Patents by Inventor Tetsuhiko Yoshida

Tetsuhiko Yoshida has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20140335613
    Abstract: The pharmaceutical composition provided by the present invention comprises at least one pharmaceutically acceptable carrier, and an active ingredient including an artificially synthesized peptide comprises: (A) an amino acid sequence constituting a cell-penetrating peptide and (B) an amino acid sequence constituting the signal peptide in amyloid precursor protein (APP) or an N-terminal partial amino acid sequence or C-terminal partial amino acid sequence from the amino acid sequence constituting that signal peptide.
    Type: Application
    Filed: July 25, 2014
    Publication date: November 13, 2014
    Inventors: Tetsuhiko YOSHIDA, Nahoko KOBAYASHI
  • Patent number: 8822408
    Abstract: The pharmaceutical composition includes at least one pharmaceutically acceptable carrier, and an active ingredient including an artificially synthesized peptide includes: (A) an amino acid sequence constituting a cell-penetrating peptide and (B) an amino acid sequence constituting the signal peptide in amyloid precursor protein (APP) or an N-terminal partial amino acid sequence or C-terminal partial amino acid sequence from the amino acid sequence constituting that signal peptide.
    Type: Grant
    Filed: June 3, 2011
    Date of Patent: September 2, 2014
    Assignee: Toagosei Co., Ltd.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi
  • Publication number: 20140178990
    Abstract: A method for manufacturing at least one kind of eukaryotic cells or a biosynthetic substance derived from the eukaryotic cells by proliferating the cells, which includes preparing an artificially synthesized peptide for promoting proliferation of the at least one kind of eukaryotic cells, incubating the eukaryotic cells in a culture medium, and adding the synthesized peptide at least once to the culture medium during the incubation process. The synthesized peptide includes an amino acid sequence selected from SEQ ID NOS: 1 to 18, and an amino acid sequence selected from SEQ ID NOS: 19 to 97.
    Type: Application
    Filed: January 24, 2014
    Publication date: June 26, 2014
    Applicants: JAPAN TISSUE ENGINEERING CO., LTD., TOAGOSEI CO. LTD.
    Inventors: Tetsuhiko YOSHIDA, Nahoko KOBAYASHI, Mikio NIWA, Chikara SHINOHARA, Masatoki WATANABE, Ken-ichiro HATA
  • Patent number: 8710005
    Abstract: A neuronal differentiation inducer provided by the present invention contains an artificially synthesized peptide which includes an amino acid sequence constituting a signal peptide in amyloid precursor protein (APP), or a partial sequence of the amino acid sequence constituting this signal peptide.
    Type: Grant
    Filed: April 12, 2010
    Date of Patent: April 29, 2014
    Assignee: Toagosei Co., Ltd.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi
  • Patent number: 8673846
    Abstract: A cell proliferation promoter includes, as an active ingredient, an artificially synthesized peptide that includes (A) an amino acid sequence constituting a membrane-permeable peptide and (B) an amino acid sequence selected from SEQ ID NOs: 19 to 103 or an amino acid sequence formed by substituting, deleting and/or adding one or several amino acid residues in the selected amino acid sequence.
    Type: Grant
    Filed: October 28, 2010
    Date of Patent: March 18, 2014
    Assignees: Toagosei Co. Ltd., Japan Tissue Engineering Co., Ltd.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi, Mikio Niwa, Chikara Shinohara, Masatoki Watanabe, Ken-ichiro Hata
  • Patent number: 8673845
    Abstract: The method for transferring a foreign substance provided by the present invention includes the steps of: preparing a construct for transferring a foreign substance that contains a carrier peptide fragment including either the amino acid sequence WRRQARFK (SEQ ID NO. 1) or any amino acid sequence formed by the substitution, deletion, and/or addition (insertion) of 1, 2, or 3 amino acid residues in the amino acid sequence, and a foreign substance of interest that is bonded to the N-terminus and/or C-terminus of the carrier peptide fragment; supplying the construct for transferring a foreign substance to a test sample that contains a target eukaryotic cell; and incubating the test sample that has been supplied with the construct for transferring a foreign substance to thereby transfer the construct into the eukaryotic cell in the test sample.
    Type: Grant
    Filed: July 28, 2010
    Date of Patent: March 18, 2014
    Assignee: Toagosei Co., Ltd.
    Inventors: Nahoko Kobayashi, Tetsuhiko Yoshida, Mikio Niwa, Kenichi Tanaka
  • Publication number: 20140072592
    Abstract: The object of the present invention is to provide a method to obtain an antibody for a hydrophobic peptide, which can be used for general purposes easily and with great reliability. Also provided is a method for preparing an antigen characterized in that a hydrophobic peptide, which is unbound to carrier protein, is used as high-molecular-weight aggregates in an aqueous solution containing a nonionic surfactant.
    Type: Application
    Filed: January 6, 2012
    Publication date: March 13, 2014
    Applicants: SEIKO EPSON CORPORATION, TOAGOSEI CO., LTD.
    Inventors: Masaji Okamoto, Masato Hanamura, Hitoshi Fukushima, Tetsuhiko Yoshida
  • Publication number: 20140051647
    Abstract: This invention provides a TNFR2 expression-inducing composition including as an active ingredient a peptide having TNFR2 expression-inducing activity, and a method for producing cells that express TNFR2 selectively by use of the composition. The cell production method provided by this invention includes: culturing at least one species of cells capable of expressing TNF receptor 2, and supplying the cells with a synthetic peptide consisting of a nuclear localization signal sequence (NLS) or a nucleolar localization signal sequence (NoLS) to enhance TNFR2 expression in the cells.
    Type: Application
    Filed: April 17, 2012
    Publication date: February 20, 2014
    Applicant: TOAGOSEI CO. LTD.
    Inventors: Nahoko Kobayashi, Tetsuhiko Yoshida, Mikio Niwa
  • Publication number: 20130345408
    Abstract: An advantage of some aspects of the invention is to provide an antibody against an amyloid precursor protein signal peptide. The invention provides an amyloid precursor protein signal peptide.
    Type: Application
    Filed: January 6, 2012
    Publication date: December 26, 2013
    Applicants: TOAGOSEI CO. LTD., SEIKO EPSON CORPORATION
    Inventors: Hitoshi Fukushima, Masato Hanamura, Mikio Niwa, Masaji Okamoto, Tomoko Naoe, Tetsuhiko Yoshida
  • Patent number: 8603967
    Abstract: A method for transferring a foreign substance includes the steps of: preparing a construct for transferring a foreign substance that contains a carrier peptide fragment including either the amino acid sequence KKRTLRKNDRKKR (SEQ ID NO. 1) or an amino acid sequence formed by the substitution, deletion, and/or addition (insertion) of 1, 2, or 3 amino acid residues in the amino acid sequence, and a foreign substance of interest that is bonded to the N-terminus and/or C-terminus of the carrier peptide fragment; supplying the construct for transferring a foreign substance to a test sample that contains a target eukaryotic cell; and incubating the test sample that has been supplied with the construct for transferring a foreign substance to thereby transfer the construct into the eukaryotic cell in the test sample.
    Type: Grant
    Filed: July 28, 2010
    Date of Patent: December 10, 2013
    Assignee: Toagosei Co., Ltd.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi, Mikio Niwa
  • Publication number: 20130323776
    Abstract: A method for transferring a foreign substance includes: preparing a construct for transferring a foreign substance that contains a carrier peptide fragment including any amino acid sequence selected from SEQ ID NOS: 1-6, or an amino acid sequence formed by the substitution, deletion, and/or addition (insertion) of 1, 2, or 3 amino acid residues in the amino acid sequence of the selected sequence identification number, and a foreign substance of interest that is bonded to the N-terminus and/or C-terminus of the carrier peptide fragment; supplying the construct for transferring a foreign substance to a test sample that contains a target eukaryotic cell; and incubating the test sample that has been supplied with the construct for transferring a foreign substance to thereby transfer the construct into the eukaryotic cell in the test sample.
    Type: Application
    Filed: July 8, 2013
    Publication date: December 5, 2013
    Inventors: Tetsuhiko YOSHIDA, Nahoko KOBAYASHI, Mikio NIWA, Kenichi TANAKA
  • Publication number: 20130142812
    Abstract: A cell growth inhibitor that includes, as an antibody component, an artificially produced anti-EGFR antibody having specific binding capacity to EGFR which is characterized in that an epitope therefor is in a cysteine-rich subdomain 2 (C2 domain) and/or in a ligand-binding domain 1 (L1 domain) among four subdomains contained in the extracellular domain of EGFR.
    Type: Application
    Filed: June 3, 2011
    Publication date: June 6, 2013
    Applicants: KEIO UNIVERSITY, TOAGOSEI CO. LTD.
    Inventors: Nobuyoshi Shimizu, Atsushi Takayanagi, Tetsuhiko Yoshida
  • Publication number: 20130079273
    Abstract: The pharmaceutical composition includes at least one pharmaceutically acceptable carrier, and an active ingredient including an artificially synthesized peptide includes: (A) an amino acid sequence constituting a cell-penetrating peptide and (B) an amino acid sequence constituting the signal peptide in amyloid precursor protein (APP) or an N-terminal partial amino acid sequence or C-terminal partial amino acid sequence from the amino acid sequence constituting that signal peptide.
    Type: Application
    Filed: June 3, 2011
    Publication date: March 28, 2013
    Applicant: TOAGOSEI CO. LTD.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi
  • Publication number: 20130005034
    Abstract: Disclosed is a method for transforming human or non-human mammalian stem cells by introducing a desired peptide motif into the stem cells. The stem cell transformation method disclosed herein uses a synthesized peptide having an amino acid sequence which constitutes the desired peptide motif on the N-terminal end or C-terminal end of a cell membrane-permeable nucleolar localization signal sequence defined by the amino acid sequence KKRTLRKNDRKKR (SEQ ID NO:1).
    Type: Application
    Filed: September 12, 2012
    Publication date: January 3, 2013
    Applicant: TOAGOSEI CO., LTD
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi, Junichi Masuda
  • Publication number: 20120208752
    Abstract: A cell proliferation promoter includes, as an active ingredient, an artificially synthesized peptide that includes (A) an amino acid sequence constituting a membrane-permeable peptide and (B) an amino acid sequence selected from SEQ ID NOs: 19 to 103 or an amino acid sequence formed by substituting, deleting and/or adding one or several amino acid residues in the selected amino acid sequence.
    Type: Application
    Filed: October 28, 2010
    Publication date: August 16, 2012
    Applicants: JAPAN TISSUE ENGINEERING CO., LTD., TOAGOSEI CO. LTD.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi, Mikio Niwa, Chikara Shinohara, Masatoki Watanabe, Ken-ichiro Hata
  • Publication number: 20120149053
    Abstract: A method for transferring a foreign substance includes the steps of: preparing a construct for transferring a foreign substance that contains a carrier peptide fragment including any amino acid sequence selected from SEQ ID Nos. 1, 2, 3, 4, 5, and 6, or an amino acid sequence formed by the substitution, deletion, and/or addition (insertion) of 1, 2, or 3 amino acid residues in the amino acid sequence of the selected sequence identification number, and a foreign substance of interest that is bonded to the N-terminus and/or C-terminus of the carrier peptide fragment; supplying the construct for transferring a foreign substance to a test sample that contains a target eukaryotic cell; and incubating the test sample that has been supplied with the construct for transferring a foreign substance to thereby transfer the construct into the eukaryotic cell in the test sample.
    Type: Application
    Filed: July 28, 2010
    Publication date: June 14, 2012
    Applicant: TOAGOSEI CO. LTD.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi, Mikio Niwa, Kenichi Tanaka
  • Publication number: 20120122225
    Abstract: The method for transferring a foreign substance provided by the present invention includes the steps of: preparing a construct for transferring a foreign substance that contains a carrier peptide fragment including either the amino acid sequence WRRQARFK (SEQ ID NO. 1) or any amino acid sequence formed by the substitution, deletion, and/or addition (insertion) of 1, 2, or 3 amino acid residues in the amino acid sequence, and a foreign substance of interest that is bonded to the N-terminus and/or C-terminus of the carrier peptide fragment; supplying the construct for transferring a foreign substance to a test sample that contains a target eukaryotic cell; and incubating the test sample that has been supplied with the construct for transferring a foreign substance to thereby transfer the construct into the eukaryotic cell in the test sample.
    Type: Application
    Filed: July 28, 2010
    Publication date: May 17, 2012
    Applicant: TOAGOSEI CO. LTD.
    Inventors: Nahoko Kobayashi, Tetsuhiko Yoshida, Mikio Niwa, Kenichi Tanaka
  • Publication number: 20120122210
    Abstract: A method for transferring a foreign substance includes the steps of: preparing a construct for transferring a foreign substance that contains a carrier peptide fragment including either the amino acid sequence KKRTLRKNDRKKR (SEQ ID NO. 1) or an amino acid sequence formed by the substitution, deletion, and/or addition (insertion) of 1, 2, or 3 amino acid residues in the amino acid sequence, and a foreign substance of interest that is bonded to the N-terminus and/or C-terminus of the carrier peptide fragment; supplying the construct for transferring a foreign substance to a test sample that contains a target eukaryotic cell; and incubating the test sample that has been supplied with the construct for transferring a foreign substance to thereby transfer the construct into the eukaryotic cell in the test sample.
    Type: Application
    Filed: July 28, 2010
    Publication date: May 17, 2012
    Applicant: TOAGOSEI CO. LTD.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi, Mikio Niwa
  • Patent number: 8138146
    Abstract: Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES.
    Type: Grant
    Filed: February 28, 2007
    Date of Patent: March 20, 2012
    Assignee: Toagosei Co., Ltd
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi, Takanori Sato
  • Publication number: 20120035112
    Abstract: A neuronal differentiation inducer provided by the present invention contains an artificially synthesized peptide which includes an amino acid sequence constituting a signal peptide in amyloid precursor protein (APP), or a partial sequence of the amino acid sequence constituting this signal peptide.
    Type: Application
    Filed: April 12, 2010
    Publication date: February 9, 2012
    Applicant: Toagosei Co., Ltd.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi