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. 2000 Aug 1;19(15):3870–3875. doi: 10.1093/emboj/19.15.3870

Table II. Refolding time constants determined by reverse-phase HPLC for the disappearance of the fully reduced protein (R), the formation (τ1) and disappearance (τ2) of des-[76-94] and the formation of the native state (N) during refolding of fully reduced lysozyme. In addition the time constants obtained for the conversion of purified des-[76-94] to the native state are shown.

Protein species τ1 (min)
τ2 (min)
  –Ficoll +Ficoll –Ficoll +Ficoll
Ra 1.45 ± 0.04 1.09 ± 0.15
des-[76-94]a 16.8 ± 1.9 9.9 ± 1.6 209 ± 36 278 ± 45
Na 20.7 ± 2.5 15.7 ± 2.4 194 ± 50 265 ± 53
des-[76-94]b 264 ± 2 432 ± 14

Refolding was carried out in the absence and presence of 200 g/l Ficoll 70.

aRefolding kinetics determined during refolding from the fully reduced state.

bRefolding kinetics determined during refolding of purified des-[76-94].