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交联生长激素二聚体具有增强的生物活性。

Cross-linked growth hormone dimers have enhanced biological activity.

作者信息

Mockridge J W, Aston R, Morrell D J, Holder A T

机构信息

The Babraham Institute, Babraham, Cambridge, UK.

出版信息

Eur J Endocrinol. 1998 Apr;138(4):449-59. doi: 10.1530/eje.0.1380449.

Abstract

In this study we have investigated the effect on the bioactivity of pituitary-derived human growth hormone (hGH) and recombinant bovine (b) GH after the addition of various concentrations of the water soluble cross-linking agent 1-ethyl-3(3-dimethylaminopropyl) carbodiimide (EDC; 6.25-100 mg/ml). The biological activity of resulting cross-linked reactions were determined by its ability to promote incorporation of 35SO4(2-) into costal cartilage of hypopituitary Snell dwarf mice in vivo. Administration of EDC-treated hGH solutions resulted in a significant enhancement of hormone activity in vivo compared with non-cross-linked samples. A similar significant enhancement of bGH activity in vivo was also observed when solutions containing recombinant bGH were cross-linked using EDC. For both hGH and bGH the degree of enhancement appears to be dose-dependent for the concentration of EDC (6.25-100 mg/ml for hGH; 6.25-50 mg/ml for bGH) present in the cross-linking reactions. SDS-PAGE analysis of EDC cross-linked solutions containing hGH and bGH spiked with 125I-hGH and 125I-bGH respectively revealed that dimeric GH was the primary cross-linked component. Increasing the concentration of EDC in cross-linking reactions resulted in increased formation of dimeric hGH and bGH. There was a significant correlation between the amount of GH dimer present and the increase in biological activity, suggesting that GH dimers were responsible for the enhanced biological activity. This was confirmed by the enhanced biological activity of a purified preparation of EDC cross-linked dimeric hGH. In conclusion, covalently cross-linked GH dimers reported here have enhanced bioactivity in vivo. However, since naturally occurring GH dimers are known to have reduced biological activity, this work suggests that the structure of EDC cross-linked GH dimers differs fundamentally from that of native dimeric hGH.

摘要

在本研究中,我们研究了添加不同浓度的水溶性交联剂1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC;6.25 - 100 mg/ml)后,对垂体来源的人生长激素(hGH)和重组牛生长激素(bGH)生物活性的影响。通过其促进35SO4(2-)掺入垂体功能减退的斯内尔侏儒小鼠肋软骨的能力,来测定所得交联反应的生物活性。与未交联的样品相比,给予EDC处理的hGH溶液在体内导致激素活性显著增强。当使用EDC对含有重组bGH的溶液进行交联时,在体内也观察到bGH活性有类似的显著增强。对于hGH和bGH,增强程度似乎与交联反应中存在的EDC浓度(hGH为6.25 - 100 mg/ml;bGH为6.25 - 50 mg/ml)呈剂量依赖性。分别用125I-hGH和125I-bGH加标的含有hGH和bGH的EDC交联溶液的SDS-PAGE分析表明,二聚体GH是主要的交联成分。增加交联反应中EDC的浓度会导致二聚体hGH和bGH的形成增加。存在的GH二聚体数量与生物活性的增加之间存在显著相关性,表明GH二聚体是生物活性增强的原因。纯化的EDC交联二聚体hGH制剂的增强生物活性证实了这一点。总之,本文报道的共价交联GH二聚体在体内具有增强的生物活性。然而,由于已知天然存在的GH二聚体生物活性降低,这项工作表明EDC交联GH二聚体的结构与天然二聚体hGH的结构有根本差异。

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