Dyson M R, Murray K
Institute of Cell and Molecular Biology, University of Edinburgh, Scotland.
Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):2194-8. doi: 10.1073/pnas.92.6.2194.
As an example for studies of contacts involved in complex biological systems, peptide ligands that bind to the core antigen of hepatitis B virus (HBcAg) have been selected from a random hexapeptide library displayed on filamentous phage. Affinity-purified phage bearing aa sequence LLGRMK, or some related sequences, bound full-length or truncated HBcAg but did not bind denatured HBcAg. The long (L), but not the short (S), hepatitis B virus envelope polypeptide, when synthesized in an in vitro system, bound firmly to HBcAg, indicating that interaction between HBcAg and the pre-S region of the L polypeptide is critical for virus morphogenesis. This interaction was inhibited by peptide ALLGRMKG, suggesting that this and related small molecules may inhibit viral assembly.
作为研究复杂生物系统中相关接触的一个例子,从丝状噬菌体展示的随机六肽文库中筛选出了与乙型肝炎病毒核心抗原(HBcAg)结合的肽配体。携带氨基酸序列LLGRMK或一些相关序列的亲和纯化噬菌体能够结合全长或截短的HBcAg,但不能结合变性的HBcAg。在体外系统中合成时,乙型肝炎病毒的长(L)包膜多肽而非短(S)包膜多肽能与HBcAg牢固结合,这表明HBcAg与L多肽前S区域之间的相互作用对病毒形态发生至关重要。这种相互作用被肽ALLGRMKG抑制,这表明该肽及相关小分子可能会抑制病毒组装。