Literature DB >> 12296715

Direct observation of the multistep helix formation of poly-L-glutamic acids.

Tetsunari Kimura1, Satoshi Takahashi, Shuji Akiyama, Takanori Uzawa, Koichiro Ishimori, Isao Morishima.   

Abstract

The helix formation dynamics of poly-L-glutamic acids (PGAs) were observed by the microsecond-resolved Fourier transform infrared (FTIR) and circular dichroism (CD) spectroscopies. The helix formation of 34-residue PGA from random coil at pH (or pD for FTIR) 8.0 was initiated by a pH jump to 4.9 using the rapid solution mixer whose mixing dead time is 50 micros. The amide I' line in the time-resolved FTIR spectra exhibited the fast (<100 micros) increase of the total helical content. The time-resolved CD spectra of the same process also showed the fast (<150 micros) formation of short helical segments (5 +/- 1 residues), which was followed by the slower (<1 ms) elongation of the short helices to longer helices (>10 residues). Similar dynamics were observed for the same pH jump of approximately 190-residue PGA, although there were additional steps that made the helix formation of approximately 190-residue PGA more complex. The observed multistep helix formation is likely caused by the strong hydrogen-bonding interactions between the protonated side chains of PGAs.

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Year:  2002        PMID: 12296715     DOI: 10.1021/ja026639f

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  18 in total

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8.  Revealing Fast Structural Dynamics in pH-Responsive Peptides with Time-Resolved X-ray Scattering.

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Journal:  J Phys Chem B       Date:  2019-02-27       Impact factor: 2.991

9.  Exposing the Nucleation Site in α-Helix Folding: A Joint Experimental and Simulation Study.

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10.  Unfolding of α-helical 20-residue poly-glutamic acid analyzed by multiple runs of canonical molecular dynamics simulations.

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Journal:  PeerJ       Date:  2018-05-15       Impact factor: 2.984

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