Toagosei Company, Ltd.

Nagoya University

Kyoto University

Keio University

Other

Seiko Epson Corporation

Hokkaido University

Lightron Co., Ltd.

Toa Gosei Kabushiki Kaisha

The University of Tokyo

University Public Corporation Osaka

Japan Tissue Engineering Co., Ltd.

Lightron International Co. Ltd.

National University Corporation Nagoya

Tetsuhiko Yoshida

Nahoko Baileykobayashi

Nahoko Kobayashi

Makoto Sawada

Mikio Niwa

Kenichi Tanaka

Yoshinori Yoshida

Hiroki Kourai

Yoshinao Yamada

Ayato Takada

Ikuhiko Nakase

Hitoshi Fukushima

Jun Kudo

Mitsuo Eguchi

Masato Hanamura

Masaji Okamoto

Ken-ichiro Hata

Masatoki Watanabe

Masayoshi Kume

Kenji Oosawa

Nobuaki Obata

Kazuhisa Chonabayashi

Yuki Kobayashi

Chikara Shinohara

Hiroshi Kanno

Nobuyoshi Shimizu

Takanori Sato

Atsushi Takayanagi

Yoko Matsuda

Jun Kudoh

Noriko Usami

Shuichi Asakawa

Rina Hashimoto

Kazuo Takayama

Tamami Adachi

Yasuhiro Tonoyama

Kosuke Noguchi

Tomoko Naoe

Tomohiro Izumiyama

Ken-Ichiro Hata

Sawada Makoto

Izumiyama Tomohiro

Junichi Masuda

The herein disclosed method for introducing a foreign substance of interest from outside a eukaryotic cell into at least a cytoplasm of the cell, comprises: (1) a step of preparing a foreign substance introduction construct that has a carrier peptide fragment comprising either of the amino acid sequences: KKRTLRKSNRKKRWPC(SEQ ID NO: 1) and KKRTLRKKKRKKRWPC(SEQ ID NO: 2), and that has the foreign substance of interest bonded to an N-terminal side and/or C-terminal side of the carrier peptide fragment; (2) a step of supplying the foreign substance introduction construct into a sample that contains a target eukaryotic cell; and (3) a step of incubating the sample into which the foreign substance introduction construct has been supplied, to thereby introduce the construct into the eukaryotic cell in the sample.

Foreign substance introduction construct and use thereof

The present disclosure provides a synthetic peptide containing an amino acid sequence that can be used to produce antibodies against proteins derived from a new coronavirus (SARS-CoV-2). The synthetic peptide provided herein is recognized as an antigen relative to at least one mammal, contains an amino acid sequence which is LNESLIDLQELGKYEQYIKWP (SEQ ID NO: 1), and has a total number of amino acid residues of 25 or less.

Amino acid sequence derived from S protein of SARS-CoV2 for generating an anti-SARS-CoV-2 antibody

The present disclosure provides siRNA that suppresses proliferation of new coronaviruses (SARS-CoV-2). The siRNA disclosed herein includes: a sense strand; and an antisense strand. The sense strand includes a target sequence comprising 19 to 23 bases in which a base at a 5' terminal is guanine (G) or cytosine (C), and an overhang comprising 2 to 4 bases added to a 3′ terminal side of the target sequence. The antisense strand includes a sequence complementary to the target sequence, and an overhang comprising 2 to 4 bases added to a 3′ terminal side of the complementary sequence. Here, at least a part of the target sequence contains at least a part of a base sequence encoding a signal peptide region of a spike protein (S protein) of SARS-CoV-2.

siRNA based on RNA sequence of SARS-CoV-2 and use thereof

An antitumor peptide provided according to the present invention includes

Antitumor peptide and use thereof

According to the present disclosure, a technology for efficiently introducing a desired foreign substance from the outside of eukaryotic cells into at least the cytoplasm (and the nucleolus) of the cells is provided. A method disclosed here includes a step of preparing a construct for introducing a foreign substance including a carrier peptide fragment composed of any of amino acid sequences: KKRTLRKKKRKKR (SEQ ID NO: 1), KKRTLRKRRRKKR (SEQ ID NO: 2), KKRTLRKRKRKKR (SEQ ID NO: 3) and KKRTLRKKRRKKR (SEQ ID NO: 4), and a foreign substance that is bound to an N-terminal side and/or C-terminal side of the carrier peptide fragment, a step of supplying the construct for introducing a foreign substance to a sample containing desired eukaryotic cells, and a step of incubating the sample to which the construct for introducing a foreign substance is supplied and introducing the construct into eukaryotic cells in the sample.

Carrier peptide fragment for nucleolar localization and use thereof

The present disclosure provides an artificially synthesized peptide fragment that can efficiently introduce a foreign substance of interest from outside a eukaryotic cell into at least the cytoplasm of the cell. The present disclosure also provides a method for using the peptide fragment. The herein disclosed peptide fragment is a peptide fragment for introducing a foreign substance of interest from outside a eukaryotic cell into at least the cytoplasm of the cell, and is provided with a repeat sequence in which the VVRSLVK amino acid sequence (SEQ ID NO: 1) is repeated at least two or more times. By using a construct that has the peptide fragment and the foreign substance of interest bonded to the N-terminal side and/or C-terminal side of the peptide fragment, the foreign substance of interest can be efficiently introduced from outside a eukaryotic cell into at least the cytoplasm of the cell.

Carrier peptide fragment and use thereof

The synthetic peptide disclosed herein is a synthetic peptide which is artificially synthesized for suppressing binding of CTLA4 to at least one of B7 proteins B7-1 and B7-2. The synthetic peptide includes a CTLA4-B7 protein binding inhibitory peptide sequence. The CTLA4-B7 protein binding inhibitory peptide sequence is any one of amino acid sequences shown in the following (1) to (3): (1) a TIM3-SP-related sequence; (2) an LAGS-SP-related sequence; and (3) a CTLA4-SP-related sequence. Here, the total number of amino acid residues in the above-described synthetic peptide is 100 or less.

Peptide suppressing binding of CTLA4 to B7 proteins, and use thereof

The synthetic peptide disclosed here includes (1) an amino acid sequence represented by any of SEQ ID NOS:1 to 10, or a modified amino sequence formed by deletion, substitution or addition of 1, 2 or 3 amino acid residues in any of these amino acid sequences, together with (2) an amino acid sequence (CPP sequence) that functions as a cell penetrating peptide (CPP), and consists of a total of not more than 100 amino acid residues.

Antiviral peptide and use thereof

A synthetic peptide provided according to the technology disclosed here includes

An antitumor peptide provided according to the present invention includes (1) an S1PR-TM related sequence; and (2) an amino acid sequence functioning as a cell penetrating peptide; wherein the total number of amino acid residues is 100 or less.

A synthetic peptide provided by the present invention includes: (1) a CTLA4-SP-related sequence; and (2) an amino acid sequence that functions as a cell penetrating peptide, wherein the synthetic peptide has a total number of amino acid residues of 100 or less.

Provided is a method for producing myocardial cells from pluripotent stem cells. The myocardial cell production method provided by the present invention includes supplying an artificially produced synthetic peptide to a cell culture that contains pluripotent stem cells. The synthetic peptide is a peptide that contains a myocardial cell differentiation-inducing peptide sequence that induces pluripotent stem cells into myocardial cells. The myocardial cell differentiation-inducing peptide sequence is an amino acid sequence selected from the group consisting of (i) an amino acid sequence constituting the signal peptide of any protein belonging to the amyloid precursor protein (APP) family, (ii) a partial amino acid sequence of the amino acid sequence according to (i), and (iii) a modified amino acid sequence from the amino acid sequence according to (i) or (ii).

Method for producing myocardial cells using synthetic peptide

Provide is an artificially synthesized antitumor peptide that may suppress proliferation of tumor cells. The peptide provided is a synthetic peptide that contains both (1) an amino acid sequence that forms a signal peptide of a membrane protein, programmed cell death-1 (PD-1), or a modified amino acid sequence thereof in which 1, 2 or 3 amino acid residues deleted from, substituted in or added to the above amino acid sequence; and (2) an amino acid sequence that serves as a cell penetrating peptide (CPP), and wherein the synthetic peptide comprises a total of 100 or fewer amino acid residues.

Antitumor peptide having PD-1 signal sequence and utilization thereof

The antitumor peptide provided by the present invention is a synthetic peptide including both of:

Provided is a novel material used to introduce an exogenous substance into cells. Also provided is a method for introducing an exogenous substance into target cells using this material. The present invention provides an exosome that is used to introduce an exogenous substance into target cells, wherein the exosome contains one type or two or more types of an exogenous substance and a substance that induces macropinocytosis in the target cells. The present invention also provides a composition containing the exosome and a method for introducing an exogenous substance into cells using this exosome.

Method for introducing exogenous substance into cell, and material used in said method

Growing community of inventors

Tsukuba, Japan

Tetsuhiko Yoshida