Molecular Mechanism of P53 Peptide Permeation through Lipid Membranes from Solid-State NMR Spectroscopy and Molecular Dynamics Simulations

化学 分子动力学 渗透 核磁共振波谱 脂质双层 生物物理学 POPC公司 跨膜结构域 跨膜蛋白 膜生物学 计算化学 结晶学 立体化学 生物化学 生物 受体
作者
Mingyue Li,Jianguo Li,Xingyu Lu,Ryan Schroder,Arun Chandramohan,W. Peter Wuelfing,Allen C. Templeton,Wei Xu,Marian E. Gindy,Filippos Kesisoglou,Jing Ling,Tomi K. Sawyer,Chandra Verma,Anthony W. Partridge,Yongchao Su
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:146 (33): 23075-23091 被引量:1
标识
DOI:10.1021/jacs.4c04230
摘要

Macrocyclic peptides show promise in targeting high-value therapeutically relevant binding sites due to their high affinity and specificity. However, their clinical application is often hindered by low membrane permeability, which limits their effectiveness against intracellular targets. Previous studies focused on peptide conformations in various solvents, leaving a gap in understanding their interactions with and translocation through lipid bilayers. Addressing this, our study explores the membrane interactions of stapled peptides, a subclass of macrocyclic peptides, using solid-state nuclear magnetic resonance (ssNMR) spectroscopy and molecular dynamics (MD) simulations. We conducted ssNMR measurements on ATSP-7041M, a prototypical stapled peptide, to understand its interaction with lipid membranes, leading to an MD-informed model for peptide membrane permeation. Our findings reveal that ATSP-7041M adopts a stable α-helical structure upon membrane binding, facilitated by a cation-π interaction between its phenylalanine side chain and the lipid headgroup. This interaction makes the membrane-bound state energetically favorable, facilitating membrane affinity and insertion. The bound peptide displayed asymmetric insertion depths, with the C-terminus penetrating deeper (approximately 9 Å) than the N-terminus (approximately 4.3 Å) relative to the lipid headgroups. Contrary to expectations, peptide dynamics was not hindered by membrane binding and exhibited rapid motions similar to cell-penetrating peptides. These dynamic interactions and peptide-lipid affinity appear to be crucial for membrane permeation. MD simulations indicated a thermodynamically stable transmembrane conformation of ATSP-7041M, reducing the energy barrier for translocation. Our study offers an in silico view of ATSP-7041M's translocation from the extracellular to the intracellular region, highlighting the significance of peptide-lipid interactions and dynamics in enabling peptide transit through membranes.
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
澎鱼盐完成签到,获得积分10
刚刚
刚刚
平淡小丸子完成签到 ,获得积分10
刚刚
吃花生酱的猫完成签到,获得积分10
刚刚
1秒前
Vesper完成签到,获得积分10
1秒前
拼搏亦松发布了新的文献求助10
1秒前
无花果应助hu970采纳,获得10
2秒前
kk2024应助今天真暖采纳,获得20
2秒前
Brandy完成签到,获得积分10
2秒前
春景当思完成签到,获得积分10
2秒前
lyon发布了新的文献求助10
2秒前
3秒前
背后的广山完成签到,获得积分10
3秒前
Jiancui发布了新的文献求助10
3秒前
3秒前
3秒前
4秒前
体贴啤酒完成签到,获得积分10
4秒前
Ll发布了新的文献求助10
4秒前
5秒前
JOJO完成签到,获得积分10
5秒前
杭新晴完成签到 ,获得积分10
5秒前
淡然的日记本完成签到,获得积分10
5秒前
南方姑娘完成签到,获得积分10
6秒前
虚拟莫茗发布了新的文献求助20
6秒前
6秒前
7秒前
威武忆山完成签到 ,获得积分10
7秒前
凡而不庸举报有魅力发卡求助涉嫌违规
7秒前
壮观的访枫完成签到,获得积分10
7秒前
富婆嘉嘉子完成签到,获得积分10
7秒前
Healer完成签到 ,获得积分10
7秒前
羊羊发布了新的文献求助10
7秒前
JOJO发布了新的文献求助10
8秒前
9秒前
岁月轮回发布了新的文献求助10
9秒前
9秒前
送不送书7完成签到,获得积分10
9秒前
蘑菇发布了新的文献求助10
10秒前
高分求助中
Continuum Thermodynamics and Material Modelling 3000
Production Logging: Theoretical and Interpretive Elements 2700
Social media impact on athlete mental health: #RealityCheck 1020
Ensartinib (Ensacove) for Non-Small Cell Lung Cancer 1000
Unseen Mendieta: The Unpublished Works of Ana Mendieta 1000
Bacterial collagenases and their clinical applications 800
El viaje de una vida: Memorias de María Lecea 800
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 量子力学 光电子学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3527304
求助须知:如何正确求助?哪些是违规求助? 3107454
关于积分的说明 9285518
捐赠科研通 2805269
什么是DOI,文献DOI怎么找? 1539827
邀请新用户注册赠送积分活动 716708
科研通“疑难数据库(出版商)”最低求助积分说明 709672