Literature DB >> 3407916

Purification of a hydrophobic surfactant peptide using high-performance liquid chromatography.

P Arjomaa1, M Hallman.   

Abstract

A 4- to 6-kDa hydrophobic peptide (SP4-6) was purified from human pulmonary surfactant. Sep Pak Florisil cartridges removed most of the lipids and the 18-kDa peptide. Analytical wide-pore reversed-phase HPLC column separated a single peptide that contained no detectable lipids (less than 1 nmol/2.5 micrograms protein). N-terminal analysis indicated that this peptide was pure, but the N-terminal amino acid was blocked. The peptide was capable of restoring the in vitro surface properties of synthetic phospholipids, which is characteristic of native lung surfactant.

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Year:  1988        PMID: 3407916     DOI: 10.1016/0003-2697(88)90143-1

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  3 in total

1.  Thermodynamic effects of the hydrophobic surfactant proteins on the early adsorption of pulmonary surfactant.

Authors:  V Schram; S B Hall
Journal:  Biophys J       Date:  2001-09       Impact factor: 4.033

2.  Surfactant protein composition of lamellar bodies isolated from rat lung.

Authors:  M A Oosterlaken-Dijksterhuis; M van Eijk; B L van Buel; L M van Golde; H P Haagsman
Journal:  Biochem J       Date:  1991-02-15       Impact factor: 3.857

3.  SP-B and SP-C alter diffusion in bilayers of pulmonary surfactant.

Authors:  Vincent Schram; Stephen B Hall
Journal:  Biophys J       Date:  2004-06       Impact factor: 4.033

  3 in total

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