Patents by Inventor Nahoko Kobayashi

Nahoko Kobayashi 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: 20090030179
    Abstract: Antimicrobial peptides provided by the present invention are artificially designed antimicrobial peptides that are not present in nature. Several antimicrobial peptides have, as the amino acid sequence related to the expression of antimicrobial property, a partial amino acid sequence in the ?-domain of human-derived VHL protein. In addition, several antimicrobial peptides have a partial amino acid sequence of SOCS-box of a certain SOCS-box protein.
    Type: Application
    Filed: February 14, 2006
    Publication date: January 29, 2009
    Applicant: TOAGOSEI CO., LTD
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi
  • Publication number: 20090012000
    Abstract: Disclosed is an anti-viral peptide which non-naturally occurs and is artificially synthesized. The peptide has at least one unit of the following amino acid sequence (a) and at least one unit of the following amino acid sequence (b) or (c): (a) 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; (b) a conserved sequence of VAP which is an endoplasmic reticulum protein or an amino acid sequence having a partial modification in the conserved sequence; and (C) an amino acid sequence which is known as a FFAT motif found in various lipid-binding proteins or an amino acid sequence having a partial modification in the amino acid sequence.
    Type: Application
    Filed: May 1, 2007
    Publication date: January 8, 2009
    Applicant: TOAGOSEI CO., LTD.
    Inventors: Tetsuhiko Yoshida, Nahoko Kobayashi, Takanori Sato
  • Patent number: 7176276
    Abstract: An object of the invention is to provide an antimicrobial peptide having an amino acid sequence which is different from a peptide existing and functioning as an antimicrobial peptide in the natural world and is not based on the conventional developmental approach for an antimicrobial peptide-containing antimicrobial agent, and a polynucleotide coding for said peptide. Another object is to provide an antimicrobial agent which contains such an antimicrobial peptide. Namely, an antimicrobial peptide represented by a general formula (1) (Xa)n-S??(1) wherein Xa of the formula (1) is a hydrophilic amino acid residue, n is an integer of from 1 to 6, two or more of the Xa may be the same or different from one another, S is a peptide represented by hydrophobic amino acid part-basic amino acid part-bridge part-basic amino acid part-hydrophobic amino acid part, and amino acid residue of the bridge part is selected from the group consisting of hydrophobic amino acids and neutral amino acids.
    Type: Grant
    Filed: May 25, 2004
    Date of Patent: February 13, 2007
    Assignees: Toagosei Co., Ltd.
    Inventors: Hiroki Kourai, Takuya Maeda, Hideaki Nagamune, Nahoko Kobayashi
  • Publication number: 20060122122
    Abstract: Antimicrobial agent including an artificially synthesized antimicrobial peptide that does not occur naturally is provided by present invention. The peptide included in the antimicrobial agent includes 1 unit, 2 units or more units of sequence(s) or sequence(s) with partial modification, the sequence(s) composed of at least 6 contiguous amino acid residues selected from any one of amino acid sequences: (a) KVQIINKK; (b) SVQIVYKP; (c) QVEVKSEK; (d) KKVAVVRT; (e) KKVAIIRT; (f) KKPTSAK, and the total number of amino acid residues included in 1 unit, 2 units or more units of sequence(s) is 30% or more of the total number of amino acid residues constituting the peptide chain.
    Type: Application
    Filed: December 5, 2005
    Publication date: June 8, 2006
    Applicant: Toagosei Co., Ltd.
    Inventors: Nahoko Kobayashi, Tetsuhiko Yoshida
  • Publication number: 20060089488
    Abstract: Artificially synthesized antimicrobial peptide that does not occur naturally is provided by the present invention. The antimicrobial peptide includes one unit, two units or more units of amino acid sequence composed of the following 8 amino acid residues: (R or Q)-(L or F or I)—I—K-(L or F or I or V)-L-Y-Q; and/or, modified sequence composed of said sequence with partial modification.
    Type: Application
    Filed: October 11, 2005
    Publication date: April 27, 2006
    Applicant: Toagosei Co., Ltd.
    Inventors: Tetsuhiko Yoshida, Yoshinao Yamada, Nahoko Kobayashi, Hiroki Kourai
  • Publication number: 20050171335
    Abstract: An object of the invention is to provide an antimicrobial peptide having an amino acid sequence which is different from a peptide existing and functioning as an antimicrobial peptide in the natural world and is not based on the conventional developmental approach for an antimicrobial peptide-containing antimicrobial agent, and a polynucleotide coding for said peptide. Another object is to provide an antimicrobial agent which contains such an antimicrobial peptide. Namely, an antimicrobial peptide represented by a general formula (1) (Xa)n-S??(1) wherein Xa of the formula (1) is a hydrophilic amino acid residue, n is an integer of from 1 to 6, two or more of the Xa may be the same or different from one another, S is a peptide represented by hydrophobic amino acid part-basic amino acid part-bridge part-basic amino acid part-hydrophobic amino acid part, and amino acid residue of the bridge part is selected from the group consisting of hydrophobic amino acids and neutral amino acids.
    Type: Application
    Filed: May 25, 2004
    Publication date: August 4, 2005
    Inventors: Hiroki Kourai, Takuya Maeda, Hideaki Nagamune, Nahoko Kobayashi