Pinilla C, Appel J R, Houghten R A
Torrey Pines Institute for Molecular Studies, San Diego, CA 92121.
Gene. 1993 Jun 15;128(1):71-6. doi: 10.1016/0378-1119(93)90155-v.
The use of synthetic peptide combinatorial libraries (SPCLs), each composed of tens of millions of peptides, is described here for the identification of bioactive peptides. The identification of optimal peptide sequences is achieved through the screening of SPCLs in solution, each element of which is composed of more than 10(5) nonsupport-bound peptides in approximately equimolar representation, along with an iterative synthesis and screening process. Using an SPCL composed in total of 52 128 400 nonacetylated hexapeptides, along with an iterative selection process based on competitive ELISA, we identified the antigenic determinant of beta-endorphin recognized by monoclonal antibody (mAb) 3E7. These results will be compared with the results found by others investigating mAb 3E7 using different peptide library approaches.
本文描述了合成肽组合文库(SPCLs)的使用,每个文库由数千万个肽组成,用于鉴定生物活性肽。通过在溶液中筛选SPCLs来确定最佳肽序列,其中每个元素由超过10⁵个非支持结合肽以近似等摩尔比例组成,同时还包括一个迭代合成和筛选过程。使用总共由52128400个非乙酰化六肽组成的SPCL,以及基于竞争性ELISA的迭代选择过程,我们鉴定出了单克隆抗体(mAb)3E7识别的β-内啡肽的抗原决定簇。这些结果将与其他使用不同肽库方法研究mAb 3E7的人所得到的结果进行比较。