Bonato C, Eng J, Hulmes J D, Miedel M, Pan Y C, Yalow R S
Peptides. 1986 Jul-Aug;7(4):689-93. doi: 10.1016/0196-9781(86)90045-8.
Heptadecapeptide gastrins (G17) have been purified and sequenced from a variety of species. However, progastrin (G34) sequences have been determined only for pig and human from purified peptides and for rat from cDNA. Since G34 in most species accounts for only approximately 5% of total antral gastrin, micropurification techniques must be employed to avoid the need for large quantities of antral tissue. Efficient purification methodology yielded 1.5 and 1.3 nmol of G34 from the antrum of a single goat and of a single dog, respectively. The N-terminal pyroglutamyl residues were enzymatically removed and the peptides were sequenced through to the proximity of their COOH-termini. The COOH-terminal sequences of goat and dog G34 were confirmed by sequencing the corresponding deblocked G17 from each animal. The previously published dog G17 sequence was shown to be incorrect. The sequences for dog and goat G34 are: Dog less than ELGLQGPPQLVADLSKKQGPWMEEEEAAYGWMDF# Goat less than ELGLQDPPHMVADLSKKQGPWVEEEEAAYGWMDF# Dog and goat gastrins differ in 3 sites in the 17 amino acid NH2-terminus and only a single site in G17 (the sites of differences are underlined). The ratio for sulfated to non-sulfated antral G17 is 9:1 for the goat and 1:9 for the dog.
十七肽胃泌素(G17)已从多种物种中纯化并测序。然而,前胃泌素(G34)的序列仅在猪和人类中通过纯化肽段确定,在大鼠中则通过cDNA确定。由于大多数物种中的G34仅占胃窦胃泌素总量的约5%,因此必须采用微纯化技术以避免需要大量的胃窦组织。高效的纯化方法分别从一只山羊和一只狗的胃窦中获得了1.5和1.3 nmol的G34。N端焦谷氨酰残基通过酶法去除,肽段测序至其COOH末端附近。通过对每只动物相应的去封闭G17进行测序,证实了山羊和狗G34的COOH末端序列。先前发表的狗G17序列被证明是错误的。狗和山羊G34的序列如下:狗:小于ELGLQGPPQLVADLSKKQGPWMEEEEAAYGWMDF# 山羊:小于ELGLQDPPHMVADLSKKQGPWVEEEEAAYGWMDF# 狗和山羊胃泌素在17个氨基酸的NH2末端有3个位点不同,在G17中只有1个位点不同(不同位点已加下划线)。山羊胃窦G17的硫酸化与非硫酸化比例为9:1,狗为1:9。