Enhanced Delivery of Biomolecules into Caco2 Cells Based on the Cell-Penetrating Ability of Keratin Peptides

生物分子 生物物理学 生物相容性 角蛋白 细胞穿透肽 细胞粘附 细胞 共价键 材料科学 生物化学 化学 生物 有机化学 古生物学
作者
Xiaojie Qin,Yujie Guo,Ruilin Li,Johannes H. Bitter,Elinor L. Scott,Chunhui Zhang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (42): 56815-56825 被引量:3
标识
DOI:10.1021/acsami.4c13236
摘要

Keratin, as a promising bioresource, possesses significant potential for diverse biological applications due to its favorable biocompatibility, low toxicity, biodegradability, and cell adhesion ability. However, there are few studies on the cell-penetrating ability of keratin peptides (KEPs) for biomolecule delivery. Therefore, this study explored the cell-penetrating ability of KEPs with different molecular weights (Mw) on Caco2 cells using fluorescein-labeled insulin (FITC-INS) as the target intracellular biomolecule. The potential cell-penetrating mechanism was elaborated by combining cellular investigation with the physicochemical characterization of KEPs. The result shows that the KEPs <3 kDa (KEP1) exhibited the highest cell-penetrating ability at 2 mg/mL, allowing efficient delivery of FITC-INS into Caco2 cells without covalent bonding. The cellular uptake mechanism was energy-dependent, mainly involving macropinocytosis. The further fractionation of KEP1 reveals that the most effective components consisted of 8-19 amino acids, including specific hydrophobic peptides (e.g., RVVIEPSPVVV and IIIQPSPVVV), PPII amphipathic peptides (e.g., PPPVVVTFP and FIQPPPVVV), and Cys-rich peptides (e.g., LCAPTPCGPTPL and CLPCRPCGPTPL). Additionally, analysis of the secondary and tertiary structure and amino acid composition illustrated that KEP1 exhibited rich hydrophobic residues and disulfide bonds, which probably contributed to its cell-penetrating ability, as opposed to its small particle size and electrostatic interactions. This study reveals the cell-penetrating ability of KEPs, thus highlighting their potential as biomaterials for noncovalently delivering biomolecules.
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
老北京完成签到,获得积分10
刚刚
刚刚
孤星完成签到,获得积分10
刚刚
我是老大应助折耳根采纳,获得10
1秒前
古丁发布了新的文献求助10
1秒前
科研小白阳阳完成签到,获得积分10
1秒前
科研通AI6.4应助xiaoniuma采纳,获得10
1秒前
1秒前
yy发布了新的文献求助10
2秒前
Yanjiakun完成签到,获得积分10
2秒前
DDL完成签到,获得积分10
2秒前
2秒前
桐桐应助leslierui采纳,获得10
3秒前
努力考研完成签到 ,获得积分10
3秒前
风中的晓露完成签到 ,获得积分10
4秒前
村雨完成签到,获得积分10
4秒前
科研通AI6.4应助1703115采纳,获得10
4秒前
姜茂才完成签到,获得积分10
4秒前
4秒前
4秒前
纯真的冰蓝完成签到,获得积分10
4秒前
5秒前
5秒前
邱冯冯发布了新的文献求助10
6秒前
小林不熬夜完成签到,获得积分10
6秒前
淡然一德发布了新的文献求助10
6秒前
DW应助汤圆软软软采纳,获得10
6秒前
爆米花应助汤圆软软软采纳,获得10
6秒前
顾矜应助汤圆软软软采纳,获得10
6秒前
研友_VZG7GZ应助汤圆软软软采纳,获得10
7秒前
在水一方应助汤圆软软软采纳,获得10
7秒前
科研通AI6.2应助黄虹采纳,获得10
7秒前
搜集达人应助汤圆软软软采纳,获得10
7秒前
TE应助汤圆软软软采纳,获得10
7秒前
CipherSage应助汤圆软软软采纳,获得10
7秒前
orixero应助汤圆软软软采纳,获得10
7秒前
小绵完成签到,获得积分10
7秒前
修仙中应助汤圆软软软采纳,获得10
7秒前
ZHANG完成签到,获得积分10
7秒前
miko完成签到,获得积分10
7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
Nine new races of Peronospora manshurica found on soybeans in the Midwest 1000
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 600
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Eudora Welty and Modern Media 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7773002
求助须知:如何正确求助?哪些是违规求助? 9315146
关于积分的说明 20343439
捐赠科研通 7358673
什么是DOI,文献DOI怎么找? 3317118
关于科研通互助平台的介绍 2465619
邀请新用户注册赠送积分活动 2332235