Many products of interest to the biotechnology industry are synthesized and secreted from specialized cell types. Among the most significant products are those having therapeutic application such as hormones, plasma proteins and enzymes produced by the endocrine and exocrine glands (for a survey on biopharmaceuticals see ref. 1). The production of many bio-products takes advantage of recombinant DNA technology to construct vectors designed for high-level expression and secretion of proteins. Remarkably, a variety of cultured mammalian cells have the capacity to synthesize and secrete a vast array of biologically active proteins that are normally produced only in highly-specialized cells. Despite the higher cost of production compared to bacteria, yeast or insect cells, protein expression in mammalian cells is often obligatory to produce proteins in an enzymatic or biologically active form. However, the particular requirements protein may have often limits the yield and reduces the quality of proteins produced in mammalian cells. In order to understand factors that affect the quality of proteins, it is necessary to consider what factors affect protein folding, processing and secretion from mammalian cells. Remarkable progress has been made during the past two decades in understanding the molecular basis for protein secretion. This article briefly describes how proteins are synthesized, processed and transported through the secretory pathway to the cell surface. Particular emphasis is focused on the early secretory pathway because this is frequently the rate-limiting step. Biotechnology can take advantage of our expanding knowledge of the secretory pathway in order to design new strategies to improve and optimize the secretion of high-quality recombinant proteins from mammalian cells.

Protein Synthesis and Secretion : Animal Cells / R.J. Kaufman, L. Popolo - In: Encyclopedia of Industrial Biotechnology : Bioprocess, Bioseparation, and Cell Technology / [a cura di] M.C. Flickinger. - Hoboken : Wiley, 2010 Apr. - ISBN 9780471799306. [10.1002/9780470054581.eib514]

Protein Synthesis and Secretion : Animal Cells

L. Popolo
Ultimo
2010

Abstract

Many products of interest to the biotechnology industry are synthesized and secreted from specialized cell types. Among the most significant products are those having therapeutic application such as hormones, plasma proteins and enzymes produced by the endocrine and exocrine glands (for a survey on biopharmaceuticals see ref. 1). The production of many bio-products takes advantage of recombinant DNA technology to construct vectors designed for high-level expression and secretion of proteins. Remarkably, a variety of cultured mammalian cells have the capacity to synthesize and secrete a vast array of biologically active proteins that are normally produced only in highly-specialized cells. Despite the higher cost of production compared to bacteria, yeast or insect cells, protein expression in mammalian cells is often obligatory to produce proteins in an enzymatic or biologically active form. However, the particular requirements protein may have often limits the yield and reduces the quality of proteins produced in mammalian cells. In order to understand factors that affect the quality of proteins, it is necessary to consider what factors affect protein folding, processing and secretion from mammalian cells. Remarkable progress has been made during the past two decades in understanding the molecular basis for protein secretion. This article briefly describes how proteins are synthesized, processed and transported through the secretory pathway to the cell surface. Particular emphasis is focused on the early secretory pathway because this is frequently the rate-limiting step. Biotechnology can take advantage of our expanding knowledge of the secretory pathway in order to design new strategies to improve and optimize the secretion of high-quality recombinant proteins from mammalian cells.
secretion ; protein trafficking ; endoplasmic reticulum ; Golgi apparatus ; posttranslational modifications ; proteolytic processing ; unfolded protein response ; protein folding
Settore BIO/11 - Biologia Molecolare
apr-2010
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/153937
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