Fincham A G, Hu Y Y, Lau E, Pavlova Z, Slavkin H C, Snead M L
Department of Basic Sciences (Biochemistry), University of Southern California, Los Angeles 90033.
Calcif Tissue Int. 1990 Aug;47(2):105-11. doi: 10.1007/BF02555993.
A strategy based on high pressure liquid chromatography (HPLC) techniques for the isolation or a principal amelogenin molecule from a single human dentition is described. A partial sequence (33 residues) for this 24 kDa amelogenin is presented and related to earlier studies of human 5 kDa tyrosine-rich amelogenin polypeptides (TRAPs). A failure to identify amino acid residue #25 (tryptophan in other amelogenins) suggests that this 24 kDa amelogenin is the progenitor of the human TRAP-2 molecule and provides further support for the possibility of several human amelogenin gene products, generated by splice-junction selection, from the single amelogenin gene in the same individual. Alternatively, multiple amelogenins may arise by expression of both the AMELX and AMELY loci.
本文描述了一种基于高压液相色谱(HPLC)技术从单个人类牙列中分离主要釉原蛋白分子的策略。给出了这种24 kDa釉原蛋白的部分序列(33个残基),并与早期对人类5 kDa富含酪氨酸的釉原蛋白多肽(TRAPs)的研究相关。未能鉴定出第25位氨基酸残基(其他釉原蛋白中的色氨酸)表明,这种24 kDa釉原蛋白是人类TRAP - 2分子的前体,并进一步支持了同一个体中单个釉原蛋白基因通过剪接连接选择产生几种人类釉原蛋白基因产物的可能性。或者,多个釉原蛋白可能通过AMELX和AMELY基因座的表达产生。