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蜂毒肽可能通过与核苷二磷酸激酶相互作用,间接激活HL-60细胞膜中Gi蛋白的GTP水解。

Mastoparan may activate GTP hydrolysis by Gi-proteins in HL-60 membranes indirectly through interaction with nucleoside diphosphate kinase.

作者信息

Klinker J F, Hagelüken A, Grünbaum L, Heilmann I, Nürnberg B, Harhammer R, Offermanns S, Schwaner I, Ervens J, Wenzel-Seifert K

机构信息

Institut für Pharmakologie, Freie Universität Berlin, Germany.

出版信息

Biochem J. 1994 Dec 1;304 ( Pt 2)(Pt 2):377-83. doi: 10.1042/bj3040377.

Abstract

The wasp venom, mastoparan (MP), activates reconstituted pertussis toxin (PTX)-sensitive G-proteins in a receptor-independent manner. We studied the effects of MP and its analogue, mastoparan 7 (MP 7), on G-protein activation in HL-60 cells and a reconstituted system and on nucleoside diphosphate kinase (NDPK)-catalysed GTP formation. MP activated high-affinity GTP hydrolysis in HL-60 membranes with an EC50 of 1-2 microM and a maximum at 10 microM. Unlike the effects of the formyl peptide receptor agonist, N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMet-Leu-Phe), on GTPase, those of MP were only partially PTX-sensitive. MP-induced rises in cytosolic Ca2+ concentration and superoxide-anion formation in intact HL-60 cells were also only incompletely PTX-sensitive. N-Ethylmaleimide inhibited MP-stimulated GTP hydrolysis to a greater extent than that stimulated by fMet-Leu-Phe. Unlike the latter, MP did not enhance incorporation of GTP azidoanilide into, and cholera toxin-catalysed ADP-ribosylation of, Gi-protein alpha-subunits in HL-60 membranes. By contrast to fMet-Leu-Phe, MP did not or only weakly stimulated binding of guanosine 5'-[gamma-thio]triphosphate to Gi-protein alpha-subunits. MP 7 was considerably more effective than MP at activating the GTPase of reconstituted Gi/G(o)-proteins, whereas in HL-60 membranes, MP and MP 7 were similarly effective. MP and MP 7 were similarly effective at activating [3H]GTP formation from [3H]GDP and GTP in HL-60 membranes and by NDPK purified from bovine liver mitochondria. Our data suggest the following: (1) MP activates Gi-proteins in HL-60 cells, but (2) the venom does not simply mimic receptor activation. (3) MP and MP 7 may activate GTP hydrolysis in HL-60 membranes indirectly through interaction with NDPK. (4) MP 7 is a more effective direct activator of PTX-sensitive G-proteins than MP, whereas with regard to NDPK, MP and MP 7 are similarly effective.

摘要

黄蜂毒液马斯托帕兰(MP)能以一种不依赖受体的方式激活重组百日咳毒素(PTX)敏感的G蛋白。我们研究了MP及其类似物马斯托帕兰7(MP 7)对HL - 60细胞和重组系统中G蛋白激活的影响,以及对核苷二磷酸激酶(NDPK)催化的GTP形成的影响。MP在HL - 60细胞膜中激活高亲和力GTP水解,其EC50为1 - 2微摩尔,在10微摩尔时达到最大值。与甲酰肽受体激动剂N - 甲酰 - L - 蛋氨酰 - L - 亮氨酰 - L - 苯丙氨酸(fMet - Leu - Phe)对GTP酶的作用不同,MP的作用仅部分对PTX敏感。MP诱导完整HL - 60细胞中胞质Ca2 +浓度升高和超氧阴离子形成也仅部分对PTX敏感。N - 乙基马来酰亚胺对MP刺激的GTP水解的抑制作用比对fMet - Leu - Phe刺激的抑制作用更大。与后者不同,MP不会增强GTP叠氮苯胺掺入HL - 60细胞膜中Gi蛋白α亚基以及霍乱毒素催化的Gi蛋白α亚基的ADP核糖基化。与fMet - Leu - Phe相反,MP不会或仅微弱刺激鸟苷5'-[γ - 硫代]三磷酸与Gi蛋白α亚基的结合。在激活重组Gi / G(o)蛋白的GTP酶方面,MP 7比MP有效得多,而在HL - 60细胞膜中,MP和MP 7效果相似。在HL - 60细胞膜中以及通过从牛肝线粒体纯化的NDPK,MP和MP 7在从[3H]GDP和GTP激活[3H]GTP形成方面效果相似。我们的数据表明:(1)MP在HL - 60细胞中激活Gi蛋白,但(2)该毒液并非简单地模拟受体激活。(3)MP和MP 7可能通过与NDPK相互作用间接激活HL - 60细胞膜中的GTP水解。(4)在激活PTX敏感的G蛋白方面,MP 7比MP是更有效的直接激活剂,而对于NDPK,MP和MP 7效果相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da5d/1137504/05506e757b6c/biochemj00074-0065-a.jpg

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