Kim J S, Raines R T
Department of Biochemistry, University of Wisconsin, Madison 53706-1569.
Protein Sci. 1993 Mar;2(3):348-56. doi: 10.1002/pro.5560020307.
S-peptide (residues 1-20) and S-protein (residues 21-124) are the enzymatically inactive products of the limited digestion of ribonuclease A by subtilisin. S-peptide binds S-protein with high affinity to form ribonuclease S, which has full enzymatic activity. Recombinant DNA technology was used to produce a fusion protein having three parts: carrier, spacer, and target. The two carriers used were the first 15 residues of S-peptide (S15) and a mutant S15 in which Asp 14 had been changed to Asn (D14N S15). The spacer consisted of three proline residues and a four-residue sequence recognized by factor Xa protease. The target was beta-galactosidase. The interaction between the S-peptide portion of the fusion protein and immobilized S-protein allowed for affinity purification of the fusion protein under denaturing (S15 as carrier) or nondenaturing (D14N S15 as carrier) conditions. A sensitive method was developed to detect the fusion protein after sodium dodecyl sulfate-polyacrylamide gel electrophoresis by its ribonuclease activity following activation with S-protein. S-peptide has distinct advantages over existing carriers in fusion proteins in that it combines a small size (> or = 15 residues), a tunable affinity for ligand (Kd > or = 10(-9) M), and a high sensitivity of detection (> or = 10(-16) mol in a gel).
S肽(1 - 20位氨基酸残基)和S蛋白(21 - 124位氨基酸残基)是枯草杆菌蛋白酶对核糖核酸酶A进行有限消化后的无酶活性产物。S肽与S蛋白以高亲和力结合形成具有完整酶活性的核糖核酸酶S。利用重组DNA技术制备了一种由三部分组成的融合蛋白:载体、间隔区和靶标。所使用的两种载体分别是S肽的前15个氨基酸残基(S15)和将第14位天冬氨酸突变为天冬酰胺的突变型S15(D14N S15)。间隔区由三个脯氨酸残基和一个能被Xa因子蛋白酶识别的四氨基酸序列组成。靶标是β - 半乳糖苷酶。融合蛋白中S肽部分与固定化S蛋白之间的相互作用使得在变性条件下(以S15为载体)或非变性条件下(以D14N S15为载体)都能对融合蛋白进行亲和纯化。开发了一种灵敏的方法,在十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳后,通过用S蛋白激活后的核糖核酸酶活性来检测融合蛋白。与融合蛋白中现有的载体相比,S肽具有明显优势,它兼具小尺寸(≥15个氨基酸残基)、对配体的亲和力可调节(解离常数Kd≥10⁻⁹ M)以及检测灵敏度高(凝胶中≥10⁻¹⁶ mol)的特点。