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Takeo
Iwamoto
Research Assistant Professor, Associate Director, Biotechnology Core Facility Sr. Scientist - Nacelle Therapeutics
The
Tomich laboratory designs and characterizes synthetic peptides for
potential uses as drugs or renewable biomaterials. The lab employs a
number of biologic, synthetic, analytic and physical methods to make
these characterizations.
B.S. 1982, Tokyo University of Pharmacy, Japan
Ph.D. 1988, Tokyo Institute of Technology
Phone: 785-532-5956
Fax: 785-532-7278
Email: iwamoto@k-state.edu
Office: 214 Burt Hall |
| 1982-1990 |
Research Associate, The Jikei University School of Medicine, Tokyo, Japan. Keiji Iriyam Supervisor. |
| 1990-1992 |
Ph.D. Research Fellow, Department of Biochemistry,
University of Southern California School of Medicine, Los Angeles,
California. John M. Tomich, Supervisor. |
| 1992-1998 |
Assistant Director Biotechnology Core Facility, Kansas State University, Manhattan, Kansas |
| 1999-present |
Research Assistant Professor of Biochemistry, Kansas State University, Manhattan, Kansas |
| 1999-present |
Associate Director, Biotechnology Core Facility, Kansas State University, Manhattan, Kansas |
| 2002-present |
Senior Scientist, Nacelle Therapeutics, Inc. Manhattan, Kansas |
Selected
Publications
Smith, E., Tomich, J. M., Iwamoto, T., Richards, J. H. and Feinberg,
B. (1991) A totally synthetic histidine-2 ferredoxin:
Thermal stability and redox properties. Biochemistry 30,
11669-11676.
Nozawa, M., Iwamoto, T., Tokoro, T., and Eto, Y. (1992) Novel
procedure for measuring psychosine derivatives by an HPLC method.
J. Neurochem. 59, 607-609.
Montal, M. S., Iwamoto, T., Tomich, J. M. and Montal, M.
(1993) Design, synthesis and functional characterization of a
pentameric channel protein that mimics the presumed pore structure of
the nicotinic cholinergic receptor. FEBS Lett. 320, 261-266.
Montal, M. O., Bühler, L., Iwamoto, T., Tomich, J. M. and Montal,
M. (1993) Synthetic peptides and four-helix bundle proteins
as model systems for the pore-forming structure of channel proteins.
Transmembrane segment M2 of the nicotinic cholinergic receptor channel
is a key pore lining structure. J. Biol. Chem., 268,
14601-07.
Reddy, L. G., Iwamoto, T., Tomich, J. M. and Montal, M.
(1993) Synthetic peptides and four-helix bundle proteins as model
systems for the pore-forming structure of channel proteins.
Transmembrane segment M2 of the brain glycine receptor channel is a
plausible candidate for the pore-lining structure. J. Biol.
Chem., 268, 14608-15.
Grove, A., Tomich, J. M., Iwamoto, T. and Montal, M. (1993)
Design of a functional calcium channel protein: Inferences about
an ion channel forming motif derived from the primary structure of
voltage-gated calcium channels. Protein Sci. 2, 1918-1930.
Montal, M. O., Reddy, L. G., Iwamoto, T., Tomich, J. M. and Montal,
M. (1994) Identification of an ion channel-forming motif in
the primary structure of CFTR, the cystic fibrosis chloride
channel. Proc. Natl. Acad. Sci. USA. 91, 1495-1499.
Iwamoto, T., Grove, A., Oblatt-Montal, M., Montal, M. and Tomich, J.
M. (1994) Chemical synthesis and characterization of
peptides and oligomeric proteins designed to form transmembrane ion
channels. Int. J. Pept. Prot. Res. 43, 597-607.
Shi MM, Kugelman A, Iwamoto T, Tian L, Forman HJ. Quinone-induced
oxidative stress elevates glutathione and induces
gamma-glutamylcysteine synthetase activity in rat lung epithelial L2
cells. J Biol Chem. 1994 Oct 21;269(42):26512-7.
Shi MM, Iwamoto T, Forman HJ. gamma-Glutamylcysteine synthetase and GSH
increase in quinone-induced oxidative stress in BPAEC. Am J Physiol.
1994 Oct;267(4 Pt 1):L414-21.
Rajagopalan, S., Heck, T. J., Iwamoto, T. and Tomich, J. M.
(1995) Use of the 3-nitro-2-pyridine sulfenyl protecting group to
introduce Ne-branching at lysine during solid-phase peptide
synthesis: I. Application to the synthesis of a peptide template
containing two addressable sites. Intl. J. Prot. Pept. Res. 45,
173-179.
Forman HJ, Shi MM, Iwamoto T, Liu RM, Robison TW. Measurement of
gamma-glutamyl transpeptidase and gamma-glutamylcysteine synthetase
activities in cells. Methods Enzymol. 1995;252:66-71
Pandit, S. D., Donis-Keller, H., Iwamoto, T., Tomich, J. M., Pike, L.
J. (1996) The MEN 2B point mutation alters the transforming capacity of
the EGF receptor. J. Biol. Chem. 271, 5850-5858.
Wallace, D. P., Tomich, J. M., Iwamoto, T., Henderson, K., Grantham, J.
J. (1997) and Sullivan, L. P. A synthetic peptide derived from the
glycine-gated Cl- channel generates Cl- and fluid secretion by
epithelial monolayers. Am. J. Physiol: 272 (Cell Physiol. 41)
C1672-C1679.
Tomich, J. M., Wallace, D. P., Henderson, K., Brandt, R., Scott, A. J.,
Mitchell, K. E. Radke, G.,Grantham, J. J. Sullivan, L. P. &
Iwamoto, T. (1998) Aqueous solubilization of transmembrane peptide
sequences with retention of membrane insertion and function. Biophys
J. 74, 256-267.
Wallace, D. P., Tomich, J. M., Eppler, J., Iwamoto, T., Grantham, J.
J.and Sullivan, (2000) L. P. A Channel forming peptide induces
Cl- secretion by T84 cells: Modulation by Ca2+ - dependent K+
channels. Biochim. Biophys. Acta 1464, 69-82.
Mitchell, K. E., Tomich, J. M., Iwamoto, T. and Freeman, L.C.(2000) A
synthetic peptide based on a glycine-gated chloride channel induces a
novel chloride conductance in isolated epithelial cells. Biochim.
Biophys. Acta 1466, 47-60.
Broughman, J.R., Mitchell, K., Iwamoto, T., Tomich J.M. and Schultz,
B.D. (2001) Amino-terminal modification of a channel-forming
peptide increases capacity for epithelia anion secretion. Am. J.
Physiol. (Cell) 280, C451-C458.
Gao, L., Broughman, J.R., Iwamoto, T., Tomich, J.M., Venglarik, C.J.and
Forman, H.J. (2001) Synthetic Cl- channel restores glutathione
secretion in airway epithelia. Am.J.Physiol (Lung) 281 L24-L30.
Broughman JR, Shank LP, Takeguchi W, Iwamoto T, Mitchell KE, Schultz,
BD and Tomich JM. (2002) Distinct structural elements that direct
solution aggregation and membrane assembly in the channel forming
peptide M2GlyR. Biochemistry 41,7350-7358.
Broughman JR, Shank LP, Iwamoto T, Prakash O, Schultz BD, Tomich JM and
Mitchell KE (2002) Structural implications of placing cationic residues
at either the NH2- or COOH- terminus in a pore-forming synthetic
peptide. J Membrane Biol. 190: 93-103.
Dickinson DA, Iles KE, Watanabe N, Iwamoto T, Zhang H, Krzywanski DM,
Forman HJ.(2002) 4-hydroxynonenal induces glutamate cysteine ligase
through JNK in HBE1 cells. Free Radic Biol Med. 33:974.
Watanabe N, Iwamoto T, Dickinson DA, Iles KE, Forman HJ. (2002)
Activation of the mitochondrial caspase cascade in the absence of
protein synthesis does not require c-Jun N-terminal kinase. Arch
Biochem Biophys. 405(2):231-40.
Iles KE, Dickinson DA, Watanabe N, Iwamoto T, Forman HJ. (2002) AP-1
activation through endogenous H(2)O(2) generation by alveolar
macrophages. Free Radic Biol Med 32(12):1304-13. Erratum in: Free Radic
Biol Med. 33(5):725.
Matsumoto N, Tsuruoka S, Iwamoto T, Tomich JM, Ito K, Imai M and Suzuki
M. (2003) Alterations in Ion Transport Induced by an Artificial
Cl- Channel in Micro-Perfused Renal Proximal Tubules. J.
Membr. Biol. 193:195-200.
Watanabe N, Iwamoto T, Bowen KD, Dickinson DA, Torres M, Forman HJ.
(2003) Bio-effectiveness of Tat-catalase conjugate: a potential tool
for the identification of H2O2-dependent cellular signal transduction
pathways. Biochem Biophys Res Commun. 303(1):287-93.
Cook GA, Prakash O, Zhang K, Shank LP, Robbins, A, Gong Y-X, Iwamoto T,
Schultz, BD and Tomich JM. (2004) Activity and Structural Comparisons
of Solution Associating and Monomeric Channel-Forming Peptides Derived
from the Glycine Receptor M2 Segment. Biophysical J. 86: 1424-1435.
Broughman JR, Brandt, R., Hastings C, Iwamoto T, Tomich JM and Schultz
BD, (2004) Anion Channel-Forming Peptide Modulates
Transepithelial Electrical Conductance and Solute Permeability. Am. J.
Physiol: (Cell Physiol. ) 286: C1312-1323.
Iwamoto T, You M, Li E, Spangler J, Tomich JM, Hristova K (2005)
Synthesis And Initial Characterization Of Fgfr3 Transmembrane Domain:
Consequences Of Sequence Modifications. In Press BBA-Biomembranes
Broughman JR, Brandt, R., Hastings C, Iwamoto T, Tomich JM and Schultz
BD, (2004) Anion Channel Forming Peptide Modulates Transepithelial
Electrical Conductance and Solute Permeability. Am. J. Physiol: (Cell Physiol.) 286: C1312-1323
Cook GA, Prakash O, Zhang K, Shank LP, Robbins, A,, Gong Y-X, Iwamoto
T, Schultz, BD and Tomich JM. (2004) Activity and Structural
Comparisons of Solution Associating and Monomeric Channel-Forming
Peptides Derived from the Glycine Receptor M2 Segment. Biophysical J. 86: 1424-1435.
No Previous or Current Funding
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