Volume 10, Issue 2 pp. 81-88
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STUDIES ON CYTOCHROME C:

XII. Synthesis of the Protected Undecapeptide (Sequence 66–76) and Pentadecapeptide (Sequence 66–80) of Horse Heart Cytochrome c*

Luis Moroder

Luis Moroder

Centro di Studi sui Biopolimeri del C.N.R., Istituto di Chimica Organica dell'Università di Padova, Padova, Italy

Max-Plank-Institut für Biochemie, Abteilung Peptidchemie, Shillerstr. 42 D-8000 - München 2

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Gianfranco Borin

Gianfranco Borin

Centro di Studi sui Biopolimeri del C.N.R., Istituto di Chimica Organica dell'Università di Padova, Padova, Italy

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Bruno Filippi

Bruno Filippi

Centro di Studi sui Biopolimeri del C.N.R., Istituto di Chimica Organica dell'Università di Padova, Padova, Italy

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Diego Stivanello

Diego Stivanello

Centro di Studi sui Biopolimeri del C.N.R., Istituto di Chimica Organica dell'Università di Padova, Padova, Italy

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Fernando Marchiori

Corresponding Author

Fernando Marchiori

Centro di Studi sui Biopolimeri del C.N.R., Istituto di Chimica Organica dell'Università di Padova, Padova, Italy

Institute of Organic Chemistry University of Padova Via Marzolo, 1 35100 - Padova ItalySearch for more papers by this author
First published: August 1977
Citations: 5

The amino acid residues, except glycine, are of the L-configuration. For a simpler description the customary L-designation for individual amino acid residues is omitted. Standard abbreviations for amino acid derivatives and peptides are used according to the suggestion of the IUPAC-IUB Commission on Biochemical Nomenclature (1972) Biochemistry 11, 1726–1732.

Abstract

This paper is part of a series on synthesis of suitably protected peptides covering the 66–104 sequence of horse heart cytochrome c. It describes the preparation, by conventional procedures, of a partially protected Nα-benzyloxycarbonyl-undecapeptide hydrazide corresponding to the sequence from 66 to 76 (Fragment F), which represents a building block for the synthesis of the entire 66 – 104 sequence.

Moreover, the preparation is described of a partially protected pentadecapeptide corresponding to the sequence region 66 to 80, which represents the key peptide for the semisynthesis of the same COOH-terminal sequence utilizing the natural 81 – 104 N-trifluoroacetylated CNBr fragment.

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