Keller B, Bickle T A
Gene. 1986;49(2):245-51. doi: 10.1016/0378-1119(86)90285-4.
We have sequenced gene 21 coding for the bacteriophage T4 prohead protease. The sequence codes for a protein of 212 amino acids (aa) with an Mr of 23,251. A second possible in-frame initiation site was also found which would code for an Mr 18,440 protein. Evidence is presented that this second site is used in vivo. The only striking homology of gp21 to other proteins is with the serine proteases. The protein is homologous to a short aa sequence around the active site, but has a His where the active site Ser is normally found. However, mutation of this His to Ser gave a functional protein that could not be inhibited by serine protease inhibitors. We have located three sites in the gene that give rise to temperature-sensitive mutations. One of these is towards the N-terminus of the gene, the other two flank the region that shows homology with serine proteases. Attempts to overproduce the protein in Escherichia coli failed due to the extreme lability of the enzyme. A frame-shift mutation in the gene was therefore constructed which allowed the synthesis of large amounts of a stable N-terminal fragment of the protein.
我们已对编码噬菌体T4原头部蛋白酶的基因21进行了测序。该序列编码一个由212个氨基酸(aa)组成、分子量为23,251的蛋白质。还发现了第二个可能的框内起始位点,它将编码一个分子量为18,440的蛋白质。有证据表明这个第二个位点在体内被使用。gp21与其他蛋白质唯一显著的同源性是与丝氨酸蛋白酶的同源性。该蛋白质与活性位点周围的一段短氨基酸序列同源,但在通常为活性位点丝氨酸的位置有一个组氨酸。然而,将这个组氨酸突变为丝氨酸产生了一种不能被丝氨酸蛋白酶抑制剂抑制的功能性蛋白质。我们在该基因中定位了三个导致温度敏感突变的位点。其中一个位于基因的N端附近,另外两个位于与丝氨酸蛋白酶显示同源性的区域两侧。由于该酶的极度不稳定性,在大肠杆菌中过量生产该蛋白质的尝试失败了。因此构建了该基因中的一个移码突变,使得能够合成大量稳定的该蛋白质的N端片段。