Manojkumar A. Puthenveedu-Department of Biological Sciences - Carnegie Mellon University

Manojkumar A. Puthenveedu

Assistant Professor

Address:
202 Mellon Institute
Department of Biological Sciences
Carnegie Mellon University
4400 Fifth Avenue
Pittsburgh, PA 15213
Phone: 412-268-8236
Fax: 412-268-7129

Education

M.B.,B.S., Calicut Medical College, India
Ph.D., Carnegie Mellon
Postdoctoral Appointment, University of California, San Francisco

Research

How does membrane trafficking control and co-ordinate the complex signaling pathways in the brain? Normal signaling depends on accurate localization of signaling receptors in specific regions of the cell, and trafficking plays a critical role in controlling this localization. Despite this obvious significance, we still know very little about the protein machineries that mediate trafficking of signaling receptors, the regulatory events that control these protein machineries, and the functional consequences of these regulatory events. Research in the lab addresses fundamental questions in these areas using G protein-coupled signaling receptors (GPCRs) important in drug addiction as model signaling receptors.

Specific Projects

  1. Regulation of Endocytosis of Opioid Receptors by Addictive Drugs
    Activation of signaling receptors, including opioid receptors and related GPCRs, results in removal of activated receptors from the cell surface via endocytosis through clathrin-coated pits. Receptors were long thought to be passive ‘cargo’ in the endocytic pathway. Our recent data, however, suggest that receptors play a more active role in controlling their own destiny, by specifically regulating the kinetics of the subset of clathrin-coated pits that they use. We are investigating the mechanisms by which opioid receptors, activated by drugs, regulate endocytic kinetics. These mechanisms likely play a key role in drug addiction, as the amount of receptor endocytosis induced by drugs seem to be linked to their addictive potential.
  2. Sorting of Signaling Receptors in the Endosome
    Endocytosed receptors may be returned (or recycled) to the cell surface, thus allowing the cell to respond to the signal again (i.e., be ‘re-sensitized’ to the signal), or may be targeted to the lysosome to be destroyed, leading to prolonged ‘de-sensitization’ of the cell. Despite this clear significance to signaling, how different receptors are sorted into distinct trafficking pathways in the endosome is not known. We have identified a novel role for an actin-based machinery in selectively directing specific receptors to the recycling pathway, and are investigating the biochemical mechanism, regulation, and functional relevance of this machinery.
  3. Regulated Surface Insertion of Receptors from the Biosynthetic Pathway
    In the case of receptors that are sorted into the lysosome and destroyed, the cell is re-sensitized only when newly synthesized receptors are inserted on the plasma membrane from the biosynthetic pathway. While there is evidence that biosynthetic insertion of receptors is highly regulated in neurons, we know very little about the signaling mechanisms that regulate this insertion and their functional significance. We use the delta-opioid receptor, whose biosynthetic trafficking is regulated, as a model receptor to study the general principles, mechanisms, and functional consequences of regulated insertion of signaling receptors on the plasma membrane.

Publications

Soohoo AL, Bowersox SL, Puthenveedu MA. Visualizing Clathrin-mediated Endocytosis of G Protein-coupled Receptors at Single-event Resolution via TIRF Microscopy. J Vis Exp. 2014 Oct 20

Vistein R, Puthenveedu MA. Src regulates sequence-dependent beta-2 adrenergic receptor recycling via cortactin phosphorylation. Traffic. 2014 Jul 31. doi: 10.1111/tra.12202.

Shiwarski DJ, Shao C, Bill A, Kim J, Xiao D, Bertrand C, Seethala RR, Sano D, Myers JN, Ha PK, Grandis JR, Gaither LA, Puthenveedu MA, Duvvuri U. To "Grow" or "Go": TMEM16A Expression as a Switch between Tumor Growth and Metastasis in SCCHN. Clin Cancer Res. 2014 Jun 11. pii: clincanres.0363.2014.

Jean-Alphonse F, Bowersox S, Chen S, Beard G, Puthenveedu MA, Hanyaloglu AC. Spatially restricted G protein-coupled receptor activity via divergent endocytic compartments. J Biol Chem. 2014 Feb 14;289(7):3960-77

Vistein R, Puthenveedu MA. Reprogramming of G protein-coupled receptor recycling and signaling by a kinase switch. Proc Natl Acad Sci U S A. 2013 Sep 3. [Epub ahead of print]

Ryder PV, Vistein R, Gokhale A, Seaman MN, Puthenveedu M, Faundez V. The WASH Complex, an Endosomal Arp2/3 Activator, Interacts with the Hermansky-Pudlak Syndrome Complex BLOC-1 and its Cargo Phosphatidylinositol-4-kinase Type II Alpha. Mol Biol Cell. 2013 May 15.

Soohoo AL, Puthenveedu MA. Divergent modes for cargo-mediated control of clathrin-coated pit dynamics. Mol Biol Cell. 2013 Mar 27.

Puthenveedu MA, et al. Sequence-dependent sorting of recycling proteins by actin-stabilized endosomal microdomains. Cell. 143(5):761-73, 2010 Nov 24.

Yudowski GA*, Puthenveedu MA*, Henry AG, von Zastrow M. Cargo-mediated regulation of a rapid Rab4-dependent recycling pathway. Mol Biol Cell. 20(11):2774-84, 2009 Jun.
*denotes equal authorship

Yudowski GA*, Puthenveedu MA*, Leonoudakis D, Panicker S, Thorn KS, Beattie EC, von Zastrow M. Real-time imaging of discrete exocytic events mediating surface delivery of AMPA receptors. Journal of Neuroscience. 27(41):11112-21, 2007.
*denotes equal authorship

Puthenveedu MA, Yudowski GA, von Zastrow M. Endocytosis of neurotransmitter receptors: location matters. Cell. 130(6):988-9, 2007.

Shaw RM, Fay AJ, Puthenveedu MA, von Zastrow M, Jan YN, Jan LY. Microtubule plus-end-tracking proteins target gap junctions directly from the cell interior to adherens junctions. Cell. 128(3):547-60, 2007 Feb 9.

Puthenveedu MA, von Zastrow M. Cargo regulates clathrin-coated pit dynamics. Cell. 127(1):113-24, 2006.

Yudowski GA, Puthenveedu MA, von Zastrow M. Distinct modes of regulated receptor insertion to the somatodendritic plasma membrane. Nature Neuroscience. 9(5):622-7, 2006.

Full PubMed Listings