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QMU

Advancing animal-free organ-on-a-chip with PeptiMatrix

Queen Mary University of London School of Engineering and Materials Science
✓ Fully Funded 🎓 Bioengineering 🎓 Biomedical Engineering 🎓 Materials Science organ-on-a-chip peptimatrix synthetic hydrogels musculoskeletal tissue 3d cell culture extracellular matrix mechanobiology

Explore synthetic peptide hydrogels to replace animal-derived ECM in organ-on-a-chip models. Test PeptiMatrix formulations for musculoskeletal tissue engineering across leading OoC platforms. Innovate animal-free 3D microenvironments with wide impact potential.

AI-generated overview

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Why This Research Matters

This project addresses critical limitations of current organ-on-a-chip models by eliminating animal-derived ECM components, reducing animal use in research. Developing synthetic, customizable hydrogels with suitable mechanical and biochemical properties will enhance model reproducibility and physiological relevance, accelerating drug discovery and musculoskeletal disease research.

primary cilia cartilage bioengineering mechanobiology organ-on-a-chip

Project Description

Project Overview

The extracellular matrix (ECM) is a three-dimensional (3D), bioactive, instructive network that regulates cell behaviour through biochemical and biophysical cues. The ECM plays a crucial role in musculoskeletal (MSK) tissue development, function and dysfunction and should be considered an essential component in the design of Organ-on-a-Chip (OoC) models.

Paradoxically, given the animal replacement potential of OoC, many hydrogels currently used to mimic the 3D ECM in MSK OoC systems are animal-derived, e.g. Matrigel™ and type 1 collagen. These represent a significant, overlooked source of animal use that requires replacement. Furthermore, animal-derived hydrogels are ill-defined, poorly customizable, vary between batches, and lack sufficient mechanical properties.

This project addresses this gap by using PeptiMatrix™, a fully synthetic and customizable peptide hydrogel platform designed for 3D cell culture. PeptiMatrix™ exists in different stiffness formulations and functional augmentations.

What You Will Do

The PhD will evaluate PeptiMatrix™ formulations for use in multiple OoC platforms (Emulate, MIMETAS, BiomimX), modeling various MSK tissues such as synovium, cartilage, and bone. Key assessments will include the gels’ ability to maintain MSK cell viability and phenotype, transmit mechanical strain, and generate physiologically relevant engineered MSK tissues within the OoC environment. Collaboration with the PeptiMatrix™ team will provide technical and strategic consultancy.

Expected Outcomes

The project aims to redefine 3D tissue microenvironments in MSK organ-on-a-chip systems and develop animal-free, well-characterized hydrogel materials with improved mechanical and biochemical properties. The outcomes could extend beyond MSK tissues, impacting the broader field of organ-on-a-chip technology.

Why This Matters

Developing animal-free hydrogels will reduce animal use in research, enhance reproducibility and customization of OoC models, and enable more physiologically relevant tissue engineering approaches. This aligns with ethical goals and technical needs for next-generation organ-on-a-chip systems essential for drug discovery, disease modeling, and regenerative medicine.

Entry Requirements

Enthusiasm for organ-on-a-chip technologies with backgrounds such as biology, biochemistry, genetics, materials science, biomedical engineering or related fields. Some experimental laboratory experience and motivation to develop relevant skills are expected. Specific prior experience is not required as training will be provided.

How to Apply

Applications are through the COaCT admissions process. Candidates should apply once to COaCT and list project preferences at http://www.cpm.qmul.ac.uk/cdt/projects/projects2026open. Further application details are available at http://www.cpm.qmul.ac.uk/cdt/applications/stepbystep.

Eligibility

UK/Home
EU
International

Supervisor Profile

PM
Prof Martin Knight
Queen Mary University of London, School of Engineering and Materials Science
8190 Citations
55 h-index
Google Scholar

Prof Martin Knight is a leading mechanobiologist at Queen Mary University of London, focusing on primary cilia, cartilage biology, and organ-on-a-chip technology. His research involves understanding mechanotransduction in musculoskeletal tissues and developing bioengineered models that mimic physiological tissue mechanics. He is internationally recognized in the field with a strong publication record exceeding 8000 citations and an h-index over 50.

Key Publications

2018 371 citations
Deconstruction of a metastatic tumor microenvironment reveals a common matrix response in human cancers
2012 263 citations
Primary cilia mediate mechanotransduction through control of ATP-induced Ca2+ signaling in compressed chondrocytes
2000 211 citations
Beta transition and stress-induced phase separation in the spinning of spider dragline silk
2000 190 citations
Chondrocyte deformation within compressed agarose constructs at the cellular and sub-cellular levels
2001 183 citations
Mechanical compression influences intracellular Ca2+ signaling in chondrocytes seeded in agarose constructs

Research Contributions

Elucidation of the role of primary cilia in mechanotransduction and signaling in chondrocytes under mechanical compression.
Provided insights that advance understanding of cellular mechanobiology and potential targets for cartilage-related disease treatments.
Characterization of cellular and sub-cellular deformation of chondrocytes within agarose constructs under mechanical compression.
Enhanced biomechanical knowledge useful for tissue engineering and regenerative medicine strategies.
Investigation of stress-induced phase behavior in spider dragline silk spinning.
Contributed to biomaterials research with implications for designing synthetic silk and related materials.

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