Shigenaga T, Takayenoki Y, Kawasaki S, Seki N, Muta T, Toh Y, Ito A, Iwanaga S
Department of Molecular Biology, Graduate School of Medical Science, Fukuoka.
J Biochem. 1993 Sep;114(3):307-16. doi: 10.1093/oxfordjournals.jbchem.a124173.
We designed a method for separating two types of granules, a smaller (S) but dense and a larger (L) but less dense granule from hemocytes of the horseshoe crab (Tachypleus tridentatus), using continuous sucrose density gradient centrifugation. The isolated L-granules contained at least three clotting factors plus a clottable protein, coagulogen, as the major component. The known anti-lipopolysaccharide factor and 7 additional unknown protein components were also present in the L-granules. Two known natural substrates, Pro-rich protein and 8.6 kDa protein, for limulus transglutaminase [Tokunaga, F., Yamada, M., Miyata, T., Ding, Y.-L., Hiranaga-Kawabata, M., Muta, T., Iwanaga, S., Ichinose, A., & Davie, E.W. (1993) J. Biol. Chem. 268, 252-261] were present in the L-granules. On the other hand, the isolated S-granules contained antimicrobial tachyplesins I and II (17 amino acids in length) as the major component, in addition to 6 unidentified proteins with molecular masses of less than 30 kDa. The structural analyses of tachyplesin analogs indicated that all these peptides of mature form are stored in the S-granules, together with a processing intermediate containing the COOH-terminal Gly-Lys sequence. We also found an Arg-rich protein of 22 kDa and a Leu-rich protein of 30 kDa in S-granules. Based on these observations, we speculate that protein components in L-granules, which probably contain all the factors essential for the limulus clotting system, participate in immobilization of invading microbes and that factors in the S-granules containing tachyplesins contribute to a self-defense system against invaders.
我们设计了一种方法,通过连续蔗糖密度梯度离心从中国鲎(Tachypleus tridentatus)的血细胞中分离出两种颗粒,一种较小(S)但致密,另一种较大(L)但密度较小。分离出的L颗粒含有至少三种凝血因子以及一种可凝结蛋白——凝固蛋白原作为主要成分。已知的抗脂多糖因子和另外7种未知蛋白质成分也存在于L颗粒中。L颗粒中还存在两种已知的鲎转谷氨酰胺酶的天然底物,富含脯氨酸的蛋白质和8.6 kDa蛋白质[德永,F.,山田,M.,宫田,T.,丁,Y.-L.,平永川端,M.,武田,T.,岩永,S.,市野濑,A.,& 戴维,E.W.(1993年)《生物化学杂志》268,252 - 261]。另一方面,分离出的S颗粒除了含有6种分子量小于30 kDa的未鉴定蛋白质外,还含有抗菌肽鲎素I和II(长度为17个氨基酸)作为主要成分。鲎素类似物的结构分析表明,所有这些成熟形式的肽都与含有COOH末端甘氨酸 - 赖氨酸序列的加工中间体一起储存在S颗粒中。我们还在S颗粒中发现了一种22 kDa的富含精氨酸的蛋白质和一种30 kDa的富含亮氨酸的蛋白质。基于这些观察结果,我们推测L颗粒中的蛋白质成分可能包含鲎凝血系统所需的所有因子,参与入侵微生物的固定,而含有鲎素的S颗粒中的因子有助于抵御入侵者的自我防御系统。