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  Synthesis and membrane binding properties of a lipopeptide fragment from influenza virus A hemagglutinin

Eisele, F., Kuhlmann, J., & Waldmann, H. (2002). Synthesis and membrane binding properties of a lipopeptide fragment from influenza virus A hemagglutinin. Chemistry - A European Journal, 8(15):, pp. 3362-3376. Retrieved from http://dx.doi.org/10.1002/1521-3765(20020802)8:15<3362:AID-CHEM3362>3.0.CO;2-0.

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資料種別: 学術論文
その他のタイトル : Chem.-Eur. J.

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 作成者:
Eisele, Frank, 著者
Kuhlmann, Jürgen1, 著者           
Waldmann, Herbert2, 著者           
所属:
1Sonstige Wissenschaftliche Organisationseinheiten, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753294              
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              

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キーワード: enzyme catalysis; hemagglutinin; lipidated peptides; peptides; protecting groups
 要旨: Hemagglutinin from influenza virus A is a S-palmitoylated lipoglycoprotein in which the lipid groups are thought to influence the interaction between cell membrane and capsid during budding of viral offspring as well as fusion processes of the viral membrane with the endosome after entry of the viral particle into the cell. The paper describes the development of a method for the synthesis of characteristic lipidated hemagglutinin derived peptides which additionally carry the fluorescent 7-nitrobenz-2oxa-1,3-diazole (NBD) group. To achieve this goal the enzyme-sensitive para- phenylacetoxybenzyloxycarbonyl (PAOB) ester was developed. It is cleaved from the peptides and lipidated peptides under very mild conditions and with complete selectivity by treatment with the enzyme penicillin G acylase; this results in the formation of a phenolate. This intermediate spontaneously undergoes fragmentation thereby releasing the desired carboxylates. The combined use of this enzymelabile fragmenting ester with the acidlabile Boc group, the Pd-0-sensitive allyl ester and the corresponding Aloc urethane gave access to a mono-S- palmitoylated and a doubly S-palmitoylated NBD-labelled hemagglutinin peptide. The binding of these lipopeptides to model membranes was analyzed in a biophysical setup monitoring the transfer of fluorescent-labelled lipopeptide from vesicles containing the non-ex-changeable fluorescence quencher Rho-DHPE to quencher-free vesicles. The experiments demonstrate that one lipid group is not sufficient for quasi-irreversible membrane insertion of lipidated peptides. This is, however, achieved by introduction of the bis-palmitoyl anchor. The intervesicle transfer always implies release of peptides localized at the outer face of the vesicles into solution followed by diffusion to and insertion into acceptor vesicles. For peptides bound at the inner face of the vesicle membrane, however, an additional flip-flop diffusion to the outer face has to occur beforehand. The kinetics of these processes were estimated by fast chemical quench of the outside fluorophores by sodium dithionite.

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言語: eng - English
 日付: 2002-08-01
 出版の状態: 出版
 ページ: -
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 査読: 査読あり
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出版物 1

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出版物名: Chemistry - A European Journal
  出版物の別名 : Chem.-Eur. J.
種別: 学術雑誌
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出版社, 出版地: -
ページ: - 巻号: 8 (15) 通巻号: 1 開始・終了ページ: 3362 - 3376 識別子(ISBN, ISSN, DOIなど): -