Watson Judy J, Fahey Mark S, van den Worm Edwin, Engels Ferdi, Nijkamp Frans P, Stroemer Paul, McMahon Steve, Allen Shelley J, Dawbarn David
Molecular Neurobiology Unit, Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, Bristol, UK.
J Pharmacol Exp Ther. 2006 Mar;316(3):1122-9. doi: 10.1124/jpet.105.095844. Epub 2005 Nov 11.
Elevated levels of nerve growth factor have been linked to the onset and persistence of many pain-related disorders and asthma. Described here are the design, expression, refolding, and purification of a monomeric (nonstrand-swapped) form of the binding domain of the nerve growth factor receptor, designated TrkAd5. We have shown that TrkAd5 produced recombinantly binds nerve growth factor with picomolar affinity. TrkAd5 has been characterized using a variety of biophysical and biochemical assays and is shown here to be stable in both plasma and urine. The palliative effects of TrkAd5 are demonstrated in animal models of inflammatory pain and allergic asthma. We conclude that TrkAd5 will prove effective in ameliorating both acute and chronic conditions where nerve growth factor acts as a mediator and suggest a role for its application in vivo as a novel therapeutic.
神经生长因子水平升高与许多疼痛相关疾病和哮喘的发病及持续存在有关。本文描述了神经生长因子受体结合域的单体(非链交换)形式TrkAd5的设计、表达、重折叠和纯化。我们已经证明,重组产生的TrkAd5以皮摩尔亲和力结合神经生长因子。已使用多种生物物理和生化分析方法对TrkAd5进行了表征,结果表明它在血浆和尿液中均稳定。TrkAd5在炎性疼痛和过敏性哮喘的动物模型中显示出缓解作用。我们得出结论,TrkAd5将被证明在改善神经生长因子作为介质的急性和慢性病症方面有效,并表明其在体内作为一种新型治疗方法的应用前景。