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Dissecting coherent vibrational spectra of small proteins into secondary structural elements by sensitivity analysis.


ABSTRACT: The response of proteins to sequences of femtosecond infrared pulses provides a multidimensional view into their equilibrium distribution of structures and snapshot pictures of fast-triggered dynamical events. Analyzing these experiments requires advanced computational tools for assigning regions in the resulting multi-dimensional correlation plots to specific secondary-structure elements and their couplings. A differential sensitivity analysis technique based on a perturbation of the local (real space) Hamiltonian is developed to achieve that goal. Application to the amide I region of a small globular protein reveals regions associated with the alpha-helix, beta-sheet, and their coupling. Comparison of signals generated in different directions shows that the double-quantum-coherence signal has a higher sensitivity to the couplings compared with the single-quantum-coherence (photon echo) technique.

SUBMITTER: Zhuang W 

PROVIDER: S-EPMC1140409 | biostudies-literature | 2005 May

REPOSITORIES: biostudies-literature

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Dissecting coherent vibrational spectra of small proteins into secondary structural elements by sensitivity analysis.

Zhuang Wei W   Abramavicius Darius D   Mukamel Shaul S  

Proceedings of the National Academy of Sciences of the United States of America 20050513 21


The response of proteins to sequences of femtosecond infrared pulses provides a multidimensional view into their equilibrium distribution of structures and snapshot pictures of fast-triggered dynamical events. Analyzing these experiments requires advanced computational tools for assigning regions in the resulting multi-dimensional correlation plots to specific secondary-structure elements and their couplings. A differential sensitivity analysis technique based on a perturbation of the local (rea  ...[more]

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