thumbnail

Springer Science and Business Media LLC

SCIE-ISI SCOPUS (2009-2023)

  1865-5025

  1865-5033

 

Cơ quản chủ quản:  Springer New York , SPRINGER

Lĩnh vực:
Biochemistry, Genetics and Molecular Biology (miscellaneous)Modeling and Simulation

Các bài báo tiêu biểu

A Conversation on Artificial Intelligence, Chatbots, and Plagiarism in Higher Education
Tập 16 Số 1 - Trang 1-2 - 2023
Michael R. King
How to Measure Molecular Forces in Cells: A Guide to Evaluating Genetically-Encoded FRET-Based Tension Sensors
Tập 8 Số 1 - Trang 96-105 - 2015
Anna-Lena Cost, Pia Ringer, Anna Chrostek-Grashoff, Carsten Grashoff
Microtubule Tip Tracking and Tip Structures at the Nanometer Scale Using Digital Fluorescence Microscopy
Tập 4 Số 2 - Trang 192-204 - 2011
Alexei O. Demchouk, Melissa K. Gardner, David J. Odde
Mechanical Properties of the Tumor Stromal Microenvironment Probed In Vitro and Ex Vivo by In Situ-Calibrated Optical Trap-Based Active Microrheology
Tập 9 Số 3 - Trang 398-417 - 2016
Jack R. Staunton, Wilfred D. Vieira, King Leung Fung, Ross Lake, Alexus Devine, Kandice Tanner
Modification of Cellular Cholesterol Content Affects Traction Force, Adhesion and Cell Spreading
Tập 3 Số 2 - Trang 151-162 - 2010
Leann L. Norman, Ratna J. Oetama, Micah Dembo, Fitzroy J. Byfield, Daniel A. Hammer, Irena Levitan, Helim Aranda‐Espinoza
Effect of M1–M2 Polarization on the Motility and Traction Stresses of Primary Human Macrophages
Tập 9 Số 3 - Trang 455-465 - 2016
Laurel E. Hind, Emily Lurier, Micah Dembo, Kara L. Spiller, Daniel A. Hammer
Heparan Sulfate Regrowth Profiles Under Laminar Shear Flow Following Enzymatic Degradation
Tập 6 Số 2 - Trang 160-174 - 2013
Kristina Giantsos-Adams, Andrew Koo, Sukhyun Song, Jiro Sakai, Jagadish Sankaran, Jennifer Hyunjong Shin, Guillermo Garcı́a-Cardeña, C. Forbes Dewey
Co-Assembly Tags Based on Charge Complementarity (CATCH) for Installing Functional Protein Ligands into Supramolecular Biomaterials
Tập 9 - Trang 335-350 - 2016
Dillon T. Seroski, Antonietta Restuccia, Anthony D. Sorrentino, Kevin R. Knox, Stephen J. Hagen, Gregory A. Hudalla
Installing folded proteins into biomaterials is gaining interest for imparting functional properties that often cannot be provided by unfolded peptides or small molecules, such as catalysis, antigen conformation, or molecular recognition. Although covalent grafting provides a simple means to immobilize proteins onto pre-formed biomaterials, amenable chemistries can alter protein bioactivity, are relatively non-specific, and can be difficult to reproduce. Covalent fusions of bioactive molecules and synthetic peptides that can self-assemble into nano-scale architectures are a promising alternative for creating functional supramolecular biomaterials with precise and reproducible composition. Here we created a pair of oppositely charged synthetic peptides, referred to as “CATCH” (Co-Assembly Tags based on CHarge complementarity), to install folded proteins into supramolecular biomaterials. CATCH peptides co-assemble into β-sheet nanofibers when combined, yet cannot assemble independently due to electrostatic repulsion. Electrostatically controlled assembly enabled high yield production of soluble CATCH-green fluorescent protein (CATCH(−)GFP) by E. coli. Binary mixtures of CATCH-GFP and its charge-complementary peptide self-assembled into fluorescent microparticles, whereas ternary mixtures of CATCH(−)GFP and both CATCH peptides self-assembled into fluorescent nanofibers and macroscopic hydrogels. The CATCH system is therefore likely to be broadly useful for creating functional supramolecular biomaterials with integrated folded protein components for various biomedical and biotechnological applications.