Heterologous Protein Production Using The Twin Arginine Translocation Pathway

Abstract

Provided are means for evaluating and identifying putative substrates of the twin arginine translocation (Tat) secretory pathway in Streptomyces and other bacterial species. Also provided, therefore, are simple ways to express, secrete and purify correctly folded heterologous proteins on a large scale using host microorganisms, such as, Streptomyces and the Tat pathway therein. Many of the thus-produced proteins are of significant therapeutic value in the pharmaceutical and biochemical industries, particularly when they can be secreted from the host in fully-folded active form. Accordingly, there are further provided the heterologous proteins produced by the Tat secretion pathway using the foregoing methods, and the computer algorithm used to identify the Tat signal sequence and putative substrates.

Description

REFERENCE TO RELATED APPLICATION[0001]This application is a Divisional of U.S. Pat. No. 7,447,595, which claims priority to U.S. Provisional Application Nos. 60 / 364,877, filed Mar. 15, 2002, and 60 / 441,576, filed Jan. 21, 2003, the contents of each of which are herein incorporated by reference.GOVERNMENT INTEREST[0002]This invention was supported in part by Grant Nos. T32GM-007229 from the National Institutes of Health, 0110093U from the American Heart Association, MCB 9816411 from the National Science Foundation and DE-FG02-01ER15169 from the Department of Energy. Accordingly, the Government may have certain rights in this invention.FIELD OF THE INVENTION[0003]This invention comprises a method of analyzing a protein secretion process in certain prokaryotic organisms, and methods for achieving the efficient, controlled production of folded heterologous proteins therefrom.BACKGROUND OF THE INVENTION[0004]Genomics research has led to protein therapeutics that are claiming an increasin...

AI Technical Summary

Benefits of technology

[0016]The present invention studied the alternative twin arginine translocation (Tat) secretory pathway in Streptomyces and other bacterial species. It provides a means for evaluating and identifying putative substrates of the Tat secretory pathway. It also provides a simple way to produce and purify correctly folded heterologous proteins on a large scale using microorganisms, such as, Streptomyces as hosts and the Tat pathway therein. Thus, it still allows for protein purification from extra-cytoplasmic fractions.

[0017]Industrially tractable bacteria have been identified that are estimated to secrete more then 200 proteins via this alternative pathway. Moreover, it has been shown that these organisms efficiently secrete numerous heterologous proteins of interest in their correctly folded conformations by the use of selected signal leader sequences with a Tat motif to direct protein secretion through this alternative pathway. Thus, substrates that are of biotechnological interest are more likely to be efficiently secreted by microorganisms that naturally utilize the Tat pathway, such as Streptomyces strains, providing a mechanism for secretion of a larger number of fully-folded proteins, than through any of the other prokaryotic expression hosts, avoiding many of the problems encountered by the currently used Sec pathway.

[0020]Yet another object of the present invention is the production of desirable heterologous proteins from a Streptomyces bacterium utilizing the Tat pathway as a means of excretion. By fusing a selected signal sequence permitting optimal translocation efficiency to the N-terminus of the protein of interest, theoretically any protein of interest can be produced and secreted effectively. This is crucial in a market in which protein production is already important, and growing, as the pharmaceutical and biotech industries continue to develop new protein-based therapies, while struggling with facile, reliable and economical ways of producing proteins of interest.

Problems solved by technology

By comparison, given the thousands of endogenous proteins inside of the host cell, separation of a protein of interest is very expensive and inefficient.

However, the Sec pathway secretes unfolded proteins, and thus is unable to secrete a heterologously expressed protein that quickly folds in the cytoplasm, or one that has difficulty folding correctly in the external environment.

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