Literature DB >> 7810899

Conformational changes in the reversed phase liquid chromatography of recombinant human growth hormone as a function of organic solvent: the molten globule state.

S Wicar1, M G Mulkerrin, G Bathory, L H Khundkar, B L Karger.   

Abstract

As a continuation of a previous paper on the retention behavior of recombinant human growth hormone (rhGH) in reversed phase chromatography at pH 6.5 (Oroszlan, P., et al. Anal. Chem. 1992, 64, 1623-1631) the effect of 1-propanol (1-PrOH) and acetonitrile on the conformation of rhGH at this pH has been investigated by circular dichroism (CD), second-derivative UV spectroscopy, fluorescence anisotropy, fluorescence quenching, and fluorescence lifetime measurements. Addition of 1-PrOH up to a concentration of 10% (v/v) does not cause any significant changes in protein structure. However, above this concentration, a transition from the native to a new state is observed; the transition is completed above 30% (v/v) of 1-PrOH, the composition for completion being dependent on temperature. This change in structure correlates with retention changes observed in reversed phase chromatography. The new rhGH conformation retains much of the alpha-helicity and possesses a slightly expanded hydrodynamic radius relative to native rhGH. Second-derivative UV spectroscopy suggests that the hydrogen bond between Trp 86 and Asp 169, spanning two alpha-helices, remains intact. On the other hand, the near-UV CD intensity changes from positive to negative in the Trp region of the spectrum, signaling an alteration in the Trp environment. In addition, fluorescence quenching measurements with trichloroethanol reveal greater accessibility to solvent of the Trp residue after the conformational transition has occurred. From the results, it is concluded that a molten globule state (compact state retaining much of the secondary structure of the native state but with a disrupted tertiary structure) is produced with the addition of > 30% (v/v) 1-PrOH.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7810899     DOI: 10.1021/ac00094a011

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  6 in total

1.  Temperature- and pH-induced multiple partially unfolded states of recombinant human interferon-alpha2a: possible implications in protein stability.

Authors:  Vikas K Sharma; Devendra S Kalonia
Journal:  Pharm Res       Date:  2003-11       Impact factor: 4.200

2.  Human Growth Hormone Adsorption Kinetics and Conformation on Self-Assembled Monolayers.

Authors:  Jos Buijs; David W Britt; Vladimir Hlady
Journal:  Langmuir       Date:  1998-01-20       Impact factor: 3.882

3.  Stable formulations of recombinant human growth hormone and interferon-gamma for microencapsulation in biodegradable microspheres.

Authors:  J L Cleland; A J Jones
Journal:  Pharm Res       Date:  1996-10       Impact factor: 4.200

4.  Non-native intermediate conformational states of human growth hormone in the presence of organic solvents.

Authors:  Muppalla Sukumar; Sacha M Storms; Michael R De Felippis
Journal:  Pharm Res       Date:  2005-05-17       Impact factor: 4.200

5.  Adsorption Kinetics, Conformation, and Mobility of the Growth Hormone and Lysozyme on Solid Surfaces, Studied with TIRF

Authors: 
Journal:  J Colloid Interface Sci       Date:  1997-06-01       Impact factor: 8.128

6.  Thermodynamic characterization of an intermediate state of human growth hormone.

Authors:  I Gomez-Orellana; B Variano; J Miura-Fraboni; S Milstein; D R Paton
Journal:  Protein Sci       Date:  1998-06       Impact factor: 6.725

  6 in total

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