Keyword search (4,163 papers available)

"Jankowiak R" Authored Publications:

Title Authors PubMed ID
1 High-Resolution Frequency-Domain Spectroscopic and Modeling Studies of Photosystem I (PSI), PSI Mutants and PSI Supercomplexes Zazubovich V; Jankowiak R; 38612659
PHYSICS
2 Frequency-Domain Spectroscopic Study of the Photosystem I Supercomplexes, Isolated IsiA Monomers, and the Intact IsiA Ring Reinot T; Khmelnitskiy A; Zazubovich V; Toporik H; Mazor Y; Jankowiak R; 36065077
PHYSICS
3 How Well Does the Hole-Burning Action Spectrum Represent the Site-Distribution Function of the Lowest-Energy State in Photosynthetic Pigment-Protein Complexes? Zazubovich V, Jankowiak R 31265294
CHEMISTRY
4 Low-temperature protein dynamics of the B800 molecules in the LH2 light-harvesting complex: spectral hole burning study and comparison with single photosynthetic complex spectroscopy. Grozdanov D, Herascu N, Reinot T, Jankowiak R, Zazubovich V 20166717
PHYSICS
5 Effects of the distributions of energy or charge transfer rates on spectral hole burning in pigment-protein complexes at low temperatures. Herascu N, Ahmouda S, Picorel R, Seibert M, Jankowiak R, Zazubovich V 22046956
PHYSICS
6 Spectral hole burning, recovery, and thermocycling in chlorophyll-protein complexes: distributions of barriers on the protein energy landscape. Najafi M, Herascu N, Seibert M, Picorel R, Jankowiak R, Zazubovich V 22957798
PHYSICS
7 Modeling of various optical spectra in the presence of slow excitation energy transfer in dimers and trimers with weak interpigment coupling: FMO as an example. Herascu N, Kell A, Acharya K, Jankowiak R, Blankenship RE, Zazubovich V 24506338
PHYSICS
8 On the Controversial Nature of the 825 nm Exciton Band in the FMO Protein Complex. Kell A, Acharya K, Zazubovich V, Jankowiak R 26269993
PHYSICS
9 On the Conflicting Estimations of Pigment Site Energies in Photosynthetic Complexes: A Case Study of the CP47 Complex. Reinot T, Chen J, Kell A, Jassas M, Robben KC, Zazubovich V, Jankowiak R 27279733
PHYSICS

 

Title:On the Conflicting Estimations of Pigment Site Energies in Photosynthetic Complexes: A Case Study of the CP47 Complex.
Authors:Reinot TChen JKell AJassas MRobben KCZazubovich VJankowiak R
Link:https://www.ncbi.nlm.nih.gov/pubmed/27279733?dopt=Abstract
Publication:
Keywords:
PMID:27279733 Category:Anal Chem Insights Date Added:2019-06-04
Dept Affiliation: PHYSICS
1 Department of Chemistry, Kansas State University, Manhattan, KS, USA.
2 Department of Physics, Concordia University, Montreal, QC, Canada.
3 Department of Chemistry, Kansas State University, Manhattan, KS, USA.; Department of Physics, Kansas State University, Manhattan, KS, USA.

Description:

On the Conflicting Estimations of Pigment Site Energies in Photosynthetic Complexes: A Case Study of the CP47 Complex.

Anal Chem Insights. 2016;11:35-48

Authors: Reinot T, Chen J, Kell A, Jassas M, Robben KC, Zazubovich V, Jankowiak R

Abstract

We focus on problems with elucidation of site energies [Formula: see text] for photosynthetic complexes (PSCs) in order to raise some genuine concern regarding the conflicting estimations propagating in the literature. As an example, we provide a stern assessment of the site energies extracted from fits to optical spectra of the widely studied CP47 antenna complex of photosystem II from spinach, though many general comments apply to other PSCs as well. Correct values of [Formula: see text] for chlorophyll (Chl) a in CP47 are essential for understanding its excitonic structure, population dynamics, and excitation energy pathway(s). To demonstrate this, we present a case study where simultaneous fits of multiple spectra (absorption, emission, circular dichroism, and nonresonant hole-burned spectra) show that several sets of parameters can fit the spectra very well. Importantly, we show that variable emission maxima (690-695 nm) and sample-dependent bleaching in nonresonant hole-burning spectra reported in literature could be explained, assuming that many previously studied CP47 samples were a mixture of intact and destabilized proteins. It appears that the destabilized subpopulation of CP47 complexes could feature a weakened hydrogen bond between the 13(1)-keto group of Chl29 and the PsbH protein subunit, though other possibilities cannot be entirely excluded, as discussed in this work. Possible implications of our findings are briefly discussed.

PMID: 27279733 [PubMed]





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