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Kurouski, Dmitry, Van Duyne, Richard P., Lednev, Igor K. (2015) Exploring the structure and formation mechanism of amyloid fibrils by Raman spectroscopy: a review. The Analyst, 140 (15). 4967-4980 doi:10.1039/c5an00342c

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Reference TypeJournal (article/letter/editorial)
TitleExploring the structure and formation mechanism of amyloid fibrils by Raman spectroscopy: a review
JournalThe Analyst
AuthorsKurouski, DmitryAuthor
Van Duyne, Richard P.Author
Lednev, Igor K.Author
Year2015Volume140
Issue15
PublisherRoyal Society of Chemistry (RSC)
DOIdoi:10.1039/c5an00342cSearch in ResearchGate
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Mindat Ref. ID8205375Long-form Identifiermindat:1:5:8205375:6
GUID0
Full ReferenceKurouski, Dmitry, Van Duyne, Richard P., Lednev, Igor K. (2015) Exploring the structure and formation mechanism of amyloid fibrils by Raman spectroscopy: a review. The Analyst, 140 (15). 4967-4980 doi:10.1039/c5an00342c
Plain TextKurouski, Dmitry, Van Duyne, Richard P., Lednev, Igor K. (2015) Exploring the structure and formation mechanism of amyloid fibrils by Raman spectroscopy: a review. The Analyst, 140 (15). 4967-4980 doi:10.1039/c5an00342c
In(2015) The Analyst Vol. 140 (15) Royal Society of Chemistry (RSC)

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Kurouski, Dmitry, Lauro, William, Lednev, Igor K. (2010) Amyloid fibrils are “alive”: spontaneous refolding from one polymorph to another. Chemical Communications, 46 (24). 4249pp. doi:10.1039/b926758a
Kurouski, Dmitry, Van Duyne, Richard P. (2015) In SituDetection and Identification of Hair Dyes Using Surface-Enhanced Raman Spectroscopy (SERS). Analytical Chemistry, 87 (5). 2901-2906 doi:10.1021/ac504405u
Deckert-Gaudig, Tanja, Kurouski, Dmitry, Hedegaard, Martin A. B., Singh, Pushkar, Lednev, Igor K., Deckert, Volker (2016) Spatially resolved spectroscopic differentiation of hydrophilic and hydrophobic domains on individual insulin amyloid fibrils. Scientific Reports, 6. doi:10.1038/srep33575
Kurouski, Dmitry, Lombardi, Rosina A., Dukor, Rina K., Lednev, Igor K., Nafie, Laurence A. (2010) Direct observation and pH control of reversed supramolecular chirality in insulin fibrils by vibrational circular dichroism. Chemical Communications, 46 (38). 7154pp. doi:10.1039/c0cc02423f
Kurouski, Dmitry, Postiglione, Thomas, Deckert-Gaudig, Tanja, Deckert, Volker, Lednev, Igor K. (2013) Amide I vibrational mode suppression in surface (SERS) and tip (TERS) enhanced Raman spectra of protein specimens. The Analyst, 138 (6). 1665pp. doi:10.1039/c2an36478f
Xu, Ming, Shashilov, Victor, Lednev, Igor K. (2007) Probing the Cross-β Core Structure of Amyloid Fibrils by Hydrogen−Deuterium Exchange Deep Ultraviolet Resonance Raman Spectroscopy. Journal Of The American Chemical Society, 129 (36) 11002-11003 doi:10.1021/ja073798w
Kurouski, Dmitry, Lu, Xuefang, Popova, Ludmila, Wan, William, Shanmugasundaram, Maruda, Stubbs, Gerald, Dukor, Rina K., Lednev, Igor K., Nafie, Laurence A. (2014) Is Supramolecular Filament Chirality the Underlying Cause of Major Morphology Differences in Amyloid Fibrils?. Journal Of The American Chemical Society, 136 (6) 2302-2312 doi:10.1021/ja407583r
Kurouski, Dmitry, Handen, Joseph D., Dukor, Rina K., Nafie, Laurence A., Lednev, Igor K. (2015) Supramolecular chirality in peptide microcrystals. Chemical Communications, 51 (1). 89-92 doi:10.1039/c4cc05002a
Shashilov, Victor, Xu, Ming, Makarava, Natallia, Savtchenko, Regina, Baskakov, Ilia V., Lednev, Igor K. (2012) Dissecting Structure of Prion Amyloid Fibrils by Hydrogen–Deuterium Exchange Ultraviolet Raman Spectroscopy. The Journal of Physical Chemistry B, 116 (27). 7926-7930 doi:10.1021/jp2122455
Jiang, Nan, Kurouski, Dmitry, Pozzi, Eric A., Chiang, Naihao, Hersam, Mark C., Van Duyne, Richard P. (2016) Tip-enhanced Raman spectroscopy: From concepts to practical applications. Chemical Physics Letters, 659. 16-24 doi:10.1016/j.cplett.2016.06.035
Shanmugasundaram, Maruda, Kurouski, Dmitry, Wan, William, Stubbs, Gerald, Dukor, Rina K., Nafie, Laurence A., Lednev, Igor K. (2015) Rapid Filament Supramolecular Chirality Reversal of HET-s (218–289) Prion Fibrils Driven by pH Elevation. The Journal of Physical Chemistry B, 119 (27). 8521-8525 doi:10.1021/acs.jpcb.5b04779
 
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