The Cys-949 residues of alpha 2-macroglobulin are likely located at the perimeter of the trap, with an internal diameter at least 41 +/- 10 A.
Refines alpha 2-macroglobulin trap model in experimental systems; leaves open relevance to human protease regulation.
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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Gettins et al. (1993) studied this question.
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