Hunkapiller M W, Hood L E
Biochemistry. 1978 May 30;17(11):2124-33. doi: 10.1021/bi00604a016.
We have combined the use of a nonprotein carrier (Polybrene), high pressure liquid chromatography, and modifications in Edman chemistry with the improvements of a commercial spinning cup sequenator suggested by Wittmann-Liebold [Wittmann-Liebold, B. (1973) Hoppe-Seyler's Z. Physiol. Chem. 354, 1415] to analyze amino acid phenylthiohydantoins obtained from automated Edman degradation of microquantities of polypeptide directly without the use of radiolabel. This approach has allowed us to determine the sequence of the N-terminal 47 residues of sperm whale myoglobin starting with 200 pmol of protein, 77 residues of an antibody light chain with 5 nmole of protein, and 54 residues of an antibody heavy chain with 8 nmol of protein. In addition, we completely sequenced a hydrophobic 14-residue peptide at the 1.5-nmol level. Our technique of direct analysis for microsamples is capable of providing routine, extende N-terminal sequence analysis for nanomole and subnanomole levels of polypeptides and protines, and it also is applicable to analysis of more classical sample quantities.
我们将非蛋白质载体(聚凝胺)的使用、高压液相色谱法、埃德曼化学法的改进与维特曼 - 利博尔德[维特曼 - 利博尔德,B.(1973年)《霍普 - 赛勒生理化学杂志》354卷,1415页]建议的商用旋转杯测序仪的改进相结合,以分析直接从微量多肽的自动埃德曼降解中获得的氨基酸苯硫代乙内酰脲,而无需使用放射性标记。这种方法使我们能够从200皮摩尔的蛋白质开始确定抹香鲸肌红蛋白N端47个残基的序列,从5纳摩尔的蛋白质确定抗体轻链的77个残基,从8纳摩尔的蛋白质确定抗体重链的54个残基。此外,我们在1.5纳摩尔水平上完全测定了一个14个残基的疏水性肽段的序列。我们的微量样品直接分析技术能够为纳摩尔和亚纳摩尔水平的多肽和蛋白质提供常规的、扩展的N端序列分析,并且它也适用于更经典样品量的分析。