This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The diagonalization of the stochastic Liouville (SL) matrix using the Lanczos algorithm (LA) is optimized with the aid of the conjugate (CG) method for calculating 2D-ELDOR spectra in the slow-motional regime. In each step of the LA recursion, the convergence is monitored according to the residual norm calculated in the CG iterations. Thus the methods of the CG and LA can be coupled together to tri-diagonalize a large symmetric and complex sparse matrix efficiently. The LA-CG has been very successfully used to tri-diagonalize the SLE matrix in the slow-motional regime. However, due to the loss of orthogonality in the LA vectors, we found that the LA-CG method can break down in calculating spectra in the very slow-motional regime. This is mainly due to the fact that CG requires the residual norm to calculate the solution direction in each iteration. This indicates that the whole algorithm would be spoiled due to the loss of orthogonality after a certain number of LA projections. This would be particularly true when one calculates a very slow-motional spectrum that requires a large number of LA projections in order to adequately obtain good eigenvalues. The quasi-minimal residual (QMR), which was originally developed to be a linear equation solver, has been adapted for determining the number of LA projections in our program. In the QMR method, the solution vector is obtained by minimizing the quasi-residual norm, using QR factorization. It is of great advantage to us to replace CG with QMR to determine the number of LA projections, because the residual norm is NOT used iteratively as in the CG method to determine the solution direction in each iteration. Therefore, this LA-QMR method that we utilize provides an advantage of avoiding the breakdown noted above.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR016292-10
Application #
8172118
Study Section
Special Emphasis Panel (ZRG1-BCMB-K (40))
Project Start
2010-09-01
Project End
2011-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
10
Fiscal Year
2010
Total Cost
$2,896
Indirect Cost
Name
Cornell University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
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