Literature DB >> 7691661

Human alpha 2-macroglobulin structure. Location of Cys-949 residues within a half-molecule measured by fluorescence energy transfer.

P G Gettins1, B C Crews.   

Abstract

To localize the pair of thiol-ester-derived cysteine-949 residues within a half-molecule of alpha 2M and estimate the internal diameter of this alpha 2-macroglobulin trap, we have measured the separation between these cysteines. We unexpectedly found that the two cysteines of intermediate form alpha 2M had different reactivity, which permitted selective modification of one cysteine with dansyl, and the other with fluorescein fluorophores. From fluorescence energy transfer measurements, we calculated a separation of 41 +/- 10 A between these fluorophores. This indicates that the Cys-949 residues are probably located at the perimeter of the trap with an internal diameter at least as large as this separation.

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Year:  1993        PMID: 7691661     DOI: 10.1016/0014-5793(93)80633-6

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  1 in total

1.  Characterization of the interaction between alpha2-macroglobulin and fibroblast growth factor-2: the role of hydrophobic interactions.

Authors:  Smitha Mathew; Sanja Arandjelovic; Wayne F Beyer; Steven L Gonias; Salvatore V Pizzo
Journal:  Biochem J       Date:  2003-08-15       Impact factor: 3.857

  1 in total

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