# Hijacked then lost in translation: the plight of the recombinant host cell in membrane protein structural biology projects

**Authors:** Roslyn M Bill, Tobias von der Haar

PMC · DOI: 10.1016/j.sbi.2015.04.003 · 2015-06-01

## TL;DR

This paper reviews how host cells produce membrane proteins for structural biology, focusing on translation and folding to improve protein yields.

## Contribution

The paper provides new insights into optimizing recombinant membrane protein production by examining host cell quality control mechanisms.

## Key findings

- High-yield membrane protein production depends on host cell resource allocation and protein folding.
- Emerging strategies use host cell biology to improve recombinant protein yields for structural studies.
- Translation and folding processes are critical for successful membrane protein crystallization.

## Abstract

•Membrane protein structural biologists need high-quality protein for crystallisation.•Recombinant proteins are central to the structural biology supply chain.•Understanding quality control in protein production is an emerging trend.•The roles of translation and protein folding in the host cell are examined.

Membrane protein structural biologists need high-quality protein for crystallisation.

Recombinant proteins are central to the structural biology supply chain.

Understanding quality control in protein production is an emerging trend.

The roles of translation and protein folding in the host cell are examined.

Membrane protein structural biology is critically dependent upon the supply of high-quality protein. Over the last few years, the value of crystallising biochemically characterised, recombinant targets that incorporate stabilising mutations has been established. Nonetheless, obtaining sufficient yields of many recombinant membrane proteins is still a major challenge. Solutions are now emerging based on an improved understanding of recombinant host cells; as a ‘cell factory’ each cell is tasked with managing limited resources to simultaneously balance its own growth demands with those imposed by an expression plasmid. This review examines emerging insights into the role of translation and protein folding in defining high-yielding recombinant membrane protein production in a range of host cells.

## Full-text entities

- **Genes:** CAV2 (caveolin 2) [NCBI Gene 858] {aka CAV}, NCSTN (nicastrin) [NCBI Gene 23385] {aka ATAG1874}, HVCN1 (hydrogen voltage gated channel 1) [NCBI Gene 84329] {aka HV1, VSOP}, ASIC1 (acid sensing ion channel subunit 1) [NCBI Gene 41] {aka ACCN2, ASIC, BNaC2}, TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}, GRIN2B (glutamate ionotropic receptor NMDA type subunit 2B) [NCBI Gene 2904] {aka DEE27, EIEE27, GluN2B, MRD6, NMDAR2B, NR2B}, AQP2 (aquaporin 2) [NCBI Gene 359] {aka AQP-2, AQP-CD, NDI2, WCH-CD}, chloramphenicol acetyltransferase [NCBI Gene 8319152], INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, FFAR1 (free fatty acid receptor 1) [NCBI Gene 2864] {aka FFA1R, GPCR40, GPR40}, CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}, NTS (neurotensin) [NCBI Gene 4922] {aka NMN-125, NN, NT, NT/N, NTS1}, hns [NCBI Gene 13905950], CLDN15 (claudin 15) [NCBI Gene 24146], INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC10A2 (solute carrier family 10 member 2) [NCBI Gene 6555] {aka ASBT, IBAT, ISBT, NTCP2, PBAM, PBAM1}, DERL1 (derlin 1) [NCBI Gene 79139] {aka DER-1, DER1, derlin-1}, AGTR1 (angiotensin II receptor type 1) [NCBI Gene 185] {aka AG2S, AGTR1B, AT1, AT1AR, AT1B, AT1BR}, HCN2 (hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2) [NCBI Gene 610] {aka BCNG-2, BCNG2, EIG17, FEB2, GEFSP11, HAC-1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, ANO1 (anoctamin 1) [NCBI Gene 55107] {aka DOG1, INDMS, MYMY7, ORAOV2, TAOS2, TMEM16A}, BEST1 (bestrophin 1) [NCBI Gene 7439] {aka ARB, BEST, BMD, Best1V1Delta2, RP50, TU15B}, MGAT1 (alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase) [NCBI Gene 4245] {aka GLCNAC-TI, GLCT1, GLYT1, GNT-1, GNT-I, GnTI}
- **Species:** Aequorea victoria (species) [taxon 6100], Spodoptera frugiperda (fall armyworm, species) [taxon 7108], Gallus gallus (bantam, species) [taxon 9031], Komagataella pastoris (species) [taxon 4922], Escherichia coli (E. coli, species) [taxon 562], Escherichia coli BL21(DE3) (strain) [taxon 469008], Homo sapiens (human, species) [taxon 9606], Pontellina plumata (species) [taxon 239963], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Cytomegalovirus (genus) [taxon 10358]
- **Cell lines:** C43 — Mus musculus (Mouse), Hybridoma (CVCL_C5DC), HEK293S — Homo sapiens (Human), Transformed cell line (CVCL_A784), insect — Trichoplusia ni (Cabbage looper), Spontaneously immortalized cell line (CVCL_C190), HEK293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), T-REx-293 — Homo sapiens (Human), Transformed cell line (CVCL_D585), HEK293T — Homo sapiens (Human), Transformed cell line (CVCL_0063), HEK293F — Homo sapiens (Human), Transformed cell line (CVCL_6642)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4521084/full.md

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Source: https://tomesphere.com/paper/PMC4521084