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The Use of a Free Peptide for Preparation of a C-Terminal Building Block for Polypeptide Synthesis in Combination with a Peptide Thioester

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Book cover Peptides: The Wave of the Future

Part of the book series: American Peptide Symposia ((APSY,volume 7))

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Abstract

We report herein a new strategy for the synthesis of polypeptides using recombinant proteins (non-protected peptides) in combination with S-alkyl peptide thioesters (peptide thioesters) [1, 2] for the use as building blocks.

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Authors and Affiliations

  1. Institute for Protein Research, Osaka University, Osaka, 565-0871, Japan

    Saburo Aimoto, Kenta Teruya, Koki Hasegawa, Kenichi Akaji & Toru Kawakami

Authors
  1. Saburo Aimoto
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  2. Kenta Teruya
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  3. Koki Hasegawa
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  4. Kenichi Akaji
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  5. Toru Kawakami
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Editor information

Editors and Affiliations

  1. Spyder Instruments, Inc. and Illumina, Inc., 9885 Towne Centre Drive, 92121, San Diego, CA, USA

    Michal Lebl

  2. Torrey Pines Institute for Molecular Studies, Mixture Sciences, Inc., 3550 General Atomics Court, 92121, San Diego, CA, USA

    Richard A. Houghten

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© 2001 Springer Science+Business Media Dordrecht

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Aimoto, S., Teruya, K., Hasegawa, K., Akaji, K., Kawakami, T. (2001). The Use of a Free Peptide for Preparation of a C-Terminal Building Block for Polypeptide Synthesis in Combination with a Peptide Thioester. In: Lebl, M., Houghten, R.A. (eds) Peptides: The Wave of the Future. American Peptide Symposia, vol 7. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-0464-0_49

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  • DOI: https://doi.org/10.1007/978-94-010-0464-0_49

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-3905-5

  • Online ISBN: 978-94-010-0464-0

  • eBook Packages: Springer Book Archive

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