- LAS VEGAS NV, US Steven D. DAVIN - Seattle WA, US Hoa Binh DO - Kirkland WA, US Leon F. GARCIA-MARTINEZ - Woodinville WA, US Geoffrey F. LEE - Mercer Island WA, US Ethan W. OJALA - Snohomish WA, US Mark YOUNG - Boulder CO, US John A. LATHAM - Seattle WA, US
Processes for producing and purifying recombinant proteins are disclosed. In particular, the present disclosure provides processes of producing and purifying multi-subunit proteins expressed in yeast or filamentous fungal cells. The production and/or purification of such proteins are monitored for impurities, preferably using lectin binding assays, such that one or more process parameters may be adjusted to maximize the amount of desired recombinant protein and minimize the amount of glycosylated impurities. The processes can also be monitored for other undesired product-associated impurities, such as aggregates and nucleic acids. In exemplary embodiments, the recombinant proteins are multi-subunit proteins, such as antibodies, the host cell is a yeast, such as , and the glycosylated impurity is a glycovariant of the desired recombinant polypeptide, such as an N-linked and/or O-linked glycovariant.
- LAS VEGAS NV, US Steven D. Davin - Seattle WA, US Hoa Binh Do - Kirkland WA, US Leon F. Garcia-Martinez - Woodinville WA, US Geoffrey F. Lee - Mercer Island WA, US Ethan W. Ojala - Snohomish WA, US Mark Young - Boulder CO, US John A. Latham - Seattle WA, US
Processes for producing and purifying recombinant proteins are disclosed. In particular, the present disclosure provides processes of producing and purifying multi-subunit proteins expressed in yeast or filamentous fungal cells. The production and/or purification of such proteins are monitored for impurities, preferably using lectin binding assays, such that one or more process parameters may be adjusted to maximize the amount of desired recombinant protein and minimize the amount of glycosylated impurities. The processes can also be monitored for other undesired product-associated impurities, such as aggregates and nucleic acids. In exemplary embodiments, the recombinant proteins are multi-subunit proteins, such as antibodies, the host cell is a yeast, such as , and the glycosylated impurity is a glycovariant of the desired recombinant polypeptide, such as an N-linked and/or O-linked glycovariant.
- Las Vegas NV, US Steven D. DAVIN - Seattle WA, US Hoa Binh DO - Kirkland WA, US Leon F. GARCIA-MARTINEZ - Woodinville WA, US Geoffrey F. LEE - Mercer Island WA, US Ethan W. OJALA - Snohomish WA, US Mark YOUNG - Boulder CO, US John A. LATHAM - Seattle WA, US
Assignee:
ALDERBIO HOLDINGS LLC - Las Vegas NV
International Classification:
C07K 1/22 C07K 16/18
US Classification:
5303871, 530417, 435 691, 435 696
Abstract:
Processes for producing and purifying recombinant proteins are disclosed. In particular, the present disclosure provides processes of producing and purifying multi-subunit proteins expressed in yeast or filamentous fungal cells. The production and/or purification of such proteins are monitored for impurities, preferably using lectin binding assays, such that one or more process parameters may be adjusted to maximize the amount of desired recombinant protein and minimize the amount of glycosylated impurities. The processes can also be monitored for other undesired product-associated impurities, such as aggregates and nucleic acids. In exemplary embodiments, the recombinant proteins are multi-subunit proteins, such as antibodies, the host cell is a yeast, such as , and the glycosylated impurity is a glycovariant of the desired recombinant polypeptide, such as an N-linked and/or O-linked glycovariant.
2006 to 2000 Administrative AssistantMacau Casino Tukwila, WA Sep 2011 to Jun 2013 Cage/CashierTran's Accounting and Tax Service Seattle, WA Jan 2007 to Nov 2008 Paralegal Secretary
Education:
University of Washington Tacoma Tacoma, WA 2013 Bachelor of Art in Communication