Yong‐beom Lim
Yonsei University · 材料科学
研究室紹介
Professor Yong-beom Lim's research lab specializes in the design and development of advanced biodegradable polymers and nanostructured materials for biomedical applications, particularly in gene delivery and regenerative medicine. The lab focuses on creating smart, multifunctional polymeric systems that combine controlled degradation, biocompatibility, and efficient nucleic acid delivery through rational molecular engineering. Key research directions include the synthesis of biodegradable polycations, hyperbranched polymers, and supramolecular nanostructures that enable safe and effective gene transfection with minimal cytotoxicity. The lab also explores non-covalent assembly strategies using host-guest interactions for the construction of stimuli-responsive nanocarriers.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15Supramolecular nanostructures covered with bioactive functional molecules have been actively explored as promising materials in the field of biotechnology. Recent advances in nano-sized chemistry have made it possible to fabricate various kinds of nanostructures with tailor-made nanostructural properties. This, combined with appropriate bioactive functionalization, has led to the successful utilization of supramolecular nanostructures in diverse biomaterials applications. This tutorial review de
The success of gene therapy is largely dependent on the delivery vector system. Efficient transfection and nontoxicity are two of the most important requirements of an ideal gene delivery vector. To generate both an efficient and nontoxic vector, we rationally constructed polymeric vectors to have simultaneous multiple functions, i.e., controlled degradation, an endosome disruptive function, and positive charges. Remarkably, the transfection efficiency of network poly(amino ester) (n-PAE) synthe
A self-destroying, biodegradable, and polycationic polyester, poly( trans -4-hydroxy- l -proline ester) (PHP ester), was synthesized, and the interaction of the polymer with polyanion DNA was investigated. Degradation of the polymer in aqueous solution was investigated by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) and by measuring the pH change as carboxylic acids are formed as products of the degradation of the polymer backbone ester bond. It was
ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTDevelopment of a Safe Gene Delivery System Using Biodegradable Polymer, Poly[α-(4-aminobutyl)-l-glycolic acid]Yong-beom Lim, Chang-hwan Kim, Kwan Kim, Sung Wan Kim, and Jong-sang ParkView Author Information School of Chemistry & Molecular Engineering Seoul National University, Seoul 151-742, Korea Center for Controlled Chemical Delivery (CCCD) University of Utah, Salt Lake City, Utah 84112 Cite this: J. Am. Chem. Soc. 2000, 122, 27, 6524–6525Publ
ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTCationic Hyperbranched Poly(amino ester): A Novel Class of DNA Condensing Molecule with Cationic Surface, Biodegradable Three-Dimensional Structure, and Tertiary Amine Groups in the InteriorYong-beom Lim, Seon-Mi Kim, Yan Lee, Woo-kyoung Lee, Tae-gyun Yang, Min-jae Lee, Hearan Suh, and Jong-sang ParkView Author Information School of Chemistry & Molecular Engineering Seoul National University, Seoul 151-742, Korea Cite this: J. Am. Chem. Soc. 2001
A ternary complex of PPI-DAB dendrimer [(1,4-diaminobutane); Gen = N; dendri-poly(propyleneimine); -[NHC(=O)CH(2)NH(2)(+)(CH(2))(4)NH(3)(+)](z)()], DNA, and cucurbituril (CB) was evaluated as an example of a totally self-assembled gene delivery carrier. The complex was formed in a noncovalent way in which DNA interacts with PPI-DAB electrostatistically and CB with PPI-DAB through multiple noncovalent interactions. Dynamic light scattering data indicated that the diameter and size distributions o
Past decades have witnessed rapidly growing interest in nanometer-sized structures, which have great potential to be used in a variety of applications, such as electronics, sensors, coatings, and biomaterials. Supramolecular chemistry in particular has been actively applied to the development of such materials. Nanostructures can readily be accessed using bottom-up supramolecular approaches as they are composed of small molecules (supramolecular building blocks) requiring fewer steps to synthesi
Wrap it up: Nanoribbons coated with cell-penetrating peptides (CPPs) allowed the encapsulation of hydrophobic guest molecules. The nanoassembly internalized into mammalian cells with high efficiency and showed selective intracellular compartmentalization owing to its sensitivity to the solution environment.
Therapeutic viruses: A filament-shaped artificial virus is formed by using a preorganized supramolecular nanoribbon as a template. The artificial virus (see picture), which is composed of the nanoribbon, small interfering RNAs (blue, double-helix shape), and hydrophobic guests (red), is highly efficient in delivering genes and drugs to the inside of cells.
Protein roll call: Peptide-based building blocks, in which both an alpha-helix-forming segment and a beta-sheet segment are located within a single macrocyclic structure, self-assemble into alpha-helix-decorated artificial proteins. This approach provides a starting point for developing artificial proteins that can modulate alpha-helix-mediated interactions occurring in a multivalent fashion.
We demonstrate here the rational design strategy to control the length of 1-dimensional beta-sheet peptide nanoassembly. We synthesized the beta-sheet peptides with attached coils and carbohydrates. We reasoned that the bulkiness of the coils affects the final length of the assembled beta-sheet peptide nanostructures because of the steric crowding effect. The nanostructure from the peptide with a small and linear coil was several micrometers long, whereas the one from the peptide with a high-vol
Here we ask the fundamental questions about the effect of peptide topology on self-assembly. The study revealed that the self-assembling behaviors of cyclic and linear peptides are significantly different in several respects, in addition to sharing several similarities. Their clear differences included the morphological dissimilarities of the self-assembled nanostructures and their thermal stability. The similarities include their analogous critical aggregation concentration values and cytotoxic