biblio

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2013
M. Chandrakesan, Sarkar, B., Mithu, V. Singh, Abhyankar, R. M., Bhowmik, D., Nag, S., Sahoo, B., Shah, R., Gurav, S., Banerjee, R., Dandekar, S., Jose, J. C., Sengupta, N., Madhu, P. K., and Maiti, S., Basic structural motif and major biophysical properties of Amyloid-beta are encoded in the fragment 18-35, Chemical Physics, vol. 422, pp. 80-87, 2013.
N. Sengupta, Competition between adsorption and intrinsic collapse of full-length a beta 1-42 on the surface of a single-walled carbon nanotube: insights from molecular dynamics simulations, Biophysical Journal, vol. 104, no. 2, p. 508A, 2013.
A. K. Jana, Jose, J. C., and Sengupta, N., Critical roles of key domains in complete adsorption of a beta peptide on single-walled carbon nanotubes: insights with point mutations and MD simulations, Physical Chemistry Chemical Physics, vol. 15, no. 3, pp. 837-844, 2013.
J. C. Jose and Sengupta, N., Molecular dynamics simulation studies of the structural response of an isolated A beta(1-42) monomer localized in the vicinity of the hydrophilic TiO2 surface, European Biophysics Journal, vol. 42, no. 6, pp. 487-494, 2013.
A. K. Jana and Sengupta, N., Surface induced collapse of A beta(1-42) with the F19A replacement following adsorption on a single walled carbon nanotube, Biophysical Chemistry, vol. 184, pp. 108-115, 2013.
2014
A. K. Jana and Sengupta, N., Atomistic simulations lend mechanistic insights into plausible ways of perturbing the nucleation thermodynamics of the full-length a beta peptide, Biophysical Journal, vol. 106, no. 2, p. 683A, 2014.
J. C. Jose, Chatterjee, P., and Sengupta, N., Cross dimerization of amyloid-beta and alpha synuclein proteins in aqueous environment: a molecular dynamics simulations study, Plos One, vol. 9, no. 9, p. Article No. : e106883, 2014.
J. C. Jose, Khatua, P., Bansal, N., Sengupta, N., and Bandyopadhyay, S., Microscopic hydration properties of the a beta(1-42) peptide monomer and the globular protein ubiquitin: a comparative molecular dynamics study, Journal of Physical Chemistry B, vol. 118, no. 40, pp. 11591-11604, 2014.
S. B. Bansode, Jana, A. K., Batkulwar, K. B., Warkad, S. D., Joshi, R. S., Sengupta, N., and Kulkarni, M. J., Molecular investigations of protriptyline as a multi-target directed ligand in alzheimer's disease, Plos One, vol. 9, no. 8, p. e105196, 2014.
P. Chatterjee, Bagchi, S., and Sengupta, N., Non-uniform early structural response of globular proteins to cold denaturing conditions: a case study with Yfh1, Journal of Chemical Physics, vol. 141, no. 20, p. 205103, 2014.
2016
D. Chakraborty, Sengupta, N., and Wales, D. J., Conformational energy landscape of the ritonavir molecule, Journal of Physical Chemistry B, vol. 120, no. 19, pp. 4331-4340, 2016.
P. Khatua, Jose, J. C., Sengupta, N., and Bandyopadhyay, S., Conformational features of the Aβ42 peptide monomer and its interaction with the surrounding solvent, Physical Chemistry Chemical Physics, vol. 18, pp. 30144-30159, 2016.
A. K. Jana, Batkulwar, K. B., Kulkarni, M. J., and Sengupta, N., Glycation induces conformational changes in Amyloid-? peptide and enhances its aggregation propensity: molecular insights, Physical Chemistry Chemical Physics, vol. 18, pp. 31446-31458, 2016.
K. B. Batkulwar, Jana, A. K., Godbole, R. K., Khandelwal, P., Sengupta, N., and Kulkarni, M. J., Hydralazine inhibits amyloid beta (Aβ) aggregation and glycation and ameliorates Aβ1–42 induced neurotoxicity, RSC Advances, vol. 6, pp. 108768-108776, 2016.
P. Chatterjee and Sengupta, N., Signatures of protein thermal denaturation and local hydrophobicity in domain specific hydration behavior: a comparative molecular dynamics study, Molecular Biosystems, vol. 12, no. 4, pp. 1139-1150, 2016.
A. K. Jana, Tiwari, M. K., Vanka, K., and Sengupta, N., Unraveling origins of the heterogeneous curvature dependence of polypeptide interactions with carbon nanostructures, Physical Chemistry Chemical Physics, vol. 18, no. 8, pp. 5910-5924, 2016.