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Karas JA, Noor A, Schieber C, et al. The efficient synthesis and purification of amyloid-β(1-42) using an oligoethylene glycol-containing photocleavable lysine tag. Chem Commun (Camb). 2017;53(51):6903-6905doi: 10.1039/c7cc03147e.
Karas, J. A., Noor, A., Schieber, C., Connell, T. U., Separovic, F., & Donnelly, P. S. (2017). The efficient synthesis and purification of amyloid-β(1-42) using an oligoethylene glycol-containing photocleavable lysine tag. Chemical communications (Cambridge, England), 53(51), 6903-6905. https://doi.org/10.1039/c7cc03147e
Karas, John A, et al. "The efficient synthesis and purification of amyloid-β(1-42) using an oligoethylene glycol-containing photocleavable lysine tag." Chemical communications (Cambridge, England) vol. 53,51 (2017): 6903-6905. doi: https://doi.org/10.1039/c7cc03147e
Karas JA, Noor A, Schieber C, Connell TU, Separovic F, Donnelly PS. The efficient synthesis and purification of amyloid-β(1-42) using an oligoethylene glycol-containing photocleavable lysine tag. Chem Commun (Camb). 2017 Jun 22;53(51):6903-6905. doi: 10.1039/c7cc03147e. PMID: 28607975.
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Chem Commun (Camb). 2017 Jun 22;53(51):6903-6905. doi: 10.1039/c7cc03147e.

The efficient synthesis and purification of amyloid-β(1-42) using an oligoethylene glycol-containing photocleavable lysine tag.

Chemical communications (Cambridge, England)

John A Karas, Asif Noor, Christine Schieber, Timothy U Connell, Frances Separovic, Paul S Donnelly

Affiliations

  1. School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, VIC 3010, Australia. [email protected] [email protected] and Department of Chemical and Biomolecular Engineering, The University of Melbourne, VIC 3010, Australia.
  2. School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, VIC 3010, Australia. [email protected] [email protected].

PMID: 28607975 DOI: 10.1039/c7cc03147e

Abstract

A short, monodisperse oligoethylene glycol-containing photocleavable lysine tag was developed to facilitate the efficient purification of hydrophobic and fibril-forming peptides. This new tag was used to prepare a modified Aβ

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