Blob-Based Approach to Estimate the Folding Time of Proteins Supported by Pyrene Excimer Fluorescence Experiments

2020 ◽  
Vol 53 (22) ◽  
pp. 9823-9835
Author(s):  
Remi Casier ◽  
Jean Duhamel
Keyword(s):  
RSC Advances ◽  
2021 ◽  
Vol 11 (42) ◽  
pp. 25850-25857
Author(s):  
Igor S. Kovalev ◽  
Leila K. Sadieva ◽  
Olga S. Taniya ◽  
Victoria M. Yurk ◽  
Artem S. Minin ◽  
...  

Simplified computer vision-assisted algorithm for the excimer fluorescence "turn-off" detection of nitro-analytes in aqueous media is described.


2010 ◽  
Vol 88 (3) ◽  
pp. 217-227 ◽  
Author(s):  
Mark Ingratta ◽  
Manoj Mathew ◽  
Jean Duhamel

A series of polystyrenes randomly labeled with 1-pyrenebutanol were prepared by copolymerizing styrene and 1-pyrenebutylacrylate yielding the CoBuE–PS series. Solutions of CoBuE–PS were prepared in nine organic solvents having viscosities ranging from 0.36 to 5.5 mPa·s and the fluorescence spectra and pyrene monomer and excimer fluorescence decays were acquired. Analysis of the fluorescence spectra yielded the IE/IM ratio, whereas analysis of the fluorescence decays with the fluorescence blob model (FBM) yielded the parameters N blobo , <kblob × Nblob> , and k blobo . These parameters were compared to those obtained with two other series of pyrene-labeled polystyrenes, which had been studied earlier, namely CoA–PS and CoE–PS where pyrene was attached to the polymer backbone via a methylamide and benzyl methylether linker, respectively. Although the parameters IE/IM, N blobo , <kblob × Nblob>, and k blobo took different values according to the specific nature of the linker connecting pyrene to the polystyrene backbone, they exhibited trends that were quite similar for all the pyrene-labeled polystyrene constructs. The excellent agreement between the parameters retrieved for the three different types of pyrene-labeled polystyrenes suggests that the FBM accounts satisfyingly for differences in the nature of the label used, while still retrieving information pertinent to the polymer of interest.


1975 ◽  
Vol 97 (11) ◽  
pp. 2977-2978 ◽  
Author(s):  
Brian Brocklehurst ◽  
David C. Bull ◽  
Margaret Evans ◽  
Peter M. Scott ◽  
Gillian Stanney

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1690
Author(s):  
Weize Yuan ◽  
Remi Casier ◽  
Jean Duhamel

The denaturation undergone by α–helical poly(L-glutamic acid) (PLGA) in N,N-dimethylformamide upon addition of guanidine hydrochloride (GdHCl) was characterized by comparing the fluorescence of a series of PLGA constructs randomly labeled with the dye pyrene (Py-PLGA) to that of a series of Py-PDLGA samples prepared from a racemic mixture of D,L-glutamic acid. The process of pyrene excimer formation (PEF) was taken advantage of to probe changes in the conformation of α–helical Py-PLGA. Fluorescence Blob Model (FBM) analysis of the fluorescence decays of the Py-PLGA and Py-PDLGA constructs yielded the average number (<Nblob>) of glutamic acids located inside a blob, which represented the volume probed by an excited pyrenyl label. <Nblob> remained constant for randomly coiled Py-PDLGA but decreased from ~20 to ~10 glutamic acids for the Py-PLGA samples as GdHCl was added to the solution. The decrease in <Nblob> reflected the decrease in the local density of PLGA as the α–helix unraveled in solution. The changes in <Nblob> with GdHCl concentration was used to determine the change in Gibbs energy required to denature the PLGA α–helix in DMF. The relationship between <Nblob> and the local density of macromolecules can now be applied to characterize the conformation of macromolecules in solution.


Polymer ◽  
1988 ◽  
Vol 29 (3) ◽  
pp. 467-470 ◽  
Author(s):  
A. Stroeks ◽  
M. Shmorhun ◽  
A.M. Jamieson ◽  
R. Simha

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