Biochemistry of Proteins

CROSS-LINKERS


See also: Protein modifyers - Buffers - Labeling reagents (biotin)

 

 

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Homobifunctional cross-linkers contain 2 identic chemical reactif groups. Dimeres (but also some tri- and oligomeres) are generally formed besides conjugates of same molecules, or different molecules. Homobifunctional cross-linkers are dedicated mostly for coupling same molecules together or to immobilization, for production and special studies :

  • immobilization of ligands to supports (plates, gels, beads)

  • production of polymeres at big scale (antigens...)

  • reticulation of big molecules / complexes, and membranes

  • design of multimeres for the study of natural polymeres...

Homobifunctional cross-linkers NH2/HNS -- NHS / NH2 (page7...page9)

DSS

Sulfo-DSS (BS3)

DMAI (DMA)

DMPI (DMP)

DMSI (DMS)

DTBP

DSSeb

Sulfo-DSSeb

 

DSS

UP28065A

1g

Sulfo-DSS(BS3)

UP54940A

100mg

UP28065B

5x1g

UP54940B

50mg

A classical homobifunctional amine reactive crosslinker

  • Reacts with NH2 via NHS at pH7-9 forming a stable amide bond

  • 11.4Å linear spacer, very flexible, non cleavable

Water soluble analog of DSS

  • Features of the DSS

  • Soluble directly in aqueous buffer (no need DMSO)

  • Do not cross biological membranes

Dissucinimidyl Suberate

MW 368.4

CAS [68528-80-3]

Bis(Sulfosuccinimidyl) Suberate ester

MW 572.4

CAS [82436-77-9]

Technical Sheet

Applications / Literature

Receptor-protein studies

Immobilisation of IgG on protein A

Cox (1990), Petruzelli (1985), Rashidbaigi (1986), Sawyer (1987)

Technical Sheet

Applications / Literature

Cell Crosslinking biomolecules on cells (Jordan 1996)

In Out-side membrane receptor-protein studies

Bifunctional bioconjugates

Wolf (1994), Locascio-Brown (1990), Terlecky (1996),

Jordan(1996), Sargiacome (1995), Knoller (1991),

Staros (1982), Ward (1985), Souza (1988)

Arylated spacer should be useful when hydrophobic patterns, or when other spacer are though to be short for the desired crosslinking.

 

DMAI(DMA)

UP09962A

1g

DMPI(DMP)

UP362009

100mg

UP09962B

10g

UP36200A

1g

UP36200B

10g

An original alternative to DSS and DSG

  • Reacts with NH2 via imidoesters at pH8-10 forming a charged amide bond

  • Short 8.6Å spacer (6 atoms)

  • Cleavable at pH>10

Slightly longer spacer than DMAI

  • Features of the DMAI

  • Short 9.2Å spacer (7 atoms)

Dimethyl Adipimidate.2HCl

MW 245.1

CAS [14620-72-5]

Dimethyl Pimelimidate.2HCl

MW 259.2

CAS [58537-94-3]

Protein-protein interaction studies

Technical Sheet

Applications / Literature

Protein-protein interaction studies

Hartman (1967)

Technical Sheet

Applications / Literature

Protein confirmation studies Brew (1975)

Schneider (1982)

DMSI(DMS)

UP06633A

1g

DTBP

UP997960

On inquire

UP06633B

10g

Slighly longer spacer than DMPI

  • Features of the DMAI

  • Short 11.0Å spacer (8 atoms)

The cleavable analog of DMSI

  • Features of the DMAI

  • Thiol-cleavable 11.9Å spacer (8 atoms)

Dimethyl Suberimidate.2HCl

MW 259.2

CAS [34490-86-3]

Dimethyl-3,3'-DithioBisPropionamidate.2HCl

MW 309.3

CAS [38285-78-8]

Technical Sheet

Applications / Literature

Protein-protein interaction studies, Darrest (1970)

Wang (1977)

Applications / Literature

Protein-protein interaction studies

Shiudasani (1988), Wang (1974), Labbe (1982), Ruotto (1975)

DSSeb

G9912A

On inquire

Sulfo-DSSeb

G9911A

On inquire

Extended spacer analog of DSS

  • Reacts with NH2 via NHS at pH7-9 forming a stable amide bond

  • 10-C arylated spacer, longer and more flexible than DSS, not cleavable

  • Spacer less immunogenic

The water soluble analog

  • Features of the BSOCOES

  • Soluble directly in aqueous buffer (no need DMSO)

  • Do not cross biological membranes

Bis(Succinimidyl)Sebacate

MW 396.4

Bis(sulfoSuccinimidyl)Sebacate

MW 600.5

Arylated spacer should be useful when hydrophobic patterns, or when other spacer are though to be short for the desired crosslinking.

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Applications / Literature

Membrane receptor studies

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