High Selective Performance of Designed Antibacterial and Anticancer Peptide Amphiphiles

抗菌活性 两亲性 细胞毒性 氨基酸 体外 体内 生物化学 生物物理学 细胞膜 三肽 细胞 细菌 生物 化学 共聚物 遗传学 聚合物 生物技术 有机化学
作者
Cuixia Chen,Yucan Chen,Cheng Yang,Ping Zeng,Hai Xu,Fang Pan,Jian R. Lu
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:7 (31): 17346-17355 被引量:88
标识
DOI:10.1021/acsami.5b04547
摘要

Short designed peptide amphiphiles are attractive at killing bacteria and inhibiting cancer cell growth, and the flexibility in their structural design offers a great potential for improving their potency and biocompatibility to mammalian host cells. Amino acid sequences such as G(IIKK)nI-NH2 (n≥3) have been shown to be membrane lytic, but terminal amino acid modifications could impose a huge influence on their performance. We report in this work how terminal amino acid modifications to G(IIKK)3I-NH2 influence its α-helical structure, membrane penetrating ability, and selective actions against different cell types. Deletion of an N-terminal Gly or a C-terminal Ile did not affect their antibacterial activity much, an observation consistent with their binding behavior to negatively charged membrane lipid monolayers. However, the cytotoxicity against mammalian cells was much worsened by the N-terminal Gly deletion, consistent with an increase in its helical content. Despite little impact on the antibacterial activity of G(IIKK)3I-NH2, deletion of both terminal amino acids greatly reduced its antitumor activity. Cholesterol present in tumor cell membrane-mimic was thought to constrain (IIKK)3-NH2 from penetrating into the cancerous membranes, evident from its lowest surface physical activity at penetrating model lipid membranes. On the other hand, its low toxicity to normal mammalian cells and high antibacterial activity in vitro and in vivo made it an attractive antibacterial agent. Thus, terminal modifications can help rebalance the different interactions involved and are highly effective at manipulating their selective membrane responses.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
1秒前
1秒前
CodeCraft应助潇洒的惋清采纳,获得10
1秒前
华仔应助bd采纳,获得10
1秒前
zz发布了新的文献求助100
2秒前
深情安青应助Niututu采纳,获得10
2秒前
cheng完成签到,获得积分10
3秒前
vulgar发布了新的文献求助30
4秒前
千秋完成签到,获得积分20
4秒前
大个应助lr采纳,获得10
4秒前
4秒前
知性的藏鸟完成签到 ,获得积分10
4秒前
传奇3应助lio采纳,获得10
4秒前
大模型应助小丁同学采纳,获得10
5秒前
酷波er应助cat采纳,获得10
5秒前
扑火飞蛾完成签到,获得积分10
6秒前
等风来完成签到,获得积分10
6秒前
白露完成签到 ,获得积分10
6秒前
7秒前
7秒前
cswcmrji发布了新的文献求助10
7秒前
sanshiqi完成签到,获得积分20
8秒前
超帅孱应助Irony采纳,获得20
9秒前
Jenna发布了新的文献求助10
9秒前
10秒前
Mason发布了新的文献求助20
10秒前
顾宗恒完成签到 ,获得积分10
10秒前
大模型应助ionize采纳,获得10
10秒前
在水一方应助毛日骏采纳,获得10
10秒前
科目三应助teqlt采纳,获得10
11秒前
兔子大王完成签到 ,获得积分10
11秒前
11秒前
rad1413发布了新的文献求助10
11秒前
科研通AI6.2应助peir采纳,获得10
11秒前
大个应助坦率曼梅采纳,获得10
11秒前
眼睛大的翠绿完成签到 ,获得积分10
12秒前
12秒前
13秒前
桐桐应助yz采纳,获得30
13秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
A Psychological Understanding of Criticism and Mental Health 600
Organizational Behavior 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7750549
求助须知:如何正确求助?哪些是违规求助? 9298174
关于积分的说明 20244548
捐赠科研通 7332468
什么是DOI,文献DOI怎么找? 3309630
关于科研通互助平台的介绍 2461212
邀请新用户注册赠送积分活动 2322183