Zobrazeno 1 - 10
of 14
pro vyhledávání: '"J David Pajerowski"'
Autor:
James M Wagner, J David Pajerowski, Christopher L Daniels, Patrick M McHugh, Jessica A Flynn, John W Balliet, Danilo R Casimiro, Shyamsundar Subramanian
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94401 (2014)
Chikungunya virus-like particles (VLPs) have potential to be used as a prophylactic vaccine based on testing in multiple animal models and are currently being evaluated for human use in a Phase I clinical trial. The current method for producing these
Externí odkaz:
https://doaj.org/article/de84d5cc23ff4b7a97129b9a9cf8fabb
Autor:
Dennis E. Discher, Karthikan Rajagopal, Abdullah Mahmud, Sharon M. Loverde, André Ex Brown, J. David Pajerowski, David A. Christian
Publikováno v:
Macromolecules. 43:9736-9746
Crystallization processes are in general sensitive to detailed conditions, but our present understanding of underlying mechanisms is insufficient. A crystallizable chain within a diblock copolymer assembly is expected to couple curvature to crystalli
Autor:
J. David Pajerowski, Diana M. Bowen, Younghoon Kim, David A. Christian, Shenshen Cai, Dennis E. Discher
Publikováno v:
European Journal of Pharmaceutics and Biopharmaceutics. 71:463-474
Polymersomes are polymer-based vesicular shells that form upon hydration of amphiphilic block copolymers. These high molecular weight amphiphiles impart physicochemical properties that allow polymersomes to stably encapsulate or integrate a broad ran
Autor:
Younghoon, Kim, Manorama, Tewari, J David, Pajerowski, Shenshen, Cai, Shamik, Sen, Jason H, Williams, Jason, Williams, Shashank R, Sirsi, Shashank, Sirsi, Gordon J, Lutz, Gordon, Lutz, Dennis E, Discher
Publikováno v:
Journal of Controlled Release. 134:132-140
siRNA and antisense oligonucleotides, AON, have similar size and negative charge and are often packaged for in vitro delivery with cationic lipids or polymers-but exposed positive charge is problematic in vivo. Here we demonstrate loading and functio
Publikováno v:
Proceedings of the National Academy of Sciences. 104:15619-15624
Cell differentiation in embryogenesis involves extensive changes in gene expression structural reorganization within the nucleus, including chromatin condensation and nucleoprotein immobilization. We hypothesized that nuclei in naive stem cells would
Publikováno v:
Biophysical Journal. 89:2855-2864
Force-induced changes in genome expression as well as remodeling of nuclear architecture in development and disease motivate a deeper understanding of nuclear mechanics. Chromatin and green fluorescent protein-lamin B dynamics were visualized in a mi
Autor:
Amnon Buxboim, J. David Pajerowski, David W. Speicher, Joel Pinter, Joe Swift, Manorama Tewari, Florian Rehfeldt, Dennis E. Discher, P.C. Dave P. Dingal, Irena L. Ivanovska, Takamasa Harada, Kyle R. Spinler, Jae-Won Shin
Publikováno v:
Science (New York, N.Y.). 341(6149)
Label-free quantitation and characterization of proteins by mass spectrometry (MS) is now feasible, especially for moderately expressed structural proteins such as lamins that typically yield dozens of tryptic peptides from tissue cells. Using standa
Publikováno v:
Methods in cell biology. 98
The genome is virtually identical in all cells within an organism, with epigenetic changes contributing largely to the plasticity in gene expression during both development and aging. These changes include covalent modifications of chromatin componen
Autor:
J. David Pajerowski, David W. Speicher, Brian C. Chase, Dennis E. Discher, Hsin-Yao Tang, Diego A. Pantano
Publikováno v:
Biophysical Journal. 100:371a
Protein unfolding, disassembly, and aggregation underlie many diseases, but detailed study of these processes in intact cells has been limited. Cysteine Shotgun labeling utilizes cell-permeable fluorescent dyes to label exposed cysteine residues and
Autor:
David W. Speicher, J. David Pajerowski, Joe Swift, Brian C. Chase, Hsin-Yao Tang, Diego A. Pantano, Dennis E. Discher
Publikováno v:
Biophysical Journal. 98:447a
The study of protein folding and stability is typically conducted with purified proteins by methods that are exacting but lack the ability to analyze complex mixtures of proteins. To study proteins in their native environments inside a cell or isolat