L-Alanine, L-lysyl-L-lysyl-L-alanyl-L-leucyl-L-leucyl-L-alanyl-L-leucyl-L-alanyl-L-leucyl-L-histidyl-L-histidyl-L-leucyl-L-alanyl-L-histidyl-L-leucyl-L-alanyl-L-leucyl-L-histidyl-L-leucyl-L-alanyl-L-leucyl-L-alanyl-L-leucyl-L-lysyl-L-lysyl-

L-Alanine, L-lysyl-L-lysyl-L-alanyl-L-leucyl-L-leucyl-L-alanyl-L-leucyl-L-alanyl-L-leucyl-L-histidyl-L-histidyl-L-leucyl-L-alanyl-L-histidyl-L-leucyl-L-alanyl-L-leucyl-L-histidyl-L-leucyl-L-alanyl-L-leucyl-L-alanyl-L-leucyl-L-lysyl-L-lysyl- Chemische Eigenschaften,Einsatz,Produktion Methoden

• Beschreibung

  LAH4 is an antimicrobial peptide that strongly interacts with phospholipid membranes, exhibiting in vitro transfection efficiency.

  LAH4 exhibits potent antimicrobial, nucleic acid transfection and cell penetration activities[1]. LAH4 mediates the transport of functional β-galactosidase, a large tetrameric protein of about 0.5 MDa, into the cell interior[2]. At acidic pH, LAH4 has exhibited a high tendency to interact strongly with and be adsorbed on anionic membrane[3].

• Einzelnachweise

  [1]. Perrone B, et al. Lipid interactions of LAH4, a peptide with antimicrobial and nucleic acid transfection activities. Eur Biophys J. 2014 Nov;43(10-11):499-507. [2]. Moulay G, et al. Histidine-rich designer peptides of the LAH4 family promote cell delivery of a multitude of cargo. J Pept Sci. 2017 Apr;23(4):320-328. [3]. Islami M, et al. Study of orientation and penetration of LAH4 into lipid bilayer membranes: pH and composition dependence. Chem Biol Drug Des. 2014 Aug;84(2):242-52.

L-Alanine, L-lysyl-L-lysyl-L-alanyl-L-leucyl-L-leucyl-L-alanyl-L-leucyl-L-alanyl-L-leucyl-L-histidyl-L-histidyl-L-leucyl-L-alanyl-L-histidyl-L-leucyl-L-alanyl-L-leucyl-L-histidyl-L-leucyl-L-alanyl-L-leucyl-L-alanyl-L-leucyl-L-lysyl-L-lysyl- Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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