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1.
Biomacromolecules ; 25(1): 258-271, 2024 01 08.
Artigo em Inglês | MEDLINE | ID: mdl-38110299

RESUMO

Protein hydrogels represent an important and growing biomaterial for a multitude of applications, including diagnostics and drug delivery. We have previously explored the ability to engineer the thermoresponsive supramolecular assembly of coiled-coil proteins into hydrogels with varying gelation properties, where we have defined important parameters in the coiled-coil hydrogel design. Using Rosetta energy scores and Poisson-Boltzmann electrostatic energies, we iterate a computational design strategy to predict the gelation of coiled-coil proteins while simultaneously exploring five new coiled-coil protein hydrogel sequences. Provided this library, we explore the impact of in silico energies on structure and gelation kinetics, where we also reveal a range of blue autofluorescence that enables hydrogel disassembly and recovery. As a result of this library, we identify the new coiled-coil hydrogel sequence, Q5, capable of gelation within 24 h at 4 °C, a more than 2-fold increase over that of our previous iteration Q2. The fast gelation time of Q5 enables the assessment of structural transition in real time using small-angle X-ray scattering (SAXS) that is correlated to coarse-grained and atomistic molecular dynamics simulations revealing the supramolecular assembling behavior of coiled-coils toward nanofiber assembly and gelation. This work represents the first system of hydrogels with predictable self-assembly, autofluorescent capability, and a molecular model of coiled-coil fiber formation.


Assuntos
Simulação de Dinâmica Molecular , Proteínas , Espalhamento a Baixo Ângulo , Difração de Raios X , Proteínas/química , Hidrogéis
3.
ACS Biomater Sci Eng ; 10(5): 3425-3437, 2024 05 13.
Artigo em Inglês | MEDLINE | ID: mdl-38622760

RESUMO

Triple-negative breast cancer (TNBC) lacks expressed protein targets, making therapy development challenging. Hydrogels offer a promising new route in this regard by improving the chemotherapeutic efficacy through increased solubility and sustained release. Moreover, subcutaneous hydrogel administration reduces patient burden by requiring less therapy and shorter treatment times. We recently established the design principles for the supramolecular assembly of single-domain coiled-coils into hydrogels. Using a modified computational design algorithm, we designed Q8, a hydrogel with rapid assembly for faster therapeutic hydrogel preparation. Q8 encapsulates and releases doxorubicin (Dox), enabling localized sustained release via subcutaneous injection. Remarkably, a single subcutaneous injection of Dox-laden Q8 (Q8•Dox) significantly suppresses tumors within just 1 week. This work showcases the bottom-up engineering of a fully protein-based drug delivery vehicle for improved TBNC treatment via noninvasive localized therapy.


Assuntos
Preparações de Ação Retardada , Doxorrubicina , Hidrogéis , Neoplasias de Mama Triplo Negativas , Doxorrubicina/farmacologia , Doxorrubicina/administração & dosagem , Doxorrubicina/química , Doxorrubicina/uso terapêutico , Hidrogéis/química , Neoplasias de Mama Triplo Negativas/tratamento farmacológico , Neoplasias de Mama Triplo Negativas/patologia , Feminino , Humanos , Animais , Preparações de Ação Retardada/química , Linhagem Celular Tumoral , Engenharia de Proteínas , Camundongos , Liberação Controlada de Fármacos , Antibióticos Antineoplásicos/administração & dosagem , Antibióticos Antineoplásicos/farmacologia , Antibióticos Antineoplásicos/uso terapêutico , Antibióticos Antineoplásicos/química
4.
Biomater Sci ; 12(11): 2951-2959, 2024 May 28.
Artigo em Inglês | MEDLINE | ID: mdl-38656316

RESUMO

The development of targeted anti-cancer therapeutics offers the potential for increased efficacy of drugs and diagnostics. Utilizing modalities agnostic to tumor type, such as the hypoxic tumor microenvironment (TME), may assist in the development of universal tumor targeting agents. The hypoxia-inducible factor (HIF), in particular HIF1, plays a key role in tumor adaptation to hypoxia, and inhibiting its interaction with p300 has been shown to provide therapeutic potential. Using a multivalent assembled protein (MAP) approach based on the self-assembly of the cartilage oligomeric matrix protein coiled-coil (COMPcc) domain fused to the critical residues of the C-terminal transactivation domain (C-TAD) of the α subunit of HIF1 (HIF1α), we generate HIF1α-MAP (H-MAP). The resulting H-MAP demonstrates picomolar binding affinity to p300, the ability to downregulate hypoxia-inducible genes, and in vivo tumor targeting capability.


Assuntos
Subunidade alfa do Fator 1 Induzível por Hipóxia , Engenharia de Proteínas , Subunidade alfa do Fator 1 Induzível por Hipóxia/metabolismo , Subunidade alfa do Fator 1 Induzível por Hipóxia/química , Humanos , Animais , Domínios Proteicos , Camundongos , Linhagem Celular Tumoral , Proteína de Matriz Oligomérica de Cartilagem/química , Proteína de Matriz Oligomérica de Cartilagem/metabolismo , Microambiente Tumoral , Proteína p300 Associada a E1A/metabolismo , Proteína p300 Associada a E1A/química
5.
Rev Sci Instrum ; 94(4)2023 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-38081265

RESUMO

The balanced field electromagnetic technique is an effective way of in-line inspection to detect cracks in pipelines. A signal demodulation method based on phase characteristics is proposed for the problem of interference signals generated by the sensor tilt shaking during the detection, which affects the judgment of the cracks. The method uses a reference signal whose phase is orthogonal to the signal generated by the sensor shaking to demodulate the detection signal to eliminate the shake interference. The generation principles of crack detection signals and interference signals generated by sensor shaking are analyzed, and the influence of sensor lift-off on detection is compared. A demodulation model is established based on the characteristic of that same frequency and different phases of crack and shake signals. The feasible conditions of the method are analyzed by simulation, and the phase value of the reference signal in the demodulation method is determined. The platform detection experiment and pulling tests at different speeds are carried out, respectively, to verify the effectiveness of the proposed method. The results show that there is a significant phase difference between the signals generated by the sensor shaking and the crack. For carbon steel pipelines, the signal phase of different shake angles is -4°. When the sensor structure and excitation frequency in this study are used, the reference signal phase is chosen to be 86°. The method preserves the detection signal characteristics before processing and enables the linear output responses to be obtained for different depths of cracks.

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