Open AccessThe Role of Propeptide in the Refolding of Human Group IB Phospholipase A<sub>2</sub>
Author(s) -
Hong-Qiang Cheng,
Gen-Jun Xu
Publication year - 2004
Publication title -
acta biochimica et biophysica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.771
H-Index - 57
eISSN - 1745-7270
pISSN - 1672-9145
DOI - 10.1093/abbs/36.9.583
Subject(s) - zymogen , chemistry , enzyme , phospholipase a2 , phospholipase a , disulfide bond , biochemistry , phospholipase , yield (engineering) , materials science , metallurgy
Human group IB phospholipase A2 (IB-PLA2) and its zymogen (proIB-PLA2) were purified from E.coli. Refolding was carried out by diluting the denatured forms of both IB-PLA2 and proIB-PLA2 with renaturation buffer in which the disulfide bonds were completely reduced. The refolding yield of proIB-PLA2 was increased by about 50% over that of the mature enzyme. The refolding of IB-PLA2 usually produced aggregates under normal conditions, as determined by light scattering. In addition, the unfolding experiments showed that the mature enzyme was more stable than the proenzyme toward denaturants in the presence of DTT. Results suggested that the N-terminal sequence rather than its conformation of human proIB-PLA2 played an important role in the refolding process.