McClements W, Yamanaka G, Garsky V, Perry H, Bacchetti S, Colonno R, Stein R B
Department of Virus and Cell Biology Research, Merck Sharp and Dohme Research Laboratories, West Point, Pennsylvania 19486.
Virology. 1988 Jan;162(1):270-3. doi: 10.1016/0042-6822(88)90421-7.
It has recently been reported that a nonapeptide (H-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu-OH) identical in sequence to the last nine amino acid residues of RR2, the small subunit of herpes simplex virus (HSV) ribonucleotide reductase (E.C. 1.17.4.1; RR), can inhibit HSV RR activity in vitro. It has been postulated that this peptide acts by interfering with the interaction of the large subunit, RR1, and RR2, but direct demonstration of its mechanism of action has not been reported. We present data which show that the inhibition of HSV RR by this oligopeptide is due to induced subunit dissociation.
最近有报道称,一种九肽(H-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu-OH),其序列与单纯疱疹病毒(HSV)核糖核苷酸还原酶(E.C. 1.17.4.1;RR)的小亚基RR2的最后九个氨基酸残基相同,在体外可抑制HSV RR活性。据推测,该肽通过干扰大亚基RR1和RR2的相互作用发挥作用,但尚未有其作用机制的直接证据报道。我们提供的数据表明,这种寡肽对HSV RR的抑制作用是由于诱导亚基解离所致。