Nanofibrous Peptide Hydrogels Leveraging Histidine to Modulate pH-Responsive Supramolecular Assembly and Antibody Release

被引:0
|
作者
Saenz, Gabriel [1 ]
Pogostin, Brett H. [2 ]
Cole, Carson C. [1 ]
Agrawal, Anushka [2 ]
Chew-Martinez, Danielle [1 ]
Dubackic, Marija [3 ]
Pal, Antara [4 ,5 ]
Olsson, Ulf [3 ]
Mchugh, Kevin J. [1 ,2 ]
Hartgerink, Jeffrey D. [1 ,2 ]
机构
[1] Rice Univ, Dept Chem, Houston, TX 77005 USA
[2] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[3] Lund Univ, Div Phys Chem, SE-22100 Lund, Sweden
[4] Stockholm Univ, Dept Phys, SE-22100 Stockholm, Sweden
[5] MAX IV Lab, SE-22100 Lund, Sweden
基金
瑞典研究理事会;
关键词
MULTIDOMAIN PEPTIDES; DRUG-DELIVERY; PROGRESSION; PREVENTS; DESIGN;
D O I
10.1021/acs.biomac.4c01296
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this work, we investigate the pH-responsive behavior of multidomain peptide (MDP) hydrogels containing histidine. Small-angle X-ray scattering confirmed that MDP nanofibers sequester nonpolar residues into a hydrophobic core surrounded by a shell of hydrophilic residues. MDPs with histidine on the hydrophilic face formed nanofibers at all pH values tested, but the morphology of the fibers was influenced by the protonation state and the location of histidine in the MDP sequence. MDPs with histidine residues within the hydrophobic face disassemble below physiological pH and form nanofibers at higher pH. Taking advantage of their stimulus-triggered behavior, an anti-PD-1 antibody was loaded into histidine MDP hydrogels to examine pH-dependent differences in payload delivery in vitro. Hydrogels composed of MDPs with histidine on the hydrophilic face demonstrated pH-dependent payload retention. Additionally, they showed significantly slower antibody release and reduced antibody diffusion rates in vitro compared to MDP hydrogels lacking histidine.
引用
收藏
页数:13
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