Gas phase folding of an (Ala)4 neutral peptide chain: spectroscopic evidence for the formation of a β-hairpin H-bonding pattern

2009 ◽  
Vol 11 (48) ◽  
pp. 11385 ◽  
Author(s):  
Eric Gloaguen ◽  
Rodolphe Pollet ◽  
François Piuzzi ◽  
Benjamin Tardivel ◽  
Michel Mons
2005 ◽  
Vol 127 (5) ◽  
pp. 1388-1389 ◽  
Author(s):  
Wutharath Chin ◽  
Isabelle Compagnon ◽  
Jean-Pierre Dognon ◽  
Clélia Canuel ◽  
François Piuzzi ◽  
...  

2014 ◽  
Vol 50 (94) ◽  
pp. 14767-14770 ◽  
Author(s):  
C. Fraschetti ◽  
M. Montagna ◽  
L. Guarcini ◽  
L. Guidoni ◽  
A. Filippi

The Na+–G4 adduct exists as a mixture of two metastable populations, rapidly interconverting at room temperature.


2008 ◽  
Vol 465 (4-6) ◽  
pp. 193-196 ◽  
Author(s):  
Gi Woo Lee ◽  
Hyeon Geun Ahn ◽  
Tae Kyu Kim ◽  
Sang Kuk Lee

Author(s):  
Sjors Bakels ◽  
Sebastiaan Porskamp ◽  
Anouk Rijs

The spontaneous aggregation of proteins and peptides is widely studied due to its relation to neurodegenerative diseases. To understand the underlying principles of peptide aggregation, elucidation of structure and structural changes upon their formation is key. This level of detail can be obtained by studying the peptide self-assembly in the gas phase. Structural characterization of aggregates is mainly done on charged species, as adding charges is an intrinsic part of the technique to bring molecules into the gas phase. Studying neutral peptide aggregates will complement the existing picture. These studies are restricted to dimers due to experimental limitations. Here, we present advances in laser desorption molecular beam spectroscopy to form neutral peptide aggregates in the gas phase consisting of up to fourteen monomeric peptides. The combination with IR-UV spectroscopy allowed us to select each aggregate by size and subsequently characterize its structure.


2019 ◽  
Author(s):  
Sjors Bakels ◽  
Sebastiaan Porskamp ◽  
Anouk Rijs

The spontaneous aggregation of proteins and peptides is widely studied due to its relation to neurodegenerative diseases. To understand the underlying principles of peptide aggregation, elucidation of structure and structural changes upon their formation is key. This level of detail can be obtained by studying the peptide self-assembly in the gas phase. Structural characterization of aggregates is mainly done on charged species, as adding charges is an intrinsic part of the technique to bring molecules into the gas phase. Studying neutral peptide aggregates will complement the existing picture. These studies are restricted to dimers due to experimental limitations. Here, we present advances in laser desorption molecular beam spectroscopy to form neutral peptide aggregates in the gas phase consisting of up to fourteen monomeric peptides. The combination with IR-UV spectroscopy allowed us to select each aggregate by size and subsequently characterize its structure.


2016 ◽  
Vol 138 (8) ◽  
pp. 2849-2857 ◽  
Author(s):  
Nicole L. Burke ◽  
Andrew F. DeBlase ◽  
James G. Redwine ◽  
John R. Hopkins ◽  
Scott A. McLuckey ◽  
...  

2010 ◽  
Vol 132 (34) ◽  
pp. 11860-11863 ◽  
Author(s):  
E. Gloaguen ◽  
B. de Courcy ◽  
J.-P. Piquemal ◽  
J. Pilmé ◽  
O. Parisel ◽  
...  

1992 ◽  
Vol 70 (7) ◽  
pp. 1971-1977 ◽  
Author(s):  
Nick Henry Werstiuk ◽  
George Timmins ◽  
Jiangong Ma ◽  
Timothy A. Wildman

A redetermination of the ultraviolet photoelectron (pe) spectrum of (Z)-2-methyl-1,3-pentadiene has led to a correction of the published spectrum. By studying (Z)-2-methyl-1,3,-pentadiene (1a) and (E)-2-methyl-1,3-pentadiene (1b) with MMX, MNDO, AM1, and abinitio MO computational methods and pe spectroscopy, we have shown that a combination of these methods provides useful insights on the conformational behaviour of methyl-substituted 1,3-dienes in the gas phase. Synthetic pe spectra, derived from the computed potential energy surfaces and angle-dependent orbital energies, are in good agreement with experiment. Thus, the E isomer prefers the s-trans conformer but the Z isomer prefers twisted s-cis conformations in the gas phase.


1967 ◽  
Vol 47 (1) ◽  
pp. 331-332 ◽  
Author(s):  
Roger P. Blickensderfer ◽  
George E. Ewing

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