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  • P-ISSN 2233-4203
  • E-ISSN 2093-8950

Oligomer Complexes of the (VQIVYK + NNQQNY) and (VQIVYK + LYQLEN) Mixing Solutions

Mass Spectrometry Letters / Mass Spectrometry Letters, (P)2233-4203; (E)2093-8950
2019, v.10 no.1, pp.32-37
https://doi.org/10.5478/MSL.2019.10.1.32
Jung Yeon-Ji (Department of Applied Chemistry, Kumoh National In)
Shin Min-Ji (Department of Applied Chemistry, Kumoh National Institute of Technology)
Kim Ho-Tae (Department of Applied Chemistry, Kumoh National Institute of Technology)
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Abstract

The π-π interactions of the peptide-dimer and peptide-trimer complexes were investigated in the (VQIVYK + LYQLEN) and (VQIVYK + NNQQNY) mixing solutions. The results showed that tyrosine (Y) residues were critical in the for-mation of hetero peptide-dimers and -trimers during the early oligomerization process. We used collision-induced dissociation (CID) along with electrospray ionization mass spectroscopy (ESI-MS) to obtain the structural information of the hetero-dimers and -trimers. We chose three amyloidogenic peptides–VQIVYK, NNQQNY, and LYQLEN–from tau protein, yeast prion-like protein Sup35, and insulin chain A, respectively. Hetero-dimer, -trimer, -tetramer, and -pentamer complexes were observed in the mass spectra. The tandem mass spectrum of the hetero-dimer and hetero-trimer showed two different fragmentation patterns (covalent and non-covalent bond dissociation). Y-Y interaction structures were also proposed for the hetero-dimer and -trimer complexes.

keywords
Peptide oligomer, VQIVYK, NNQQNY, LYQLEN, mass spectrometry (MS), MS/MS


Reference

1

Haass, C.. (2007). . J. Nat. Rev. Mol. Cell Biol, 8, 101-.

2

Eisenberg, D.. (2006). . Acc. Chem. Res, 39, 568-.

3

Sawaya, M. R.. (2007). . Nature, 447, 453-.

4

Nelson, R. (2005). . Nature, 435, 773-.

5

Cohen, A. S. (1959). . Nature, 183, 1202-.

6

Diaz-Avalos, R. (2003). . J. Mol. Biol, 330, 1165-.

7

Balbirnie, M. (2001). . Proc. Natl. Acad. Sci, 98, 2375-.

8

Plumley, J. A. (2010). . J. Am. Chem. Soc, 132, 1758-.

9

Lin, Y.-F. (2009). . Biopolymers, 94, 269-.

10

Vaden, T. D. (2008). . J. Am. Chem. Soc, 130, 14640-.

11

Caplan, M. R. (2000). . Biomacromolecules, 1, 627-.

12

Lopez de la Paz, M. (2002). . Proc. Natl. Acad. Sci, 99, 16052-.

13

Porat, Y. (2004). . Biochemistry, 43, 14454-.

14

Gazit, E.. (2002). . FASEB J. Off. Publ. Fed. Am. Soc. Exp. Biol, 16, 77-.

15

Azriel, R. (2001). . J. Biol. Chem, 276, 34156-.

16

McGaughey, G. B.. (1998). . J. Biol. Chem, 273, 15458-.

17

Jang, H.-S. (2014). . Nature Commun, 5, 3665-.

18

Zhao, R. (2017). . Mol. Phys, 2017, 1400697-.

19

Zhao, J.-H. (2010). . Mol. Simul, 36, 1013-.

20

Sievers, S. A. (2011). . Nature, 475, 96-.

21

Do, T. D. (2013). . J. Phys. Chem. B, 117, 8436-.

22

Zhao, J.-H. (2013). . J. Mol. Model., 19, 151-.

23

Lin, Y.-F. (2011). . J. Taiwan Inst. Chem. Eng., 42, 394-.

24

Seo, J.-H. (2017). . Int. J. Mass Spec, 415, 55-.

25

Seo, J.-H. (2018). . Chem. Phys. Lett, 708, 61-.

26

Azriel, R. (2001). . J. Biol. Chem, 276, 34156-.

27

Porat, Y. (2004). . Biochem, 43, 14454-.

28

Porat, Y. (2003). . Biopolymers, 69, 161-.

Submission Date
2018-12-17
Revised Date
2019-01-19
Accepted Date
2019-01-22
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