Visvanathan Ramamurthy, PhD
PO Box 9193
E230 WVU Eye Institute & 3126 HSC-N
1 Medical Center Drive
Morgantown, WV 26506
Protein trafficking in neurons
Proteins move at the rate of 1000 molecules per second in photoreceptor cells between different compartments. Defects in this process lead to blindness in humans. How do proteins move at this rapid rate? How are proteins retained in different compartments? We are currently testing our hypothesis that small GTPases play an important role in regulating protein trafficking between different regions of photoreceptor cells.
Protein assembly and function
How do multimeric proteins assemble? We use phosphodiesterase-6 as a model system to understand protein assembly. We believe protein-lipid modification contributes to this process and are currently testing this hypothesis.
Treatment(s) for neurodegenerative diseases
We used adeno-associated viral mediated gene therapy to restore vision in a mouse model for severe childhood blindness. We hope to expand this line of research using cutting-edge genome engineering methods such as TALENs and CRISPR system for stem cell therapy.
Small molecules, translational suppressors, treatment for blindness?
As an alternative to gene therapy, we are exploring the use of small molecule translational read-through suppressors to overcome non-sense mutations that lead to diseases. This project is in collaboration with Dr. Brian Popp in the Chemistry Department.
Splicing and blinding diseases
Defects in ubiquitously expressed splicing genes are a cause of retinitis pigmentosa (RP) in humans. In collaboration with Dr. Peter Stoilov at Biochemistry, we are identifying the mechanism behind splicing defects and blindness. The hope is to use the knowledge gained in this study to design novel treatments for patients with RP.
Grants and Research
NIH R01 (2007-2016)
- Dilan TL, Singh RK, Saravanan T, MOye A, Goldberg AFX, Stoilov P,Ramamurthy V (2017). Bardet–Biedl syndrome-8 (BBS8) protein is crucial for the development of outer segments in photoreceptor neurons. Hum Mol Genet, 27(2):283-294.
- Murphy D, Cieply B, Carstens R, Ramamurthy V, Stoilov P (2016). The Musashi 1 controls the splicing of photoreceptor-specific exons in the vertebrate retina. PLoS Genet, 12(8):e1006256. PMCID: PMC4991804
- Christiansen JR, Pendse ND, Kolandaivelu S, Bergo MO, Young SG, Ramamurthy V (2016). Deficiency of Isoprenylcysteine Carboxyl Methyltransferase (ICMT) leads to progressive loss of photoreceptor function. J Neurosci, 36(18):5107-14. PMCID: PMC4854971
- Murphy D, Kolandaivelu S, Ramamurthy V, Stoilov P (2016). Analysis of alternative pre-RNA splicing in the mouse retina using a fluorescent reporter. Methods Mol Biol, 1421:269-86.
- Wright ZC, Singh RK, Alpino R, Goldberg AF, Sokolov M, Ramamurthy V(2016). ARL3 regulates trafficking of prenylated phototransduction proteins to the rod outer segment. Hum Mol Genet, 25(10):2031-2044. PMCID: PMC5062590
- Murphy D, Singh R, Kolandaively S, Ramamurthy V, Stoilov P (2015). Alternative splicing shapes the phenotype of a mutation in BBS8 to cause nonsyndromic retinitis pigmentosa. Mol Cell Biol, 35(10):4860-70. PMCID: PMC4405636
- Singh RK, Kolandaivelu S, Ramamurthy V (2014). Early alteration of retinal neurons in Aipl1-/- animals. Invest Ophthalmol Vis Sci, 55(5):3081-92. PMCID: PMC4034756
- Kolandaivelu S, Ramamurthy V (2014). AIPL1 protein and its indispensable role in cone photoreceptor function and survival. Adv Exp Med Biol, 801:43-8.
- Kolandaivelu S, Singh RK, Ramamurthy V (2014). AIPL1, A protein linked to blindness, is essential for the stability of enzymes mediating cGMP metabolism in cone photoreceptor cells. Hum Mol Genet, 23(4):1002-12. PMCID: PMC3900108
- Christiansen JR, Ramamurthy V (2012). Greasing the protein trafficking machinery of photoreceptor neurons: role for post prenylation processing of proteins. Cell Logist, (2(1):15-19. PMCID: PMC3355970
- Christiansen JR, Kolandaivelu S, Bergo MO, Ramamurthy V (2011). RAS-converting enzyme 1-mediated endoproteolysis is required for trafficking of rod phosphodiesterase 6 to photoreceptor outer segments. Proc Natl Acad Sci U S A, 108(21):8862-6. PMCID: PMC3102416
- Kolandaivelu S, Chang B, Ramamurthy V (2011). Rod Phosphodiesterase-6 (PDE6) catalytic subunits restores cone function in a mouse model lacking cone PDE6 catalytic subunit. J Biol Chem, 286(38):33252-9. PMCID: PMC3190866
- Ku C*, Chiodo V, Boye S, Goldberg A, Li T, Hauswirth W, Ramamurthy V(2011). Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosis. Hum Mol Genet, 20(23):4569-81. PMCID: PMC3209828
- Kirschman LT, Kolandaivelu S, Frederick JM, Dang L, Goldberg AF, Baehr W,Ramamurthy V (2010) . The Leber congenital amaurosis protein, AIPL1, is needed for the viability and functioning of cone photoreceptor cells. Hum Mol Genet, 19(6):1076-87. PMCID: PMC2830831