Wayne Schaefer, David T Gibson and S. Ramaswamy

Fluorescent proteins and their applications have revolutionized our understanding of biology significantly.  In spite of several years since the discovery of the classic GFP, proteins of this class are used as the standard flag bearers.  We have recently discovered a protein from the fish Sanders vitrius that shows interesting fluorescent properties – including a 280 nm stoke shift and infrared emission.  The crystal structure of the wild type protein shows that it is a tetramer.  We have engineered mutations to make a monomer with very similar fluorescent properties. We have used this protein for tissue imaging as well as for in cell-fluorescence successfully

Ramaswamy (1) Ramaswamy (2) Ramaswamy (3) Ramaswamy (4)

Aug
13
Tue
2013
Delegate Talk: Insilico Analysis of hypothetical proteins from Leishmania donovani: A Case study of a membrane protein of the MFS class reveals their plausible roles in drug resistance @ Sathyam Hall
Aug 13 @ 3:35 pm – 3:50 pm
Delegate Talk: Insilico Analysis of hypothetical proteins from Leishmania donovani: A Case study of a membrane protein of the MFS class reveals their plausible roles in drug resistance @ Sathyam Hall | Vallikavu | Kerala | India

Nitish Sathyanrayanan, Sandesh Ganji and Holenarsipur Gundurao Nagendra.


Insilico Analysis of hypothetical proteins from Leishmania donovani: A Case study of a membrane protein of the MFS class reveals their plausible roles in drug resistance

Kala-azar or visceral leishmaniais (VL), caused by protozoan parasite Leishmania donovani, is one of the leading causes of morbidity and mortality in Bihar, India (Guerin et al. 2002; Mubayi et al. 2010). The disease is transmitted to the humans mainly by the vector, Phlebotmus argentipes, commonly known as Sand fly. The majority of VL (> 90%) occurs in only six countries: Bangladesh, India, Nepal, Sudan, Ethiopia and Brazil (Chappuis et al. 2007). In the Indian subcontinent, about 200 million people are estimated to be at risk of developing VL and this region harbors an estimated 67% of the global VL disease burden. The Bihar state only has captured almost 50% cases out of total cases in Indian sub-continent (Bhunia et al. 2013). ‘Conserved hypothetical’ proteins pose a challenge not just to functional genomics, but also to biology in general (Galperin and Koonin 2004). Leishmania donovani (strain BPK282A1) genome consists of a staggering ∼65% of hypothetical proteins. These uncharacterized proteins may enable better appreciation of signalling pathways, general metabolism, stress response and even drug resistance.

Aug
14
Wed
2013
Delegate Talk: Development of Supercritical Fluid Chromatography methods for the replacement of existing USP Normal phase liquid chromatography methods @ Amriteshwari Hall
Aug 14 @ 12:01 pm – 12:11 pm
Delegate Talk: Development of Supercritical Fluid Chromatography methods for the replacement of existing USP Normal phase liquid chromatography methods @ Amriteshwari Hall | Vallikavu | Kerala | India

Syed Salman Lateef and Vinayak A K


Development of Supercritical Fluid Chromatography methods for the replacement of existing USP Normal phase liquid chromatography methods

Normal phase liquid chromatography methods often have long run times and involve environmentally toxic/costly solvents. Supercritical chromatography methods on the other hand are faster, inexpensive, and eco-friendly. The low viscous supercritical carbon dioxide operates at high flow rates compared to LC without losing separation efficiency. In this work, SFC methods are developed to replace three United States Pharmacopeial (USP) normal phase achiral methods – prednisolone, tolazamide and cholecalciferol. System suitability parameters of the normal phase method are compared against the SFC method. Precision, linearity and robustness of the new SFC methods are demonstrated. SFC methods were found to be cost effective in terms of analysis time and solvent savings. The SFC method does not require purchase and disposal of expensive environmentally hazardous chemicals. Hence, the newly developed SFC method provides a faster and safer solution.