Direct observation of the multistep helix formation of poly-L-glutamic acids
- PMID: 12296715
- DOI: 10.1021/ja026639f
Direct observation of the multistep helix formation of poly-L-glutamic acids
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.
Similar articles
-
Stability and folding dynamics of polyglutamic acid.Eur Biophys J. 2011 May;40(5):673-85. doi: 10.1007/s00249-011-0673-8. Epub 2011 Jan 28. Eur Biophys J. 2011. PMID: 21274709
-
[Study on the pH-sensitive secondary structure of gamma-PGA embedded with magnetite nanoparticles].Guang Pu Xue Yu Guang Pu Fen Xi. 2009 Aug;29(8):2148-51. Guang Pu Xue Yu Guang Pu Fen Xi. 2009. PMID: 19839327 Chinese.
-
Bifurcated hydrogen bonds stabilize fibrils of poly(L-glutamic) acid.J Phys Chem B. 2010 Jun 24;114(24):8278-83. doi: 10.1021/jp102440n. J Phys Chem B. 2010. PMID: 20509699
-
Spiral superstructures of amyloid-like fibrils of polyglutamic acid: an infrared absorption and vibrational circular dichroism study.J Phys Chem B. 2011 Sep 22;115(37):11010-6. doi: 10.1021/jp206271e. Epub 2011 Aug 29. J Phys Chem B. 2011. PMID: 21842891
-
Biomolecular dynamics studied with IR-spectroscopy using quantum cascade lasers combined with nanosecond perturbation techniques.Spectrochim Acta A Mol Biomol Spectrosc. 2017 Jun 15;181:192-199. doi: 10.1016/j.saa.2017.03.053. Epub 2017 Mar 23. Spectrochim Acta A Mol Biomol Spectrosc. 2017. PMID: 28364666
Cited by
-
Exposing the Nucleation Site in α-Helix Folding: A Joint Experimental and Simulation Study.J Phys Chem B. 2019 Feb 28;123(8):1797-1807. doi: 10.1021/acs.jpcb.8b12220. Epub 2019 Feb 14. J Phys Chem B. 2019. PMID: 30694671 Free PMC article.
-
Structural basis for the transcriptional regulation of heme homeostasis in Lactococcus lactis.J Biol Chem. 2012 Aug 31;287(36):30755-68. doi: 10.1074/jbc.M112.370916. Epub 2012 Jul 13. J Biol Chem. 2012. PMID: 22798069 Free PMC article.
-
Amyloid oligomer conformation in a group of natively folded proteins.PLoS One. 2008 Sep 18;3(9):e3235. doi: 10.1371/journal.pone.0003235. PLoS One. 2008. PMID: 18800165 Free PMC article.
-
Dehydration of main-chain amides in the final folding step of single-chain monellin revealed by time-resolved infrared spectroscopy.Proc Natl Acad Sci U S A. 2008 Sep 9;105(36):13391-6. doi: 10.1073/pnas.0801316105. Epub 2008 Aug 29. Proc Natl Acad Sci U S A. 2008. PMID: 18757727 Free PMC article.
-
Revealing Fast Structural Dynamics in pH-Responsive Peptides with Time-Resolved X-ray Scattering.J Phys Chem B. 2019 Mar 7;123(9):2016-2021. doi: 10.1021/acs.jpcb.9b00072. Epub 2019 Feb 27. J Phys Chem B. 2019. PMID: 30763085 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources