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基于聚-L-谷氨酸的炭疽毒素强效抑制剂的合成

Synthesis of potent inhibitors of anthrax toxin based on poly-L-glutamic acid.

作者信息

Joshi Amit, Saraph Arundhati, Poon Vincent, Mogridge Jeremy, Kane Ravi S

机构信息

The Howard P. Isermann Department of Chemical and Biological Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.

出版信息

Bioconjug Chem. 2006 Sep-Oct;17(5):1265-9. doi: 10.1021/bc060042y.

Abstract

We report the synthesis of biodegradable polyvalent inhibitors of anthrax toxin based on poly-L-glutamic acid (PLGA). These biocompatible polyvalent inhibitors are at least 4 orders of magnitude more potent than the corresponding monovalent peptides in vitro and are comparable in potency to polyacrylamide-based inhibitors of anthrax toxin assembly. We have elucidated the influence of peptide density on inhibitory potency and demonstrated that these inhibitory potencies are limited by kinetics, with even higher activities seen when the inhibitors are preincubated with the heptameric receptor-binding subunit of anthrax toxin prior to exposure to cells. These polyvalent inhibitors are also effective at neutralizing anthrax toxin in vivo and represent attractive leads for designing biocompatible anthrax therapeutics.

摘要

我们报道了基于聚-L-谷氨酸(PLGA)的可生物降解的炭疽毒素多价抑制剂的合成。这些生物相容性多价抑制剂在体外的效力比相应的单价肽至少高4个数量级,并且在效力上与基于聚丙烯酰胺的炭疽毒素组装抑制剂相当。我们阐明了肽密度对抑制效力的影响,并证明这些抑制效力受动力学限制,当抑制剂在暴露于细胞之前与炭疽毒素的七聚体受体结合亚基预孵育时,能观察到更高的活性。这些多价抑制剂在体内也能有效中和炭疽毒素,是设计生物相容性炭疽治疗药物的有吸引力的先导物。

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