Davis J M, Boswell B A, Bächinger H P
Research Unit, Shriners Hospital for Crippled Children, Portland, Oregon 97201.
J Biol Chem. 1989 May 25;264(15):8956-62.
Intact, monomeric type IV procollagen was isolated from the medium of PF-HR9 cells. Its stability was measured by optical rotatory dispersion, differential scanning calorimetry, and trypsin susceptibility of the partially unfolded molecules. At neutral pH, a complex transition between 35 and 42 degrees C and a smaller transition at 48 degrees C are observed by optical rotatory dispersion, using a heating rate of 10 degrees C/h. Reduction of the heating rate to 1.6 degrees C/h resulted in a 1 degree C lowering of the apparent melting temperatures. A similar curve is observed in 10 mM acetic acid, with transitions about 2 degrees C lower. Differential scanning calorimetry revealed transitions at 36.0, 42.1, and 48.0 degrees C at neutral pH, with a total transition enthalpy of 17.1 kJ/mol tripeptide units. In 10 mM acetic acid, transitions at 35.6, 38.9, 41.7, and 50.0 degrees C are observed. The transition enthalpy is 16.4 kJ/mol tripeptide units. The transition enthalpy is similar to values found for interstitial collagens. Results from trypsin digestion experiments are consistent with the stability found by optical methods and calorimetry. The rate and completeness of refolding after melting were measured. In neutral buffer, the initial rate was found to be 0.041 min-1, faster than the refolding rates observed with types pN III and III collagen. Peptidyl prolyl cis-trans-isomerase increased the refolding rate to 0.083 min-1, indicating that cis-trans-isomerization is the rate-limiting step, despite the interruptions in the triple helix. Trypsin digestion experiments indicated that the refolding mechanism is similar in the presence and absence of the enzyme. Refolding was nearly complete in neutral buffer. In 10 mM acetic acid, folding was considerably slower and went to about 74% completion. In both solvents, the refolded material was only slightly less stable than the native material. Electron microscopy of partially refolded samples showed that most refolding started at the COOH terminus, but some was initiated at other sites.
完整的单体Ⅳ型前胶原是从PF-HR9细胞的培养基中分离出来的。通过旋光色散、差示扫描量热法以及部分展开分子的胰蛋白酶敏感性来测定其稳定性。在中性pH条件下,以10℃/h的升温速率进行旋光色散测定时,观察到在35至42℃之间有一个复杂的转变,在48℃时有一个较小的转变。将升温速率降至1.6℃/h会导致表观解链温度降低1℃。在10 mM乙酸中观察到类似的曲线,转变温度约低2℃。差示扫描量热法显示在中性pH条件下,转变温度分别为36.0、42.1和48.0℃,三肽单元的总转变焓为17.1 kJ/mol。在10 mM乙酸中,观察到转变温度为35.6、38.9、41.7和50.0℃。转变焓为16.4 kJ/mol三肽单元。该转变焓与间质胶原的值相似。胰蛋白酶消化实验的结果与通过光学方法和量热法测得的稳定性一致。测定了熔化后重折叠的速率和完整性。在中性缓冲液中,初始速率为0.041 min-1,比观察到的pN III型和III型胶原的重折叠速率快。肽基脯氨酰顺反异构酶将重折叠速率提高到0.083 min-1,表明尽管三螺旋中有中断,但顺反异构化是限速步骤。胰蛋白酶消化实验表明,在有酶和无酶的情况下重折叠机制相似。在中性缓冲液中重折叠几乎完全。在10 mM乙酸中,折叠要慢得多,完成度约为74%。在两种溶剂中,重折叠后的材料稳定性仅略低于天然材料。对部分重折叠样品的电子显微镜观察表明,大多数重折叠从COOH末端开始,但也有一些在其他位点起始。