Stuting H H, Krull I S
Department of Chemistry, Northeastern University, Boston, MA 02115.
J Chromatogr. 1991 Feb 8;539(1):91-109. doi: 10.1016/s0021-9673(01)95363-4.
The determination of molecular weight for pituitary and recombinant human growth hormone (p-hGH/Crescormon and r-hGH/Protropin) has been performed. This has involved on-line coupling of size-exclusion chromatography (SEC) and gradient elution, reversed-phase high-performance liquid chromatography (RP-HPLC) with low-angle laser light scattering (LALLS) detection. A 5-microns, 300 A, Delta-bond octyl column was used. Traditional specific refractive index increment (dn/dc) and refractive index (n) measurements have been performed in order to derive absolute weight-average molecular weight (Mw) information for p-hGH and r-hGH. Known concentrations of each protein have been separated using reversed-phase gradients utilizing acetonitrile with on-line LALLS determination of excess Rayleigh scattering factors. Accurate Mw data has been obtained for both proteins under conventional RP-HPLC gradient elution conditions. SEC data of both hGHs were found to be concentration, mobile phase, and column dependent for the particular analyses. Both medium- and high-resolution SEC-LALLS studies were performed, and all of these determinations further confirmed our RP-HPLC results. On-line LALLs provides certain advantages in identifying aggregates that may be present, even in medium-resolution SEC, where incomplete resolution occurs. The on-line coupling of modern RP-HPLC for biopolymers with LALLS detection represents a major step forward in the ability of bioanalytical chemists to determine the nature (monomer versus higher-order aggregate) of such materials. Other classes of biopolymers should prove suitable for studies with the same RP-HPLC-LALLS-UV approaches.
已对垂体来源和重组人生长激素(垂体来源人生长激素/Crescormon和重组人生长激素/Protropin)的分子量进行了测定。这涉及尺寸排阻色谱(SEC)与梯度洗脱、低角度激光光散射(LALLS)检测的反相高效液相色谱(RP-HPLC)的在线联用。使用了一根5微米、300埃的Delta键合辛基柱。为了获得垂体来源人生长激素和重组人生长激素的绝对重均分子量(Mw)信息,已进行了传统的比折光指数增量(dn/dc)和折射率(n)测量。每种蛋白质的已知浓度已通过使用乙腈的反相梯度进行分离,并在线通过LALLS测定过量瑞利散射因子。在常规RP-HPLC梯度洗脱条件下,已获得了两种蛋白质的准确Mw数据。发现两种人生长激素的SEC数据对于特定分析而言取决于浓度、流动相和色谱柱。进行了中分辨率和高分辨率的SEC-LALLS研究,所有这些测定进一步证实了我们的RP-HPLC结果。在线LALLS在识别可能存在的聚集体方面具有一定优势,即使在中分辨率SEC中出现不完全分离的情况下也是如此。现代生物聚合物RP-HPLC与LALLS检测的在线联用代表了生物分析化学家在确定此类材料的性质(单体与高阶聚集体)能力方面向前迈出的重要一步。其他类别的生物聚合物应证明适用于采用相同的RP-HPLC-LALLS-UV方法进行研究。