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Cell surface functionalization has emerged as a powerful strategy for modulating cellular behavior and expanding cellular capabilities beyond their intrinsic biological limits. Natural phenolic molecules present as 'green' and versatile building blocks for constructing cell-based biomanufacturing and biotherapeutic platforms. Due to the abundant catechol or galloyl groups, phenolic molecules can dynamically and reversibly bind to versatile substrates multiple molecular interactions. A range of self-assembled cytoadhesive polyphenol-functionalized nanoarchitectures (cytoPNAs) can be formed metal coordination or macromolecular self-assembly that can rapidly attach to cell surfaces in a cell-agnostic manner. Additionally, the cytoPNAs attached on the cell surface can also provide active sites for the conjunction of bioactive payloads, further expanding the structural repertoire and properties of engineered cells. This Perspective introduces the wide potential of cytoPNA-mediated cell engineering in three key applications: (1) creating inorganic-organic biohybrids as cell factories for efficient production of high-value chemicals, (2) constructing engineered cells for cell-based therapies with enhanced targeting specificity and nano-bio interactions, and (3) encapsulating microbes as biotherapeutics for the treatment of gastrointestinal tract-related diseases. Collectively, the rapid, versatile, and modular nature of cytoPNAs presents a promising platform for next-generation cell engineering and beyond.
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http://dx.doi.org/10.1039/d4sc07198k | DOI Listing |
ACS Biomater Sci Eng
September 2025
Materials Engineering, McGill university, Montreal H3A0C5, Canada.
Transcutaneous devices such as dental implants frequently fail due to infections at their interfaces with epithelial tissues. These infections are facilitated by the lack of integration between the devices and the surrounding soft tissues. This study aims to improve epithelial integration through surface modification of a transcutaneous implant material (polyetheretherketone (PEEK)).
View Article and Find Full Text PDFPLoS Genet
September 2025
Department of Biology/Chemistry, Division of Genetics, University of Osnabrück, Barbarastrasse, Osnabrück, Germany.
The small GTPase Rho5 has been shown to be involved in regulating the Baker's yeast response to stress on the cell wall, high medium osmolarity, and reactive oxygen species. These stress conditions trigger a rapid translocation of Rho5 and its dimeric GDP/GTP exchange factor (GEF) to the mitochondrial surface, which was also observed upon glucose starvation. We here show that rho5 deletions affect carbohydrate metabolism both at the transcriptomic and the proteomic level, in addition to cell wall and mitochondrial composition.
View Article and Find Full Text PDFDermatology
September 2025
Department of Clinical Pharmacology and Toxicology, University of Geneva, Geneva, Switzerland.
Background: Maintaining homeostasis in the upper pilosebaceous unit in acne-prone skin has emerged as the primary goal for effective and long-term acne management.
Summary: In this review, we describe advances in acne research that have helped redefine the strategic targets for new topical acne treatments, providing the basis for new therapeutic strategies that may allow this goal to be achieved.
Key Messages: First, we describe the results of studies analyzing apparently uninvolved skin from individuals with acne, using sequential skin surface biopsies.
Clin Cancer Res
September 2025
University of Washington and Fred Hutchinson Cancer Research Center, Seattle, WA, United States.
Human Kallikrein 2 (KLK2) is a prostate cancer tissue specific protein that is regulated by androgen receptor (AR) signaling. KLK2 was not previously recognized as a therapeutic target as it is secreted. It has now been demonstrated that KLK2 is expressed on the cell surface and targetable by various methodologies.
View Article and Find Full Text PDFProbiotics Antimicrob Proteins
September 2025
School of Life Science, Liaoning Normal University, Dalian, 116081, China.
Cutibacterium acnes (C. acnes, formerly classified as Propionibacterium acnes) is a Gram-positive bacterium that contributes to the development of acne vulgaris, resulting in inflammation and pustule formation on the skin. In this study, we developed and synthesized a series of antimicrobial peptides (AMPs) that are derived from the skin secretion of Rana chensinensis.
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