Kokan-Moore N P, Bergdoll M S
Department of Food Microbiology and Toxicology, University of Wisconsin-Madison.
Rev Infect Dis. 1989 Jan-Feb;11 Suppl 1:S125-9.
The biologically active areas of toxic shock syndrome toxin 1 (TSST-1) were investigated using chemical fragmentation of the toxin with cyanogen bromide (CNBr). All three main CNBr-generated fragments of TSST-1, with estimated molecular weights of 20,000, 18,000, and 15,000, reacted with monoclonal antibodies (MAbs) 4T, 5T, 6T, 7T, 8T, and 9T, as determined by autoradiography. The epitopes involved in the mitogenic active site were located on the 15,000-Da internal fragment as determined by the neutralization of the mitogenic activity by the MAb. Modification of the methionine residues in the native TSST-1 by alkylation with iodoacetic acid had no effect on the serologic or mitogenic activity.
利用溴化氰(CNBr)对毒素进行化学裂解,研究了中毒性休克综合征毒素1(TSST-1)的生物活性区域。通过放射自显影测定,TSST-1的所有三个主要的由CNBr产生的片段,估计分子量分别为20,000、18,000和15,000,均与单克隆抗体(MAb)4T、5T、6T、7T、8T和9T发生反应。通过单克隆抗体对促有丝分裂活性的中和作用确定,参与促有丝分裂活性位点的表位位于15,000道尔顿的内部片段上。用碘乙酸烷基化对天然TSST-1中的甲硫氨酸残基进行修饰,对血清学或促有丝分裂活性没有影响。