Design of New Antimicrobials

描述(申请人提供)：许多对传统抗生素产生抗药性的相关细菌菌株的戏剧性和不断增加的出现，现在是人类健康的一个主要问题。由于经典抗生素在临床上的广泛应用，已经出现了抗生素耐药性。因此，在最好的情况下，抗生素的药效正在逐渐下降；在最坏的情况下，出现了无法治疗的感染的激增，例如多重耐药结核病和耐万古霉素的肠球菌菌株。因此，在美国，通过延长住院时间和日益积极的治疗来治疗医院感染的成本估计已上升到300亿美元。因此，采用新型抗生素是有经济动机的。此外，必须应对生物恐怖主义的威胁，即能够轻易地设计出对人类造成致命后果的新细菌菌株。与现有的抗生素相比，抗菌肽作为一种全新的抗生素结构类别显示出巨大的潜力，既有新的作用模式，也有不同的细胞靶点。对唯一靶标为细胞膜的膜活性多肽的抗药性不会出现，因为这将需要微生物细胞膜的脂组成发生重大变化。阳离子抗菌肽的优势在于它们能够迅速杀死目标细胞，它们不同寻常的广谱活性，以及它们对一些临床分离的更严重的抗生素耐药病原体的活性。抗菌肽作为抗生素使用的主要障碍是它们对真核细胞的毒性或裂解能力。我们采用了通过单一的L和D-氨基酸取代来系统改变两类不同抗菌肽的两亲性、疏水性和结构的方法。通过这种方法，我们能够将抗真核细胞的活性从抗微生物活性中分离出来，即增加抗菌活性，并显著降低或消除对正常细胞的毒性(通过溶血活性来衡量)。我们在两种不同结构的抗菌肽中发现了先导化合物，14个残基的环状2-片肽和26个残基的1-螺旋肽具有作为广谱抗生素的临床潜力。这两类化合物的同时开发将最快地促进我们对这些多肽的作用机制和对微生物膜选择性的共同要求的了解。我们需要进一步优化我们从头设计的先导化合物，以确保我们在保持高治疗指数的同时获得最佳的抗菌活性。关键问题：1)哪种类型的正电荷残基是增强环状2-折叠和1-螺旋多肽的特异性的最佳类型；2)选择了最好的正电荷残基后，我们能否在保持较高的治疗指数的同时增加疏水性以提高抗菌活性；3)证明我们的多肽对一系列人类细胞无毒；4)通过结构测定(固体核磁共振)显示我们的两类抗菌肽在膜上的位置；5)在两个动物模型中证明我们的多肽对铜绿假单胞菌的挑战具有体内效果；6)将我们的研究扩展到其他严重细菌感染的动物模型。项目叙事 对传统抗生素产生抗药性的许多相关菌株的戏剧性和不断增加的出现，现在是人类健康的一个主要问题。由于经典抗生素在临床上的广泛应用，已经出现了抗生素耐药性。因此，在美国，通过延长住院时间和日益积极的治疗来治疗医院感染的成本估计已上升到300亿美元。因此，采用新型抗生素有经济动机。7.项目叙事 许多相关品系的戏剧性和不断增加的出现 对传统抗生素产生抗药性的细菌现在是人类健康的一个主要问题。 由于经典抗生素在临床上的广泛应用，已经出现了抗生素耐药性。 因此，通过延长治疗医院感染的费用 住院治疗和日益积极的治疗估计已上升到300亿美元 因此，在美国，采用新型抗生素是有经济动机的。

DESCRIPTION (provided by applicant): The dramatic and ever-increasing emergence of many relevant strains of bacteria resistant to traditional antibiotics is now a major issue in human health. Antibiotic resistance has arisen due to the extensive clinical use of classical antibiotics. Thus, at best, antibiotics are progressively demonstrating decreased efficacy; at worst, there has been an upsurge of untreatable infections, such as multi-resistant tuberculosis and vancomycin-resistant Enterococcus strains. Consequently, the cost of treating nosocomial infections through extended hospitalization and increasingly aggressive therapy has risen to an estimated $30 billion in the U.S. Therefore, there is an economic incentive to adopt novel antibiotics. In addition, the threat of bioterrorism, that is the ability to easily engineer new strains of bacteria with deadly consequences to humans, must be dealt with. Compared to existing antibiotics, antimicrobial peptides show great potential as a radically new structural class of antibiotics, with both novel modes of action as well as different cellular targets. The development of resistance to membrane active peptides whose sole target is the cytoplasmic membrane is not expected since this would require substantial changes in the lipid composition of cell membranes of microorganisms. The advantages of cationic antimicrobial peptides are their ability to kill target cells rapidly, their unusual broad spectrum activity and their activity against some of the more serious antibiotic-resistant pathogens isolated in clinics. The major barrier to the use of antimicrobial peptides as antibiotics has been their toxicity or ability to lyse eukaryotic cells. We have taken an approach of systematic alteration in the amphipathicity, hydrophobicity and structure of two different classes of antimicrobial peptides by single L- and D- amino acid substitutions. With this approach we were able to dissociate anti-eukaryotic activity from antimicrobial activity, i.e. increase the antimicrobial activity and dramatically reduce or eliminate toxicity to normal cells (as measured by hemolytic activity). We have discovered lead compounds in two different structural classes of antimicrobial peptides, a 14-residue cyclic 2-sheet peptide and a 26-residue 1-helical peptide with clinical potential as broad spectrum antibiotics. The simultaneous development of both classes of compounds will most rapidly advance our knowledge of the mechanism of action of these peptides and the common requirements for selectivity for microbial membranes. Further optimization of our de novo designed lead compounds is required to ensure we obtain the best antimicrobial activity while maintaining a high therapeutic index. Key questions: 1) which is the best type of positively-charged residue in the center of the non-polar face to enhance specificity on the cyclic 2- sheet and 1-helical peptides; 2) having selected the best positively-charged residue can we increase hydrophobicity to improve antimicrobial activity while maintaining a high therapeutic index; 3) demonstrate that our peptides are non-toxic to a series of human cell lines; 4) to show by structural determination (solid-state NMR) the location of our two classes of antimicrobial peptides in the membrane; 5) demonstrate in vivo efficacy of our peptides against Pseudomonas aeruginosa challenge in two animal models; 6) extend our studies to animal models of other serious bacterial infections.7. Project Narrative The dramatic and ever-increasing emergence of many relevant strains of bacteria resistant to traditional antibiotics is now a major issue in human health. Antibiotic resistance has arisen due to the extensive clinical use of classical antibiotics. Consequently, the cost of treating nosocomial infections through extended hospitalization and increasingly aggressive therapy has risen to an estimated $30 billion in the U.S. Thus, there is an economic incentive to adopt novel antibiotics. 7. Project Narrative The dramatic and ever-increasing emergence of many relevant strains of bacteria resistant to traditional antibiotics is now a major issue in human health. Antibiotic resistance has arisen due to the extensive clinical use of classical antibiotics. Consequently, the cost of treating nosocomial infections through extended hospitalization and increasingly aggressive therapy has risen to an estimated $30 billion in the U.S. Thus, there is an economic incentive to adopt novel antibiotics.