Thannhauser T W, Scheraga H A
Cornell Center of Advanced Technology in Biotechnology, Cornell University, Ithaca, New York 14853-2703, USA.
J Protein Chem. 1996 Nov;15(8):751-3. doi: 10.1007/BF01887149.
The state of aggregation of recombinant desulfatohirudin (r-HV1) in solution under physiological conditions (pH 7.5, 0.15 N NaCl) was investigated by sedimentation equilibrium. The weight-average molecular weight MW determined by sedimentation equilibrium was found to be 6914 +/- 76 Da compared to 6964 Da expected from the amino acid sequence. The MZ/MW ratio was found to be 1.03, which demonstrates that under the conditions studied hirudin exists in solution as a monomer. This result is in agreement with the relative molecular weight (M,) of recombinant hirudin variant 3 reported by Otto and Seckler [(1991), Eur. J. Biochem. 202, 67-73], who also used equilibrium ultracentrifugation, but not with the molecular weight estimated from gel permeation chromatography of natural hirudin (51,300 Da) [Konno et al. (1988), Arch. Biochem. Biophys. 267, 158-166]. Knowledge of the state of aggregation is essential for understanding the mechanism of interaction of thrombin and hirudin under physiological conditions.
在生理条件(pH 7.5,0.15 N NaCl)下,采用沉降平衡法研究了重组去硫酸水蛭素(r-HV1)在溶液中的聚集状态。通过沉降平衡测定的重均分子量MW为6914 +/- 76 Da,而根据氨基酸序列预期的分子量为6964 Da。发现Mz/MW比为1.03,这表明在所研究的条件下水蛭素在溶液中以单体形式存在。该结果与Otto和Seckler [(1991),Eur. J. Biochem. 202, 67 - 73]报道的重组水蛭素变体3的相对分子量(M,)一致,他们也使用了平衡超速离心法,但与通过天然水蛭素的凝胶渗透色谱法估计的分子量(51,300 Da)[Konno等人(1988),Arch. Biochem. Biophys. 267, 158 - 166]不一致。聚集状态的知识对于理解生理条件下凝血酶和水蛭素的相互作用机制至关重要。