Matsuoka Tsuneyoshi, Tomita Shunsuke, Hamada Hiroyuki, Shiraki Kentaro
Institute of Applied Physics, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, Japan.
J Biosci Bioeng. 2007 May;103(5):440-3. doi: 10.1263/jbb.103.440.
An additive that is highly effective in small amounts for controlling protein inactivation and aggregation has long been demanded. In this paper we show amidated amino acids as new potent additives. In the presence of 100 mM amidated amino acids, e.g., Ala, Arg, Asn, Met, and Val, the heat-induced inactivation and aggregation of lysozyme at pH 7.1 are one order of magnitude slower than those in the absence of additives. Although a high Arg concentration (>1 M) has been used to prevent aggregation among amino acids, it is worth mentioning that above amidated amino acids can prevent aggregation at submolar concentrations. The data obtained suggest the importance of amino and amide groups rather than the guanidium group as an aggregation suppressor.
长期以来,人们一直需要一种在少量情况下就能高效控制蛋白质失活和聚集的添加剂。在本文中,我们展示了酰胺化氨基酸作为新型高效添加剂。在存在100 mM酰胺化氨基酸(例如丙氨酸、精氨酸、天冬酰胺、甲硫氨酸和缬氨酸)的情况下,pH 7.1时溶菌酶的热诱导失活和聚集比没有添加剂时慢一个数量级。虽然高浓度的精氨酸(>1 M)已被用于防止氨基酸之间的聚集,但值得一提的是,上述酰胺化氨基酸在亚摩尔浓度下就能防止聚集。所获得的数据表明,作为聚集抑制剂,氨基和酰胺基比胍基更重要。