Calculations of protein circular dichroism from first principles Export

@article{citeulike:3925677, abstract = {Understanding the relationship between the amino acid sequence of a protein and its unique, compact 3D structure is one of the grand challenges in molecular biophysics. One particularly exciting approach is time-resolved electronic circular dichroism (CD) spectroscopy, which offers resolution on a nanosecond (or faster) time scale, although it does not provide the spatial resolution of techniques like X-ray crystallography or NMR. The thrust of our work is to underpin fast time scale spectroscopic studies of protein folding with a stronger theoretical foundation. Ultimately, we seek to use molecular dynamics simulations to study the influence of conformational dynamics and conformational transitions on the electronic CD spectra of proteins. We discuss how improved quantum chemical models of individual chromophores, including aromatic sidechains, can be incorporated into calculations of the electronic structure of proteins and their CD. Chirality 16:234-243, 2004. {\copyright} 2004 Wiley-Liss, Inc.}, address = {School of Chemistry, University of Nottingham, University Park, Nottingham, United Kingdom}, author = {Rogers, David M. and Hirst, Jonathan D.}, citeulike-article-id = {3925677}, citeulike-linkout-0 = {http://dx.doi.org/10.1002/chir.20018}, citeulike-linkout-1 = {http://www3.interscience.wiley.com/cgi-bin/abstract/107637532/ABSTRACT}, doi = {10.1002/chir.20018}, journal = {Chirality}, keywords = {ab-initio, cd, protein, spectra}, number = {4}, pages = {234--243}, posted-at = {2009-01-22 19:13:34}, priority = {2}, title = {Calculations of protein circular dichroism from first principles}, url = {http://dx.doi.org/10.1002/chir.20018}, volume = {16}, year = {2004} }

TY - JOUR ID - citeulike:3925677 L3 - citeulike-article-id:3925677 N2 - Understanding the relationship between the amino acid sequence of a protein and its unique, compact 3D structure is one of the grand challenges in molecular biophysics. One particularly exciting approach is time-resolved electronic circular dichroism (CD) spectroscopy, which offers resolution on a nanosecond (or faster) time scale, although it does not provide the spatial resolution of techniques like X-ray crystallography or NMR. The thrust of our work is to underpin fast time scale spectroscopic studies of protein folding with a stronger theoretical foundation. Ultimately, we seek to use molecular dynamics simulations to study the influence of conformational dynamics and conformational transitions on the electronic CD spectra of proteins. We discuss how improved quantum chemical models of individual chromophores, including aromatic sidechains, can be incorporated into calculations of the electronic structure of proteins and their CD. Chirality 16:234-243, 2004. © 2004 Wiley-Liss, Inc. IS - 4 JF - Chirality AD - School of Chemistry, University of Nottingham, University Park, Nottingham, United Kingdom EP - 243 TI - Calculations of protein circular dichroism from first principles VL - 16 SP - 234 KW - ab-initio KW - cd KW - protein KW - spectra AU - Rogers, David AU - Hirst, Jonathan PY - 2004/// UR - http://dx.doi.org/10.1002/chir.20018 ER -