Research Bio
Dr. Peng's research interests are multifunctional extracellular matrix protein hensin, which plays an important role in adaptation of intercalated cells during metabolic acidosis. Hensin have also been associated with epithelial differentiation, and tumor suppression. Although hensin was founded ten years ago, full-length hensin cloning and expression is still not available. So far, hensin can only be obtained from natural source such as , cell medium, cell lysates, etc. Recombinant expression and purification of hensin is an essential and key step for systematic investigating its structure, function, signal transduction pathway and towards the evaluation of its therapeutically potential.
Dr. Peng's some research aims are as follows:
1) Cloning, sequencing, and expression full-lenth hensin gene as well as its different domains, such as SRCR, Zp, and CUB domain.
2) Structural and functional analysis of hensin. Investigating the mechanisms of hensin polymerizing in ECM and determining other proteins interacting with hensin such as cyclophilins, galectin-3, integrins and so on.
3) Investigating hensin signaling pathway.
2013
Soundarapandian, V.; Peng, H.; Schwartz , GJ. "Galectin-3 mediates oligomerization of secreted hensin using its carbohydrate-recognition domain." American Journal of Physiology - Renal Physiology. 2013 Jul 1;305 (1):F90-9." Am J Physiol Renal Physiol. 2013; 305: F90-F99. |
2009
Peng H, Soundarapandian V, Schiene-Fischer C, Li Hui, Purkerson JM, Malesevic, M, Liebscher J, Al-Awqati Q, Schwartz GJ. "Secreted Cyclophilin A, a Peptidylprolyl cis-trans Isomerase, mediates Matrix Assembly of Hensin, a Protein Implicated in Epithelial Differentiation." Journal of Biological Chemistry. 2009; 284(10): 6465-6475. |
2006 Jan 1
Sahni A, Khorana AA, Baggs RB, Peng H, Francis CW. "FGF-2 binding to fibrin(ogen) is required for augmented angiogenesis." Blood. 2006 Jan 1; 107(1):126-31. Epub 2005 Sep 13. |
2004 Mar 15
Peng H, Sahni A, Fay P, Bellum S, Prudovsky I, Maciag T, Francis CW. "Identification of a binding site on human FGF-2 for fibrinogen." Blood. 2004 Mar 15; 103(6):2114-20. Epub 2003 Nov 20. |
2002 May
Peng H, Myers J, Fang X, Stachowiak EK, Maher PA, Martins GG, Popescu G, Berezney R, Stachowiak MK. "Integrative nuclear FGFR1 signaling (INFS) pathway mediates activation of the tyrosine hydroxylase gene by angiotensin II, depolarization and protein kinase C." Journal of neurochemistry. 2002 May; 81(3):506-24. |
